1. Cell Biology
  2. Developmental Biology

Murine endothelial serine palmitoyltransferase 1 (SPTLC1) is required for vascular development and systemic sphingolipid homeostasis

  1. Andrew Kuo
  2. Antonio Checa
  3. Colin Niaudet
  4. Bongnam Jung
  5. Zhongjie Fu
  6. Craig E Wheelock
  7. Sasha A Singh
  8. Masanori Aikawa
  9. Lois E Smith
  10. Richard L Proia
  11. Timothy Hla  Is a corresponding author
  1. Vascular Biology Program, Boston Children’s Hospital, Department of Surgery, Harvard Medical School, United States
  2. Unit of Integrative Metabolomics, Institute of Environmental Medicine, Karolinska Institute, Sweden
  3. Department of Ophthalmology, Boston Children's Hospital, Harvard Medical School, United States
  4. Department of Respiratory Medicine and Allergy, Karolinska University Hospital, Sweden
  5. Gunma University Initiative for Advanced Research, Gunma University, Japan
  6. Center for Interdisciplinary Cardiovascular Sciences, Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, United States
  7. Genetics and Biochemistry Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, United States
https://doi.org/10.7554/eLife.78861
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Cite this article
  1. Andrew Kuo
  2. Antonio Checa
  3. Colin Niaudet
  4. Bongnam Jung
  5. Zhongjie Fu
  6. Craig E Wheelock
  7. Sasha A Singh
  8. Masanori Aikawa
  9. Lois E Smith
  10. Richard L Proia
  11. Timothy Hla
(2022)
Murine endothelial serine palmitoyltransferase 1 (SPTLC1) is required for vascular development and systemic sphingolipid homeostasis
eLife 11:e78861.
https://doi.org/10.7554/eLife.78861
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Abstract

Serine palmitoyl transferase (SPT), the rate-limiting enzyme in the de novo synthesis of sphingolipids (SL), is needed for embryonic development, physiological homeostasis, and response to stress. The functions of de novo SL synthesis in vascular endothelial cells (EC), which line the entire circulatory system, are not well understood. Here, we show that the de novo SL synthesis in EC not only regulates vascular development but also maintains circulatory and peripheral organ SL levels. Mice with an endothelial-specific gene knockout of SPTLC1 (Sptlc1 ECKO), an essential subunit of the SPT complex, exhibited reduced EC proliferation and tip/stalk cell differentiation, resulting in delayed retinal vascular development. In addition, Sptlc1 ECKO mice had reduced retinal neovascularization in the oxygen-induced retinopathy model. Mechanistic studies suggest that EC SL produced from the de novo pathway are needed for lipid raft formation and efficient VEGF signaling. Post-natal deletion of the EC Sptlc1 also showed rapid reduction of several SL metabolites in plasma, red blood cells, and peripheral organs (lung and liver) but not in the retina, part of the central nervous system (CNS). In the liver, EC de novo SL synthesis was important for acetaminophen-induced rapid ceramide elevation and hepatotoxicity. These results suggest that EC-derived SL metabolites are in constant flux between the vasculature, circulatory elements, and parenchymal cells of non-CNS organs. Taken together, our data point to the central role of the endothelial SL biosynthesis in maintaining vascular development, neovascular proliferation, non-CNS tissue metabolic homeostasis, and hepatocyte response to stress.

Editor's evaluation

This study clearly defines an important role for SPTLC1 in vascular endothelial cell development. The data presented herein will help promote our understanding of endothelial cell metabolism and how metabolic disorders can cause vascular abnormalities.

https://doi.org/10.7554/eLife.78861.sa0

Introduction

Sphingolipids (SL), which comprise ~10–20% of total cellular lipids, are involved in wide range of biological processes. Complex membrane SL, sphingomyelin (SM) and glycosphingolipids, are enriched in lipid rafts and caveolae, which provide an optimal platform for intracellular signaling and cell-cell interactions (van Meer et al., 2008). In contrast, the secreted SL, sphingosine-1-phosphate (S1P), acts as a ligand for G-protein coupled receptors (S1PR1-5) which regulate many physiological and pathological functions (Proia and Hla, 2015). While SL can be derived from dietary sources, most cellular SL are synthesized via the de novo pathway. This pathway is initiated in the endoplasmic reticulum by the condensation of serine and fatty acyl-CoA to generate 3-ketosphinganine by the serine palmitoyltransferase (SPT) enzyme complex. The product, 3-ketosphinganine, is further converted into dihydrosphingosine (dhSph), dihydroceramide (dhCer), and ultimately ceramide (Cer), which is a substrate for the production of complex SL and metabolites such as sphingosine (Sph) and S1P (Merrill, 2002). The SPT complex, which is composed of long chain subunit 1 (SPTLC1), subunit 2/3 (SPTLC2/3) and small subunit A/B (SPTSSA/B), catalyzes the rate-limiting step in the de novo SL biosynthetic pathway (Han et al., 2009). Absence of any of the subunits abolishes the enzymatic activity of SPT, which is required for normal embryonic development in mice (Hojjati et al., 2005). In addition, SPT enzyme activity is controlled by interaction with ORMDL proteins, which respond to extracellular and cell-intrinsic cues to regulate the flux of SL synthesis by the de novo pathway (Siow et al., 2015; Han et al., 2019).

The involvement of de novo SL biosynthetic pathway in organ function and diseases have been deduced from genome wide association studies and mouse genetic models. Mutations in the SPTLC1 gene are associated with peripheral neuronal dysfunction including hereditary sensory neuropathy type 1 (HSAN1) (Bejaoui et al., 2001; Dawkins et al., 2001), childhood amyotrophic lateral sclerosis (ALS) (Mohassel et al., 2021) and macular telengectasia type-2 (Gantner et al., 2019). Sptlc2 haploinsufficiency in macrophages causes reduction of circulating SM and enhancement of reverse cholesterol transport in murine genetic models (Chakraborty et al., 2013), suggesting the requirement of this pathway in maintaining systemic SL homeostasis. Loss of function of the SPT complex in hepatocytes reduces SM in the plasma membrane and suppresses the expression of E- and N-cadherin, adherens junction constituents (Li et al., 2016), highlighting the importance of this pathway in maintaining proper plasma membrane function. Collectively, these data reveal the plethora of cell-type-specific functions of SL derived from the de novo pathway.

Endothelial cells (EC) line the inner layer of the circulatory system and mediate vascular tone control, barrier integrity, oxygen supply, immune cell trafficking and waste removal. The vasculature of the central nervous system (CNS), which includes the brain and retina, is unique in that EC help form a highly selective barrier for circulatory metabolites. Indeed, EC in CNS forms a specialized structure between the blood and the tissue, known as the blood brain barrier (BBB) and blood retinal barrier (BRB) that consist of cellular compartments including EC, pericytes, and neural cells (astrocytes, glia and neurons). SL metabolites, originally isolated from brain due to their relative abundance, are critical for CNS development, physiology and disease (Olsen and Færgeman, 2017). Metabolism of some lipids such as cholesterol are compartmentalized in CNS and non-CNS tissues (Orth and Bellosta, 2012). Whether SL metabolism in CNS and non-CNS organs is compartmentalized and the role of SL in organotypic vascular beds is not known.

Our current knowledge about SL metabolism in EC has been centered around S1P, a key lipid mediator needed for developmental and pathological angiogenesis, and Cer, a mediator of stress responses (Cartier and Hla, 2019; Jernigan et al., 2015). Activation of S1P signaling in the EC S1PR1 suppresses vascular endothelial growth factor (VEGF) dependent vascular sprouting and maintains barrier integrity, resulting in stable and mature vessels (Jung et al., 2012; Gaengel et al., 2012). Upon irradiation, Cer aggregate to form Cer-enriched membrane domains within the cell membrane, which regulate physicochemical properties of membranes, leading to apoptosis and capillary leak (Kolesnick and Fuks, 2003). Moreover, VEGFR2 has been shown to colocalize with SL enriched lipid rafts on the plasma membrane and impact VEGF-induced intracellular signal transduction processes (Laurenzana et al., 2015). These results suggest that multiple SL metabolites regulate vascular development (angiogenesis), homeostasis and diseases. Recently, it was that EC-specific deletion of Sptlc2 results in lower blood pressure and reduced plasma Cer, implying the protective function of de novo SL biosynthetic pathway in vascular disease (Cantalupo et al., 2020). However, the role of de novo SL biosynthetic pathway in metabolic flux of SL metabolites in various tissue compartments and vascular development is not known.

To address these questions, we generated a mouse model in which de novo synthesis of SL can be abolished by tamoxifen-induced Sptlc1 gene deletion in endothelial cells (Sptlc1 ECKO). Sptlc1 ECKO mice exhibited delayed retinal vascular development and reduced pathological angiogenesis in an oxygen-induced retinopathy model. This is due, at least in part, to defects in endothelial lipid rafts and impaired VEGF signaling. Moreover, Sptlc1 ECKO mice showed rapid decline of many SL, including dhSph, dihydrosphingosine-1-phosphate (dhS1P) and Cer in plasma and red blood cells (RBC), demonstrating SL metabolic flux from EC to circulation. SL content of peripheral tissues such as lung and liver were also reduced upon Sptlc1 EC deletion. Reduced Cer levels in Sptlc1 ECKO mice protected against acetaminophen-induced hepatoxicity, suggesting the functional importance of EC SL supply in liver response to stress. Collectively, our data not only demonstrate the role of de novo synthesis of SL during vascular development, but also reveal a novel function of EC as a source to provide SL to the circulation and peripheral tissues for their proper functions and response to stress.

Results

Endothelial SPT enzyme supplies sphingolipids to vascular and non-vascular cells in the lung

We generated a mouse strain in which Sptlc1 floxed mice are crossed with tamoxifen-inducible VE-cadherin Cre recombinase mice (Sptlc1 ECKO, Figure 1—figure supplement 1A). Mice were administered tamoxifen at 6 weeks of age and followed for 10 weeks. We did not observe any changes in body weight or gross abnormalities (Figure 1—figure supplement 1B). Blood chemistry analyses indicated that Sptlc1 ECKO mice have normal liver enzyme levels, kidney function and blood chemistry (Figure 1—figure supplement 1C). To determine the efficiency and specificity of Sptlc1 gene deletion, we prepared EC (CD31+; CD45-) and non-EC (CD31-) from single-cell suspensions isolated from enzymatically digested lung tissues (Figure 1A). Flow cytometry analyses showed that isolated EC population was ~90% pure and non-EC population contains <10% of contaminating CD31+ cells (Figure 1B). SPTLC1 expression was reduced markedly (~80%) in Sptlc1 ECKO endothelium specifically (Figure 1C–E). In contrast, SPTLC1 expression in bone marrow which has low EC content did not show differences in WT vs. Sptlc1 ECKO (Figure 1—figure supplement 2). These results demonstrate that SPTLC1 expression is almost completely suppressed in the vascular endothelium of Sptlc1 ECKO mice.

Figure 1 with 4 supplements see all
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Ablation of Sptlc1 in EC reduces SL content in both EC and non-EC cell population of the lung.

(A) Scheme of lung EC and non-EC isolation procedure used in this figure. (B) Representative flow cytometry analysis for determination of lung non-EC and EC population purities. Non-EC is identified as CD45+/-; CD31- cells (Q1 + Q4). EC is identified as CD45-; CD31 + cells (Q3) (n=4 for both EC and non-EC). (C) EC and non-EC from Ctrl and Sptlc1 ECKO lungs were analyzed by Western Blotting for SPTLC1 and eNOS expressions. eNOS was used as an EC marker to demonstrate purity of each population. β-actin was used as an internal control. Relative fold change of SPTLC1 to Ctrl in EC and non-EC population were normalized to β-actin and quantified in (D) an (E) (n=3 for both genotypes). SL content in Ctrl and Sptlc1 KO EC was determined by LC-MS/MS, including dhC16-Cer, dhSph, dhS1P, Sph and S1P in (F), total Cer content in (G), and SM in (H) (n=5 for Ctrl EC, n=4 for Sptlc1 KO EC). SL content in Ctrl and Sptlc1 KO non-EC was determined by LC-MS/MS, including dhC16-Cer, dhSph, dhS1P, Sph, and S1P in (I), total Cer content in (J), and total SM content in (K) (n=5 for Ctrl non-EC, n=4 for Sptlc1 KO non-EC). Values of lipidomic results can be accessed in Figure 1—source data 1. Data are expressed as mean ± SD. Statistical significance was determined by unpaired t test. *p<0.05; **p<0.01. ***p<0.001. ns, non-significant.

Figure 1—source data 1

Levels of dhC16-Cer, dhSph, dhS1P, Sph, S1P, Cer, and SM in lung EC and non-EC populations of Ctrl and Sptlc1 ECKO mice.

https://cdn.elifesciences.org/articles/78861/elife-78861-fig1-data1-v3.xlsx
Figure 1—source data 2

Original blots of EC and non-EC from Ctrl and Sptlc1 ECKO lungs.

https://cdn.elifesciences.org/articles/78861/elife-78861-fig1-data2-v3.zip

We next measured SL metabolites in isolated lung EC from Sptlc1 ECKO mice by LC-MS/MS. SL species in the de novo biosynthetic pathway, namely, dhSph, C16-dihydroceramide (dhC16-Cer) were markedly reduced (Figure 1F). In addition, Sph, S1P and dhS1P were reduced. Cer species, including C16:0, C22:1, C22:0, C24:0, C24:1, and C26:0, were also reduced, resulting in decreased total EC Cer levels (Figure 1G, Figure 1—figure supplement 3A). Moreover, SM species, including C16:0, C22:0, C24:0, C26:1, C26:0 SM, were reduced, resulting in decreased total EC SM content (Figure 1H, Figure 1—figure supplement 3B). These data show that lack of SPTLC1 subunit leads to marked reduction in many SL metabolites of EC.

We noticed that dhSph, S1P and several Cer species were significantly reduced in non-EC populations isolated from lungs of Sptlc1 ECKO mice while some SL (dhC16-Cer, dhS1P, Sph and SM) were unaffected (Figure 1I–K, Figure 1—figure supplement 3C, D). Given that non-EC population contained less than 10% of CD31+ cells (Figure 1B), the reduction is unlikely to be caused by EC contamination. Instead, this finding suggests that EC-derived SL metabolites are transferred to non-EC parenchymal cells in the lung.

EC SPT regulates retinal vascular development and pathological neovascularization

We next investigated whether EC SPT is important for vascular development. Vascular network develops in the murine retina after birth and is fully formed by postnatal day 30 (P30) (Rust et al., 2019). Sptlc1 ECKO mice exhibited a lower retinal vascular density and delayed radial expansion of retinal vascular network at P6 compared to controls (Figure 2A–C) while pericyte coverage was not altered (Figure 2D and E). Proliferation of retinal EC was reduced in Sptlc1 ECKO mice as indicated by phosphorylated histone H3 staining (Figure 2F and G). Tip cells, which require active VEGF signaling during vascular development, was markedly reduced in Sptlc1 ECKO mice, as indicated by ESM1 staining of developing retina (Figure 2F and H). Reduced tip cell formation and proliferation of stalk cells likely led to the abnormalities in retinal vascular development. The deeper vascular plexus, which begins to form ~P9 by vertical expansion of vascular sprouts from the superficial vascular network, also showed marked developmental delay in Sptlc1 ECKO mice compared to controls (Figure 2I–K). However, expression of EC proteins important for BRB formation, including LEF1 (a key transcription factor involved in canonical Norrin/Wnt signaling), TFRC (transferrin receptor C), and CLDN5 (Claudin-5, a tight junction protein) were not altered at P6, suggesting that retinal EC organotypic specialization is not affected in the absence of SPT (Figure 3A–E). Interestingly, MFSD2A, a lysophospholipid transporter that suppresses transcytosis in EC, was upregulated in the retinal arteries of Sptlc1 ECKO retina (Figure 3D and F). The delayed vascular developmental phenotype was normalized at P15 (Figure 3—figure supplement 1). We surmise that SL synthesized by other cells of the retina or derived from circulatory sources rescued the Sptlc1 ECKO phenotype in the vasculature at later stages of development. Together, these results suggest that active SPT function, which supplies SL in the endothelium is needed for normal vascular development.

Figure 2
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Retinal vascular development is delayed in the absence of Sptlc1 in EC.

(A) Retinal vascular plexus at P6 of Ctrl and Sptlc1 ECKO mice were immunostained with Isolectin-B4 (IB4). Vascular density and outgrowth were quantified in (B) and (C) (n=16 for Ctrl, n=9 for Sptlc1 ECKO). (D) Pericytes were immunostained with NG2 and pericytes coverage was quantified by NG2+/IB4+ area as shown in (E) (n=8 for Ctrl, n=6 for Sptlc1 ECKO). (F) Proliferating cells and tip cells were immunostained with phospho-histone H3 (pHH3) and ESM1 respectively. ERG immunostaining was served as an EC marker. White arrows indicate pHH3+/ERG+ cells and quantified in (G) (n=8 for Ctrl, n=6 for Sptlc1 ECKO). Tip cells were quantified by ESM1+/ERG+ cells as shown in (H) (n=14 for Ctrl, n=8 for Sptlc1 ECKO). (I) Retinal vascular plexus at P10 of Ctrl and Sptlc1 ECKO mice were immunostained with IB4. Representative images of total and inner plexus were shown and vascular density was quantified in (J) and (K) (n=4 for Ctrl, n=4 for Sptlc1 ECKO). Data are expressed as mean ± SD. Statistical significance was determined by unpaired t test. *p<0.05; **p<0.01; ***p<0.001. ns, nonsignificant. Scale bar in (A): 500 μm, in (D) and (F): 100 μm, in (I) and (L): 500 μm.

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Blood-retina barrier (BRB) protein expressions are not reduced in the retina of Sptlc1 ECKO mice.

(A) BRB associated proteins including LEF1 and TFRC in Ctrl and Sptlc1 ECKO P6 retina were immunostained and quantified by colocalization with IB4 staining shown in (B) and (C) (n=4 for Ctrl, n=5 for Sptlc1 ECKO). (D) Tight junction protein, CLDN5 in Ctrl and Sptlc1 ECKO P6 retina were immunostained and quantified by colocalization with IB4 staining shown in (E) (n=3 for Ctrl, n=7 for Sptlc1 ECKO). BRB specific protein, MFSD2A, in Ctrl and Sptlc1 ECKO P6 retina were immunostained and quantified by colocalization with IB4 staining shown in (F) (n=3 for Ctrl, n=7 for Sptlc1 ECKO). Arterial and venous regions are marked as ‘A’ and ‘V’. Data are expressed as mean ± SD. Statistical significance was determined by unpaired t test. *p<0.05; ns, non-significant. Scar bars, 100 μm.

Oxygen-induced retinopathy (OIR) is a widely used murine disease model to investigate pathological neovascularization during retinopathy of prematurity, diabetic retinopathy and wet form of age-related macular degeneration (Smith et al., 1994; Campochiaro, 2013). VEGF produced by Müller glia and astrocytes is a major contributor to pathological vascular tuft formation in this model (Weidemann et al., 2010). We used this OIR model in WT and Sptlc1 ECKO mice to determine the role of EC-derived SL metabolites in pathological angiogenesis. Tamoxifen was administered at P1-P3 to induce Sptlc1 deletion and mouse pups were exposed to 75% O2 from P7-P12 (Figure 4A). This hyperoxia environment causes capillary dropout (vaso-obliteration) due in part to suppression of VEGF production (Smith et al., 1994). In the absence of EC de novo SL synthesis, vascular dropout was exacerbated at P10 and P12, resulting in reduced vascular network density and increased avascular areas (Figure 4B–G). These results suggest that reduced SL de novo synthesis in EC led to reduced VEGF sensitivity of EC resulting in higher vascular dropout. Upon return to normoxia, avascular zones become severely hypoxic and induce high levels of VEGF which drive the formation of vascular tufts. To examine the role of EC Sptlc1 in the neovascular phase of OIR, we induced EC Sptlc1 deletion at P12 which is the beginning of the retinal hypoxia in this animal model (Figure 4H). With this timed gene deletion strategy, we observed significant attenuation of pathological neovascularization in Sptlc1 ECKO mice at P17 (Figure 4I and J). In addition, vaso-obliterated regions were larger in Sptlc1 ECKO mice (Figure 4I and K). Collectively, the results from the OIR model indicate that de novo synthesis of SL in EC determine the pathological phenotypes in the retinal vasculature (vessel dropout and pathological vascular tuft formation), likely due to reduced VEGF responsiveness.

Figure 4
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Sptlc1 ECKO mice show enhanced vaso-obliteration and reduced neovascularization in oxygen induced retinopathy model.

(A) Schematic of timeline for tamoxifen treatment, oxygen challenge and tissue collection used from (B) to (G). (B) P10 retinas of control and Sptlc1 ECKO mice were immunostained with IB4 and smooth muscle actin (SMA). Vascular density and vaso-obliteration (dashed line area) were quantified in (C) and (D) (n=7 for Ctrl, n=3 for Sptlc1 ECKO). (E) P12 retinas of control and Sptlc1 ECKO mice were stained with IB4 and SMA. Vascular density and vaso-obliteration (dashed line area) were quantified in (F) and (G). (n=10 for Ctrl, n=11 for Sptlc1 ECKO). (H) Schematic of timeline for tamoxifen treatment, oxygen challenge and tissue collection used from (I) to (K). Note that tamoxifen was administered after 75% O2 challenge. (I) P17 retinas of control and Sptlc1 ECKO mice were immunostained with IB4 and SMA. Neovascularization (white area) and vaso-obliteration (dashed line area) were quantified in (J) and (K) (n=15 for Ctrl, n=6 for Sptlc1 ECKO). Data are expressed as mean ± SD. Statistical significance was determined by unpaired t test. *p<0.05; **p<0.01, ***p<0.001. ns, non-significant. Scale bars, 500 μm.

EC SPT maintains lipid rafts and enables optimal VEGF signaling

To demonstrate that VEGF signaling is impaired in Sptlc1 KO EC of the retina, exogenous VEGF-A was administered to P6 mouse pups via intraocular injection. In concurrence with published reports (Eilken et al., 2017; Gerhardt et al., 2003), VEGF-treated capillaries in the vascular front were dilated with increased EC numbers as depicted by ERG staining 4 hr post-injection (Figure 5A–B). These phenotypes were attenuated in Sptlc1 ECKO retinas, suggesting that VEGF responsiveness in EC is attenuated in the absence of de novo SL synthesis (Figure 5A–C). Moreover, exogenous VEGF-A induced ESM1 expression in the plexus regions of the vasculature (ectopic tip cells) (Rocha et al., 2014). Supporting our hypothesis, the number of ESM1+ ectopic tip cells was reduced in Sptlc1 ECKO retinas compared to the Ctrl retinas (Figure 5A–C). Collectively, our results indicate that SPTLC1 in retinal endothelium contributes to proper VEGF responsiveness.

Figure 5
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Loss of SPT activity in EC impairs VEGF signaling via modulation of lipid rafts.

(A) P6 retinas of control and Sptlc1 ECKO mice 4 hr post intraocular administration of mouse VEGF-A (50 ng/retina) or vehicle (PBS) were immunostained with ESM1, ERG and IB4. ERG numbers in the vascular front regions (dashed line area) were quantified in (B). Asterisks indicate dilated vessel area. ESM1+/ERG+ cells in the vascular front and capillary plexus (outside of dashed line area) were quantified in (C) (n=8 for Ctrl, n=8 for Sptlc1 ECKO). Arrows indicate ectopic tip cells induced by VEGF treatment in capillary plexus regions. (D) HUVECs treated with Myriocin (Myr), dhSph, Sph and Cer followed by 5 min VEGF-A (50 ng/mL) were analyzed by western blotting for total and phospho-ERK. (E) Relative fold change to phosphorylation of ERK was first normalized to total ERK then toβ-actin as internal control (n=4). (F) HUVECs treated with Myr, dhSph, and Sph were immunostained with conjugated CTxb to label lipid rafts and VECad to label plasma membrane. Arrows indicate loss of CTXb signal in VECad+ area by Myr treatment. Percentage of CTXb signal colocalization in VECad+ area was quantified in (G) (n=10 in each condition from two independent experiment). Data are expressed as mean ± SD. Statistical significance was determined by unpaired t test. *p<0.05; **p<0.01; ***p<0.001, ns, non-significant. Scale bars in (A): 100 μm. and in (F): 50 μm.

Figure 5—source data 1

Original blots of HUVEC lysates treated with VEGF, Myr and different of SL.

https://cdn.elifesciences.org/articles/78861/elife-78861-fig5-data1-v3.zip

To further demonstrate that VEGF signaling and its downstream target activation are attenuated by loss of SPT activity, human umbilical vein endothelial cells (HUVEC) were treated with Myriocin, an inhibitor of SPT complex, followed by VEGF activation. In agreement with a previous report (Cantalupo et al., 2020), VEGF mediated ERK phosphorylation was attenuated by 72 hr of Myriocin pre-treatment (Figure 5D, lane 1–3). Importantly, 6 hr incubation of dhSph rescued ERK phosphorylation abrogated by Myriocin, suggesting that the de novo synthesis pathway of SL is required for efficient VEGF signaling (Figure 5D, lane 3–4). Supplementation of other SL including Sph and Cer (C18:0) can also restored VEGF-induced ERK phosphorylation from the inhibitory effects of Myriocin (Figure 5D, lane 3, 5, 6).

VEGFR is stabilized and modulated by lipid rafts, lipid microdomains enriched in sterols and SL (Zabroski and Nugent, 2021). Therefore, we tested the hypothesis that loss of SPT activity reduces SL which are needed for lipid raft formation and thereby dampen VEGF signaling. To test this, lipid rafts were detected by fluorescently-labelled Cholera Toxin B (CTXb), which specifically binds to the glycosphingolipid GM1. In HUVEC, Myriocin treatment to inhibit SPT and SL synthesis suppressed the CTXb signal at the plasma membrane (Vascular Endothelial Cadherin (VECad) positive area) (Figure 5F left panels, quantified in G). This suggests that continuous SPT activity is needed to form GM1, a lipid raft constituent in HUVEC. In Myriocin treated cells, exogenous supplementation with dhSph and Sph for 6 hr rescued lipid rafts in the plasma membrane (Figure 5F right panels, quantified in G). Taken together, our in vivo and in vitro mechanistic studies demonstrate that de novo synthesis of SL is necessary for efficient VEGF signaling via modulation of lipid raft formation.

Endothelial SPT activity is critical to maintain circulatory SL metabolic homeostasis

Since the non-EC parenchymal cells isolated from the lungs of Sptlc1 ECKO mice contain reduced levels of SL metabolites (Figure 1I–K), we hypothesized that EC-derived SL are transferred to non-EC parenchymal cells either directly (cell-cell transfer) or indirectly via the circulatory system. We first quantified SL metabolites in plasma isolated from adult Sptlc1 ECKO mice. S1P and dhS1P levels were reduced ~60% in Sptlc1 ECKO (Figure 6A). This reduction is more pronounced than that observed in sphingosine kinase-1 and –2 ECKO (Gazit et al., 2016) and S1P transporter (SPNS2) ECKO mice (Hisano et al., 2012; Mendoza et al., 2012). dhSph, a sphingoid base synthesized in the de novo synthesis pathway, was also reduced significantly (Figure 6A). Moreover, Cer species (C24:1, C24:0, C26:1, and C26:0) were reduced in Sptlc1 ECKO plasma, which resulted in reduction of total Cer in plasma (Figure 6B and C). In contrast, SM species were not altered in the plasma of Sptlc1 ECKO mice (Figure 6D and E). These results indicate that SL de novo synthesis pathway in EC is a significant source of sphingoid bases, their phosphorylated metabolites and Cer in plasma.

Figure 6
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Sptlc1 ECKO displays reduced SL content in circulation.

SL content in plasma from Ctrl and Sptlc1 ECKO mice was determined by LC-MS/MS, including dhC16-Cer, dhSph, dhS1p, Sph and S1P in (A), Cer with different fatty acyl chain length in (B), total Cer content in (C), and SM with different fatty acyl chain length in (D), and total SM in (E) (n=5 for Ctrl, n=3 for Sptlc1 ECKO). SL content in RBC from Ctrl and Sptlc1 ECKO mice was determined by LC-MS/MS, including dhC16-Cer, dhSph, dhS1p, Sph, and S1P in (F), Cer with different fatty acyl chain lengths in (G), total Cer content in (H), and SM with different fatty acyl chain lengths in (I), and total SM in (J) (n=5 for Ctrl, n=3 for Sptlc1 ECKO). Values of lipidomic results can be accessed in Figure 6—source data 1. Data are expressed as mean ± SD. Statistical significance was determined by unpaired t test. *p<0.05; **p<0.01. ns, non-significant.

Figure 6—source data 1

Levels of dhC16-Cer, dhSph, dhS1P, Sph, S1P, Cer, and SM in plasma and RBC of Ctrl and Sptlc1 ECKO mice.

https://cdn.elifesciences.org/articles/78861/elife-78861-fig6-data1-v3.xlsx

RBC, which store and release S1P, are a major contributor of plasma S1P (Pappu et al., 2007). We therefore quantified SL metabolites in RBC of Sptlc1 ECKO mice. Sphingoid bases and their phosphorylated counterparts (dhSph, dhS1P, and S1P) were significantly reduced in Sptlc1 ECKO RBCs (Figure 6F). Cer species (C22:1, C22:0, C24:0, and C26:0) were also reduced (Figure 6G and H). SM species were not altered in RBC of Sptlc1 ECKO mice (Figure 6I and J). These results show that reduction of SL metabolites in EC result in concomitant changes in plasma and RBC pools of SL metabolites. This suggests that SL metabolic flux occurs from EC to plasma and cells in circulation.

We next determined the kinetics of SL reduction in plasma/RBC after the deletion of EC Sptlc1. Tamoxifen was injected at 6 weeks of age to induce deletion of EC Sptlc1 and plasma/RBC SL metabolites were quantified at various times. Rapid reduction of plasma S1P levels observed as early as 1 week and maintained thereafter (Figure 7A). Kinetics of RBC S1P reduction was similar (Figure 7B), suggesting that EC SL metabolites are rapidly secreted into plasma and that RBC and plasma SL pools are in rapid equilibrium under physiological conditions.

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Rapid reduction of SL content in circulation upon Sptlc1 deletion.

S1P levels from plasma and RBC of Ctrl and Sptlc1 ECKO mice were measured upon Sptlc1 deletion over time as shown in (A) and (B) (n=3–8 for Ctrl in each time point, n=2–8 for Sptlc1 ECKO in each time point). (C) Plasma from Ctrl and Sptlc1 ECKO mice were fractionated by HPLC (Bio-Rad) into HDL (ApoM enriched), Lipoprotein Free (LPF) (Albumin enriched). S1P levels in each fraction, including total plasma were measured by LC-MS/MS (n=3 for Ctrl, n=3 for Sptlc1 ECKO). SL content from plasma samples of Ctrl and postnatal (P1–P3) deletion of Sptlc1 in EC was measured at P14, P21 and P28 by LC-MS/MS. Species measured are as followed: S1P (D), dhS1P (E), Sph (F), dhSph (G), dhCer (H), total Cer (I), and total SM (J) (n=3–7 for Ctrl in each age, n=4 for Sptlc1 ECKO in each age). Data are expressed as mean ± SD. Statistical significances in (A) and (B) were determined by one-way ANOVA test. Values of lipidomic results can be accessed in Figure 7—source data 1. Statistical significances in (C)-(G) were determined by unpaired t test. *p<0.05; **p<0.01; ***p<0.001. ns, non-significant.

Figure 7—source data 1

Levels of dhC16-Cer, dhSph, dhS1P, Sph, S1P, Cer, and SM in plasma and RBC of Ctrl and Sptlc1 ECKO mice.

https://cdn.elifesciences.org/articles/78861/elife-78861-fig7-data1-v3.xlsx

Plasma S1P is bound to two chaperones, namely Apolipoprotein M (ApoM) on HDL, and albumin in the lipoprotein free fraction (LPF) (Murata et al., 2000). ApoM and albumin levels were not altered in Sptlc1 ECKO plasma (Figure 7—figure supplement 1). By fractionation of plasma using fast protein liquid chromatography, we determined that ApoM bound S1P was not affected while albumin bound S1P in the LPF was significantly reduced in Sptlc1 ECKO mice (Figure 7C). Since albumin bound S1P is less stable (Fleming et al., 2016), released S1P from RBC or EC first bind to albumin, followed by stable interaction with ApoM. Nevertheless, these data suggest that EC SPT-derived S1P is secreted into plasma and equilibrates rapidly with RBC storage pools.

To determine whether the de novo synthesis of SL in EC also contributes to circulatory pools of SL species in early postnatal mice, we deleted EC Sptlc1 from P1-P3 followed by measurement of plasma SL metabolites. Sphingoid bases and phosphorylated derivatives (dhSph, Sph, S1P, dhS1P) showed significant reduction from P14 to P28 in Sptlc1 ECKO mice (Figure 7D–G). In contrast, plasma dhCer, Cer and SM were not changed (Figure 7H–J, Figure 7—figure supplement 2). Differential reduction in SL metabolites in plasma could be due to contributions from non-EC sources, such as the diet and metabolic flux from other cell types at different ages. Together, these results suggest that EC actively provide SL metabolites to circulation postnatally.

SPT in EC supplies sphingolipids in liver and lung but not retina

We examined whether EC SPT enzyme loss affects SL metabolite levels in various organs. We analyzed the liver, lung, and retina because these organs are supplied by vessels with specialized organotypic endothelium (Potente and Mäkinen, 2017). The liver contains sinusoidal EC while lung vasculature is lined by EC specialized for gas exchange. In contrast, the retinal vasculature is lined by CNS-type endothelium which contains numerous tight junctions and specialized transporters with minimal transcytotic vesicles (Andreone et al., 2017). DhSph, a direct product of the de novo SL biosynthetic pathway was significantly reduced in lung and liver of Sptlc1 ECKO mice (Figure 8A and D). In contrast, S1P and Sph levels in these tissues were not reduced (Figure 8A and D). Cer content was reduced about 30–50% in both organs from Sptlc1 ECKO mice with C24:0 and C24:1 Cer species exhibiting largest changes (Figure 8B, C, E and F). These results suggest that EC supply SL metabolites from the de novo pathway into circulation which then equilibrates with liver and lung SL pools. We also measured SL content of retina, a CNS organ system. In sharp contrast to lung and liver, none of the SL metabolites were altered by lack of EC SPT (Figure 8G–H). These results reveal that the SL metabolic flux from EC to adjacent tissues only occurs in circulation and non-CNS organs such as the lung and the liver but not in the retina, which is part of the CNS.

Figure 8
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Sptlc1 ECKO mice exhibit reduced SL content in peripheral but not CNS organs.

SL content from adult liver homogenate of Ctrl and Sptlc1 ECKO adult mice was measured by LC-MS/MS, including dhCer, dhSph, dhS1P, Sph and S1P (A), Cer with different fatty acyl chain length (B) and total Cer (C) (n=3 for Ctrl, n=3 for Sptlc1 ECKO). SL content from adult lung homogenate of Ctrl and Sptlc1 ECKO mice was measured by LC-MS/MS, including dhCer, dhSph, dhS1P, Sph, and S1P (D), Cer with different fatty acyl chain length (E) and total Cer (F) (n=3 for Ctrl, n=3 for Sptlc1 ECKO). SL content from P28 retina homogenate of Ctrl and Sptlc1 ECKO mice were measured by LC-MS/MS, including dhCer, dhSph, dhS1P, Sph, and S1P (G), Cer with different fatty acyl chain length (H) and total Cer (I) (n=5 for Ctrl, n=4 for Sptlc1 ECKO). Values of lipidomic results can be accessed in Figure 8—source data 1. Data are expressed as mean ± SD. Statistical significance was determined by unpaired t test. *p<0.05.

Figure 8—source data 1

Levels of dhC16-Cer, dhSph, dhS1P, Sph, S1P, Cer, and from lung, liver and retina lysates of Ctrl and Sptlc1 ECKO mice.

https://cdn.elifesciences.org/articles/78861/elife-78861-fig8-data1-v3.xlsx

EC SPT supply of liver sphingolipids influences acetaminophen-induced liver injury

Liver function was normal in Sptlc1 ECKO suggesting that reduced SL metabolites are not critical for hepatic homeostasis. However, chemical stress elevates SL metabolites such as Cer, which are thought to mediate liver injury (Li et al., 2020; Park et al., 2013). To determine if EC derived SL influence hepatocyte function, we examined hepatotoxicity induced by N-acetyl-para-aminophenol (APAP; a.k.a. Acetaminophen/Tylenol) in WT and Sptlc1 ECKO mice. APAP treatment resulted in reduced liver injury (aspartate aminotransferase (AST) levels and liver necrosis) in Sptlc1 ECKO mice compared with controls at early time points (4–8 hr) (Figure 9A–C). Liver SL metabolites were quantified at 8 and 24 hr after APAP administration. Many SL metabolites (dhCer C16:0, dhSph, dhS1P, Sph, S1P, Cer C24:1, and total Cer) were lower in the liver at 8 hr post-APAP but only dhCer C16:0 and dhSph were lower in the Sptlc1 ECKO mice at 24 hr (Figure 9D–I). These data suggest that reduced Cer levels in the liver of Sptlc1 ECKO mice at early stabges to attenuation of APAP-induced liver injury.

Figure 9
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Sptlc1 ECKO mice are protected against APAP-induced hepatoxicity.

AST levels were measured from plasma samples of Ctrl and Sptlc1 ECKO mice after 4, 8, and 24 hr of APAP injection (n=3–8 for Ctrl in each time point, n=3–9 for Sptlc1 ECKO in each time point). (B) Liver sections from Ctrl and Sptlc1 ECKO mice after 0, 8, and 24 hr of APAP administration were stained with hematoxylin and eosin. Representative images were shown and dotted lined areas indicate necrotic region. The percentage of necrotic area in total imaging area was quantified in (C) (n=3–5 for Ctrl in each time point, n=3–5 for Sptlc1 ECKO in each time point. each dot represents average of five images from one mouse). SL content in Ctrl and Sptlc1 ECKO liver after 8 hr of APAP injection was measured by LC-MS/MS, including dhC16-Cer, dhSph, dhS1P, Sph and S1P (E), Cer with different fatty acyl chain lengths (F), total Cer content (G) (n=4 for Ctrl, n=4 for Sptlc1 ECKO). SL content in Ctrl and Sptlc1 ECKO liver after 24 hr of APAP injection was measured by LC-MS/MS, including dhC16-Cer, dhSph, dhS1P, Sph, and S1P (H), Cer with different fatty acyl chain length (I), total Cer content (J) (n=4 for Ctrl, n=5 for Sptlc1 ECKO). (D) GSH levels were measured from liver samples of Ctrl and Sptlc1 ECKO mice after 0, 8, and 24 hr of APAP injection (n=3–6 for Ctrl in each time point, n=3–8 for Sptlc1 ECKO in each time point). Values of lipidomic results can be accessed in Figure 9—source data 1. Data are expressed as mean ± SD. Statistical significance was determined by unpaired t test. *p<0.05. **p<0.01. Scale bar, 1 mm.

Figure 9—source data 1

Levels of dhC16-Cer, dhSph, dhS1P, Sph, S1P, Cer, and from liver lysates of Ctrl and Sptlc1 ECKO mice treated with APAP for 8 and 24 hrs.

https://cdn.elifesciences.org/articles/78861/elife-78861-fig9-data1-v3.xlsx

To determine the mechanisms involved in early protective response to APAP toxicity in Sptlc1 ECKO mice, we examined levels of glutathione (GSH), the main antioxidant that protects from APAP-induced hepatoxicity. Liver GSH levels were elevated in Sptlc1 ECKO mice prior to APAP injection. Even though GSH is diminished after APAP-administration, Sptlc1 ECKO mice still had higher GSH levels than the WT counterparts at 8 hr (Figure 9J). Thus, reduced flux of SL metabolites from EC to liver results in attenuated drug-induced hepatotoxicity via modulation of antioxidant GSH levels. These data reveal that EC-derived SL impact stress response of the hepatocytes and liver injury, thus providing a functional significance of this metabolic pathway.

Discussion

Lipids are derived both from the diet and from biosynthetic routes in organs. Their concentrations in various cells and tissues are regulated stringently to maintain normal physiological functions. The numerous SL species are no exception. Altered SL levels due to mutations in biosynthetic or degradative enzymes lead to embryonic lethality or severe genetic diseases (Hannun and Obeid, 2018). However, SL homeostatic mechanisms in various organ systems is poorly understood. For example, cell types which supply SL in various organ systems are not known. In this study, we show that SPT activity in EC regulates developmental and pathological angiogenesis. We also discover a novel function of EC as a major SL source of circulatory SL species, which determines the SL content of organs (the lung and the liver) and the response of liver hepatocytes to chemical injury.

The SPT enzyme complex catalyzes the first committed step in the de novo SL biosynthetic pathway. This step is highly regulated by ORMDL proteins and other poorly understood mechanisms (Cantalupo et al., 2015; Linn et al., 2001; Siow et al., 2015). Since the vascular EC line blood vessels in all organ systems, we developed and analyzed a mouse genetic model in which Sptlc1, encoding the non-redundant subunit of SPT complex (SPTLC1) is disrupted in a tissue-specific manner using tamoxifen-induced gene deletion. This allowed us to precisely disrupt de novo SL synthesis in EC in a temporally manner. Our results revealed that lack of SPTLC1 protein in EC results in delayed vascular development. This phenotype was caused by reduced EC proliferation and tip cell formation in early angiogenic phases. In contrast, organotypic specialization of the developing vasculature was unaffected. This phenotype some similarities with the loss of VEGFR2 in the endothelium (Zarkada et al., 2015). In addition, in the OIR model, where pathological neovascularization is driven primarily by VEGF, inactivation of SPT activity in EC resulted in larger vaso-obliterated zones and reduced vascular tuft formation, again suggesting impaired VEGF signaling. Furthermore, intraocular administration of VEGF-A revealed that Sptlc1 KO EC show attenuated response. Our in vitro studies in HUVEC demonstrated that SPT activity is necessary to maintain efficient VEGF signaling and its downstream substrate activation via lipid rafts. Supplementation of SL such as dhSph, Sph, and Cer is sufficient to rescue the inhibitory effects caused by Myriocin pretreatment, implicating active metabolic turnover of lipid raft constituents such as GM1. Our conclusion agrees with recent publications which described that the EC deletion of Sptlc2 gene impaired VEGFR2-Akt signaling in vitro in adult arterial vessels (Cantalupo et al., 2020) and that lipid rafts enhance VEGFR2 signal transduction during angiogenesis (Zabroski and Nugent, 2021).

In addition to VEGFR2, endothelial nitric oxide synthase (eNOS) resides in SL-rich membrane domains such as lipid rafts or caveolae, suggesting that SPTLC1 loss of function could lead to modulation of eNOS activity. However, eNOS activity in arterial endothelium was elevated in Sptlc2 ECKO adult mice (Cantalupo et al., 2020). In our Sptlc1 ECKO adult mice, eNOS expressions and activation in lung EC was not altered (Figure 1C and Figure 1—figure supplement 4). We postulate that the discrepancy could results from isoform-selective functions between SPTLC1 and SPTLC2. Alternatively, stage-specific function of the SPT enzyme (early postnatal deletion in our study vs. adult stage deletion) or tissue-specific roles (retina EC vs. aorta EC) could explain these divergent effects of SPTLC1 and SPTLC2 on eNOS.

The decreased vascular development phenotype observed in Sptlc1 ECKO mice does not resemble the hypersprouting phenotype nor is there down-regulation of BRB specific genes in mice that lack S1P receptors in EC (Jung et al., 2012; Yanagida et al., 2020). Mice lacking both sphingosine kinases (Sphk1 and Sphk2) in the endothelium did not display alterations in retinal vascular development (Figure 3—figure supplement 2A, B), suggesting that EC-derived S1P is not involved in this process. Furthermore, 50% reduction of plasma S1P observed in Apom KO mice, similar to what we observed in the plasma of Sptlc1 ECKO mice, exhibit normal developmental angiogenesis in the retina (Figure 3—figure supplement 2C, D). These findings suggest that reduced plasma S1P in Sptlc1 ECKO mice is not the cause of the vascular defects seen in Sptlc1 ECKO mice. Hence, we reasoned that membrane functions of SL metabolites, rather than GPCR-dependent signaling functions of S1P are involved.

Extracellular SL carried by lipoproteins and albuminare taken up by cells and metabolized to generate sphingosine (Nilsson and Duan, 2006). SL can also be degraded extracellularly, followed by cellular uptake of sphingosine (Kono et al., 2006). However, it is not known if SL derived from the de novo pathway are transferred between various cells and tissues. A previous report documented that liver specific KO of Sptlc2 reduces plasma SM and Cer, while Sph, S1P and dhS1P are unaffected (Li et al., 2009). Our findings describe a novel metabolic flux of SL metabolites from EC to the circulatory system and peripheral tissues Moreover, SL species were rapidly reduced in RBC and plasma upon Sptlc1 deletion in EC. The reduction of S1P levels in lipoprotein-free fraction of plasma but not in the HDL fraction of Sptlc1 ECKO mice suggest that EC-derived S1P in the plasma interacts first with albumin, followed by stable interaction with ApoM on HDL.

A pivotal question raised from our results is how various SL species produced in the EC are transferred into plasma and circulatory cells. It has been reported that EC contribute to plasma S1P levels via SPNS2, an S1P transporter (Hisano et al., 2012), which raises the possibility that reduced circulatory SL is due to alterations in EC-derived S1P. We believe that this is not the case because loss of Spns2 led to only minor reduction of plasma S1P levels but not in whole blood (Hisano et al., 2012; Mendoza et al., 2012). In addition, RBC S1P transporter (encoded by Mfsd2b gene) knockout mice show S1P accumulation in RBC and reduction in plasma (Vu et al., 2017). Our results from Sptlc1 ECKO mice shows clear differences from the studies which characterized EC and RBC S1P transporter knockout mice. Having ruled out EC secretion of S1P as a possible mechanism, we next considered direct release of dhSph and Cer from EC into circulation, since such SL metabolites were reduced in Sptlc1 ECKO plasma and RBC. While the existence of transporters for dhSph and Cer species have not been described, we do not believe that sphingoid bases and Cer species are directly secreted from EC into circulation. However, alternative ways of transfer may exist. One possibility is through direct contact of EC with lipoproteins and/or RBC. Given that acid sphingomyelinase and ceramidase activities have been reported in the plasma and RBC (López et al., 2012; Xu et al., 2010), complex SL containing both reduced and unreduced sphingoid bases on the outer leaflet of the EC plasma membrane could be metabolized into Cer and sphingoid bases. SL species such as Sph can be taken up and further metabolized by circulating hematopoietic cells including RBC (Nguyen et al., 2021). An alternative mechanism is that EC release of circulating extracellular vesicles (EV) or exosomes from plasma membranes into circulation. It has been reported that Cer, SM, and glycosphingolipids are enriched in EV (Llorente et al., 2013; Verderio et al., 2018; Akawi et al., 2021). It is thus possible that EV derived from EC can bind to RBC or lipoproteins and SL can be taken up and metabolized.

In addition, we observed reduced SL levels in non-EC and peripheral tissues from Sptlc1 ECKO mice. Specific organs and tissues may have different routes for SL transfer based on the unique barrier properties of the organ-specific endothelium. In the liver, EC form fenestrated capillaries with intercellular gaps and discontinuous basement membrane. This allows plasma and macroparticles, to cross EC barrier efficiently and access hepatocytes (Hennigs et al., 2021). SL exchange could therefore occur in the liver due to the porous nature of the liver sinusoidal endothelium. We postulate that the SL metabolic flux from EC to the plasma followed by hepatocyte uptake could explain the reduced liver SL content observed in Sptlc1 ECKO mice. In the case of lung, pulmonary EC are non-fenestrated with tight junctions in between and serve as a semipermeable barrier separating circulation from lung interstitial spaces. To transport materials through lung capillaries, transcytosis acts as the primary route (Jones and Minshall, 2020). It is known to be mediated by caveolae, a critical vesicular structure, which are plasma membrane invaginations enriched in SL and sterols (Harder and Simons, 1997). We speculate that the SL flux in the lung could be mediated by this process which is affected by loss of EC Sptlc1 gene. This mechanism could account for the reduced lung SL species in Sptlc1 ECKO mice. In contrast, caveolae-mediated transcytosis is minimal in the CNS EC which effectively compartmentalizes metabolism of lipids between the circulation and the CNS parenchyma. Our results show that retina SL species were unaffected by lack of de novo SL biosynthesis in EC. Thus, the strict barrier function of the CNS EC ensures compartmentalization of SL metabolism between the neural retina and circulatory/vascular elements.

Finally, we show that Sptlc1 ECKO liver is protected against acetaminophen-induced hepatotoxicity. Increased GSH levels in Sptlc1 ECKO liver suggests that glutathione synthesis, a primary detoxification agent of APAP, may be involved in mediating the protective phenotype. It remains to be determined whether hepatic SL levels regulate GSH levels directly or indirectly. We speculate that lack of SPT activity in EC may allow the unused serine to be converted to GSH since serine is a source of glycine and cysteine used to synthesize glutathione (Zhou et al., 2017). Nevertheless, our results show that SL provided by EC is needed for APAP-induced hepatotoxicity. Recently, Cer species increases has been reported to be involved in drug induced liver injury models in mice (Li et al., 2020). Our liver lipidomic results further suggest a delayed accumulation of Cer in Sptlc1 ECKO mice upon APAP treatment (Figure 8E and H), which correlates with its protective phenotype at early time points. It is worth noting that administration of Fumonisin B1 (FB1), a Cer synthase inhibitor, does not alleviate APAP-induced liver damage (Park et al., 2013). FB1 pretreatment reduces Cer content in the liver while accumulating dhSph, which is in contrast of what we observed in Sptlc1 ECKO liver. Future experiments with myriocin, a direct inhibitor of SPT complex, would be warranted to determine the potential role of dhSph during APAP-induced liver injury.

In conclusion, our studies suggest that de novo SL synthesis pathway in EC is needed for normal and pathological angiogenesis. This is partially due to impaired VEGF responsiveness via modulation of lipid raft formation (Figure 10A). Secondly, we also reveal a novel function of the endothelium as a source of SL metabolites in circulation, lung and liver but not the retina (Figure 10B). This EC-derived SL flux mechanism may be impaired in EC dysfunction, a common mechanism in many cardiovascular and cerebrovascular diseases.

Figure 10
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Graphic abstract summarizing major findings of the study.

(A) Abrogation of SPT activity in EC leads to reduction of SL content, causing EC-intrinsic effects including disruption of lipid rafts. This alteration impairs VEGF-responsiveness, resulting in delayed developmental and pathological angiogenesis. (B) Our studies also reveal that loss of SPT activity in EC exhibit EC-extrinsic effects, where rapid reduction of several SL metabolites in plasma, red blood cells and peripheral organs (lung and liver) but not in the retina, part of the CNS.

Materials and methods

Mouse strains

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Sptlc1fl/fl mice were generated as previously described (Alexaki et al., 2017). Endothelial specific deletion of Sptlc1(Sptlc1 ECKO) were generated by intercrossing Sptlc1fl/fl mice with Cdh5-Cre-ERT2 strain (Sörensen et al., 2009). Sptlc1 ECKO mice used in the experiments were Sptlc1fl/fl carrying one Cdh5-ERT2-Cre allele. Controls were littermate Sptlc1fl/fl mice. To identify Sptlc1fl/fl allele and WT, the following primers were used: 5’-GGG TTC TAT GGC ACA TTT GGT AAG-3’ (forward primer), and 5’-CTG TTA CTT CTT GCC AGT GGA C-3’ (reverse primer), generating products of 350 bp for WT and 425 bp for Sptlc1fl/fl allele (Alexaki et al., 2017). The Cdh5-Cre-ERT2 allele was detected by PCR with the following primers: 5’-TCC TGA TGG TGC CTA TCC TC-3’ (forward primer), and 5’-CCT GTT TTG CAC GTT CAC CG-3’ (reverse primer), generating a product of 550 bp. The recombined Sptlc1 knock-out allele was identified by PCR using 5’-CAG AGC TAA TGG AAA GGT GTC-3’ (forward primer) and 5’-CTG TTA CTT CTT GCC AGT GGA C-3’ (reverse primer), generating a product of 315 bp. To induce the deletion of Sptlc1 in Figures 1, 3—5, Figure 6A-C, Figure 7, Figure 8, 6- to 12-week-old mice were given 2 mg tamoxifen (Sigma) dissolved in corn oil (Sigma) via intraperitoneal injection for 3 consecutive days. Experiments in the study were performed on animals at least 4 weeks post tamoxifen treatment other than animals used in Figure 6A and B. For Figure 2 to Figure 4B-G and Figure 6D-J, neonates from Sptlc1ECKO strain were given 50 μg tamoxifen via intraperitoneal injection for 3 consecutive days from P1 to P3. Both male and female animals were used for the experiments. All animal experiments were approved by the Boston Children’s Hospital Institutional Animal Care and Use Committee (IACUC).

Cell line

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Human umbilical vein endothelial cells (HUVEC) were purchased from Lonza and cultured in M199 medium (Corning) supplemented with 10% FBS, penicillin–streptomycin, endothelial cell growth factor from sheep brain extract, and 5 U/ml heparin on gelatin–coated dishes in a 37 °C incubator with 5% CO2. Passage 4 – passage 7 cells were used for experiments. Endothelial markers including VE-Cad, CD31, and ERG were used for cell characterization by immunofluorescence.

Detailed cell authentication information of HUVEC can be acquired from Lonza. In brief, routine characterization of HUVEC includes morphological observation throughout serial passages and all lots produced after 01 May 2010 stain at least 90% double-positive for endothelial cell markers CD31/CD105 and negative for alpha smooth muscle actin marker at passage 4. Pre-screened HUVEC are guaranteed to test positive for angiogenesis and vascular cell health markers, eNOS, Tie-2, VEGFr2, and Axl in the first passage out of cryopreservation (From Lonza).

Upon purchase, all cells are performance assayed and test negative for HIV-1, mycoplasma, hepatitis-B, hepatitis-C, bacteria, yeast and fungi. Cell performance and characterization are measured after recovery from cryopreservation.

Mouse EC isolation

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Mouse lung EC were isolated from three to four pairs of lungs dissected from control or Sptlc1 ECKO adult mice 4 weeks post tamoxifen treatment. Freshly isolated lung tissues were minced with scissors and allowed to digest at 37 °C in Liberase (0.6 U/mL, Sigma) in HBSS for 45 min. Samples were further subjected to mechanical disruption by gentleMACS Octo Dissociator (Miltenyi Biotec) and filtration through fine steel mesh (40 µm, Falcon). Cells were washed twice with HBSS containing 0.5% Fatty Acid Free BSA. RBC were removed by ACK lysis buffer (Thermo Fisher). Cells were incubated with CD45 micro beads (Miltenyi Biotec) at 4 °C for 15 min to deplete CD45+ cells. Remaining cells were incubated with CD31 micro beads (Miltenyi Biotec) at 4 °C for 15 min to enrich EC. The purity of each population was determined by flow cytometry.

Cells were stained with stained with phycoerythrin (PE)-conjugated anti-mouse CD31 (BioLegend, 1:200), allophycocyanin (APC)-conjugated anti-mouse CD45 (BioLegend, 1:200) in blocking solution (0.25% FAF-BSA in HBSS) with anti-CD16/32 (BioLegend, 1:200) for 15 min on ice. Stained cells were washed with HBSS containing 10% serum twice and analyzed by BD FACSCalibur Flow Cytometer (BD Biosciences). CD31 and CD45 were gated as shown in Figure 1B.

Western blotting

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Isolated cells from EC isolation procedure and HUVEC were extracted with lysis buffer (50 mM, Tris·HCl (pH 7.4), 0.1 mM EDTA, 0.1 mM EGTA, 1% Nonidet P-40, 0.1% sodium deoxycholate, 0.1% SDS, 100 mM NaCl, 10 mM NaF, 1 mM sodium pyrophosphate, 1 mM sodium orthovanadate, 25 mM sodium β-glycerophosphate, 1 mM Pefabloc SC, and 2 mg/mL protease inhibitor mixture (Roche Diagnostics)). Protein concentration was determined by Dc Protein Assay kit (Bio-Rad). 20 to 50 µg of total proteins were analyzed by SDS/PAGE and transferred onto a nitrocellulose membrane. Blots were blocked with 5% non-fat milk in TBS. Blocked blots were incubated with primary antibodies including SPTLC1 (Santa Cruz, 1:1000), eNOS (BD Biosystem, 1:1000), β-actin (Sigma, 1:5000), phospho-eNOS (Cell Signaling Technology, 1:1000), phospho-ERK (Cell Signaling Technology, 1:2000), ERK (Cell Signaling Technology, 1:2000) at 4 °C overnight. Blots were washed three times with TBSt for 5 min before adding the HRP-conjugated secondary antibody (Millipore, 1:5000). After another three times wash with TBSt, blots were developed with ECL western blotting substrate (Thermo Fisher) and imaged by Azure 600 imaging system (Azure Biosystems).

SL measurement of isolated cells

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Isolated cells from EC isolation procedure were counted and 2–5x106 cells were subjected to HPLC- mass spectrometry (MS/MS) by the Lipidomics Core at the Stony Brook University Lipidomic Core (Stony Brook, NY) using TSQ 7000 triple quadrupole mass spectrometer, operating in a multiple reaction monitoring-positive ionization mode as described (Bielawski et al., 2010).

Retina immunohistochemistry in flat mounts

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Eyeballs from Ctrl and Sptlc1 ECKO mice were enucleated and fixed in 4% Paraformaldehyde (PFA) in PBS at room temperature for 20 min. Retinas were isolated under dissection microscopy, permeabilized in 0.5% Triton X-100 in PBS (PBSt) at room temperature for 30 min and blocked with 1% Bovine Serum Albumin (BSA) in PBSt at room temperature for 30 min. Primary antibodies were added to the sections with indicated dilution in PBSt (NG2 (Sigma, 1:200), Phsopho-histone H3 (BioLegend, 1:200), ESM1 (R and D system, 1:200), LEF1 (Cell Signaling Technology, 1:200), TFRC (Novus Biologicals, 1:200), CLDN5 (Invitrogen, 1:200), MFSD2A (A kind gift from David Silver, 1:200), Alexa Fluor 647 isolectin GS-IB4 conjugate (Invitrogen, 1:500), Alexa Fluor 488-conjugated rabbit monoclonal anti- ERG (Abcam, 1:200), Alexa Fluor 647-conjugated rabbit monoclonal anti- ERG (Abcam, 1:200), Cy3-conjugated mouse monoclonal anti-α-smooth muscle actin (Sigma, 1:500)) at 4 °C overnight. Retinas were further washed three times with PBS for 10 min at room temperature and incubated with fluorescent conjugated secondary antibodies with 1:500 dilution in PBSt for 2 hr at room temperature. Stained retinas were washed three times with PBS for 10 min at room temperature and mounted using Fluoromount-G slide mounting medium (Southern Biotech). Flat Mount Retina Slides were proceeded to image with confocal microscopy (Zeiss).

Oxygen induced retinopathy

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Retinal neovascularization was observed using the OIR model as published (Smith et al., 1994). In brief, neonates together with their mother were exposed to 75% oxygen from P7 to P12. Upon returning to room air (20% O2) at P12 the relative hypoxia induced neovascularization over the period P12 through P17 in these mice, with P17 as the maximum of neovascularization. For experiments in Figure 4H–K, 100 μg tamoxifen was administrated via intraperitoneal injection at P12. Eyeballs were collected at P10, P12 or P17 for immunofluorescence (See section above). Retinal neovascularization and vaso-obliteration were quantified using Image J as previously reported (Stahl et al., 2009).

Intravitreal injection of VEGF-A

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Intravitreal injection of mouse recombinant VEGF-A165 (BioLegend) was performed in P6 pups. Pups were first anesthetized by using crushed ice. Eye lids were carefully separated by 30 G needle and eyeballs were lifted for injection.1 µL of VEGF-A165 at a concentration of 50  ng/μl or 1 µL of saline were injected into the vitreous humor using a Nanofil syringe (World Precision Instrument). Pups were placed onto a heating pad and returned to mom’s care. After 4 hr, eyeballs were collected and processed for retina immunohistochemistry.

SL supplementation to HUVEC

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A total of 100 nM Myriocin (Cayman) were treated to HUVEC for 72 hr in complete M199 medium. They were starved for 24 hr in M199 medium supplemented with 10% charcoal stripped FBS and 4 mg/mL FAF-BSA. 6 hr prior to VEGF treatment, dhSph, Sph and C16:0 Cer (300 nM) were added to the medium. VEGF (50 ng/mL) were then treated for 5 min and protein extracts were harvested in lysis buffer.

Lipid raft staining by Cholera Toxin B

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Lipid rafts were stained by Vybrant Lipid Raft labeling kit (Invitrogen) followed by manufacturer’s instruction.

SL measurement of liver and lung

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Tissues were homogenized in 20 mM Tris-HCl pH 7.5 with tissue homogenizer (Fisher Scientific). Protein concentration was determined by Dc Protein Assay kit (Bio-Rad). Two to 6 mg of total protein were used for HPLC-MS/MS by the Lipidomics Core at the Stony Brook University Lipidomic Core (https://osa.stonybrookmedicine.edu/research-core-facilities/bms Stony Brook, NY) using TSQ 7000 triple quadrupole mass spectrometer, operating in a multiple reaction monitoring-positive ionization mode as described (Bielawski et al., 2010).

S1P measurement in plasma and RBC

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Plasma S1P and RBC S1P in Figure 6A–C was extracted as previously described (Frej et al., 2015) with minor modification. Ten μL of plasma or 5x107 of RBC were first diluted to 100 μL with TBS Buffer (50 mM Tris-HCl pH 7.5, 0.15 M NaCl). S1P was extracted by adding 100 μL precipitation solution (20 nM D7-S1P in methanol) followed by 30 s of vortexing. Precipitated samples were centrifuged at 18,000 rpm for 5 min and supernatant were transferred to vials for UHPLC-MS/MS analysis (see below). C18-S1P (Avanti Lipids) was dissolved in methanol to obtain a 1 mM stock solution. Standard samples were prepared by diluting the stock in 4% fatty acid free BSA (Sigma) in TBS to obtain 1 mM and stored at –80 °C. Before analysis, the 1 mM S1P solution was diluted with 4% BSA in TBS to obtain the following concentrations: 0.5 mM, 0.25 mM, 0.125 mM, 0.0625 mM, 0.03125 mM, 0.0156 mM, and 0.0078 mM. S1P in diluted samples (100 μL) were extracted with 100 μL of methanol containing 20 nM of D7-S1P followed by 30 s of vortexing. Precipitated samples were centrifuged at 18,000 rpm for 5 min and the supernatants were transferred to vials for mass spectrometric analysis. The internal deuterium-labeled standard (D7-S1P, Avanti Lipids) was dissolved in methanol to obtain a 200 nM stock solution and stored at –20 °C. Before analysis, the stock solution was diluted to 20 nM for sample precipitation. The samples were analyzed with Q Exactive mass spectrometer coupled to a Vanquish UHPLC System (Thermo Fisher Scientific). Analytes were separated using a reverse phase column maintained at 60 °C (XSelect CSH C18 XP column 2.5 mm, 2.1 mm X 50 mm, Waters). The gradient solvents were as follows: Solvent A (water/methanol/formic acid 97/2/1 (v/v/v)) and Solvent B (methanol/acetone/water/formic acid 68/29/2/1 (v/v/v/v)). The analytical gradient was run at 0.4 mL/min from 50–100% Solvent B for 5.4 min, 100% for 5.5 min, followed by one minute of 50% Solvent B. A targeted MS2 strategy (also known as parallel reaction monitoring, PRM) was performed to isolate S1P (380.26 m/z) and D7-S1P (387.30 m/z) using a 1.6 m/z window, and the HCD-activated (stepped CE 25, 30,50%) MS2 ions were scanned in the Orbitrap at 70 K. The area under the curve (AUC) of MS2 ions (S1P, 264.2686 m/z; D7-S1P, 271.3125 m/z) was calculated using Skyline (MacLean et al., 2010). Quantitative linearity was determined by plotting the AUC of the standard samples (C18-S1P) normalized by the AUC of internal standard (D7-S1P); (y) versus the spiked concentration of S1P (x). Correlation coefficient (R2) was calculated as the value of the joint variation between x and y. Linear regression equation was used to determined analyte concentrations.

Plasma and RBC collection

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For non-terminal blood collection, blood was collected from submandibular vein via cheek punch. For terminal blood collection, mice were euthanized with CO2. Blood was recovered via vina cava. Blood samples were collected in tubes containing 1–5 μl 0.5 M EDTA depending on sample volume. Samples were centrifuged at 2000 g for 10 min. Plasma samples were collected and stored at –80 °C. RBC were washed twice with HBSS and cell number was counted by hemocytometer. 109 cells were pelleted by centrifugation at 2000 g for 10 min and store at –80 °C for SL measurement.

SL measurement in plasma and retina

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Retinas were placed on dry ice for their extraction. Afterwards, 600 µl of ice cold (Freezer for 1 hr, kept on ice while processing outside) LC-MS methanol was added to each sample, followed by 10 µl of the deuterated sphingolipid labeled internal standards. Samples were then vortexed and allowed to equilibrate on ice for 15 min. This was followed by two 15 min sonication steps in an ice bath. Next, samples were centrifuged at 12,000 g for 15 min at 6°C. Finally, 120 µl of the supernatant were transferred to an LC-MS amber vial equipped with a 150 µl insert for LC-MS injection. A pool of 25 µL of all samples was used as QC of the injection. Samples were injected on an Acquity UPLC system coupled to a Xevo TQ-S mass spectrometer (Waters, Milford, MA) as previously described (Akawi et al., 2021). For plasma analyses, samples were thawed at 4°C in the refrigerator. Then, samples were extracted as previously described (Akawi et al., 2021). Briefly, a volume of 10 µl of the sphingolipid internal standard mix containing labeled internal standards. Samples were then vortexed for 10 s and equilibrated with the internal standard at room temperature. Then, a volume of 250 µl LC-MS methanol was added to each sample, followed by a 10-s vortex period and sonication for 15 min in an ultrasound bath with ice. Next, samples were centrifuged at 12,000 g for 15 min at 6°C. Finally, 120 µl of the supernatant were transferred to an LC-MS amber vial equipped with a 150 µl glass insert. A pool of 25 µL of all samples was used as QC of injection. Samples were then analyzed using the same method as described for the retinas.

APAP-induced liver injury

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Mice were fasted for 16 hr. APAP (Sigma) was dissolved in PBS and administered to the mice via intraperitoneal injection (300 mg/kg). Food and water were given ad lib after treatment. Plasma and liver samples were collected at indicated time for further analysis. Liver function was measured using AST activity assay kits (Sigma) according to the manufacturer’s instructions. Liver GSH levels were measured using glutathione assay kits (Cayman Chemical) according to the manufacturer’s instructions. A lobe of liver was fixed in 4% PFA and processed for paraffin embedding. Sections were stained with hematoxylin and eosin (H & E). Images were captured by Axioskop 2 mot Plus microscope (5 x/0.12).

Confocal microscopy and image processing

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Images were acquired using a LSM810 confocal microscope (Zeiss) equipped with an EC Plan-Neofluar 10 x/0.3, a Plan-Apochromat 20 x/0.8 or a Plan-Apochromat 40 x/1.4 Oil DIC objective. Images were taken using Zen2.1 software (Zeiss) and processed and quantified with Fiji (NIH). Figures were assembled using Affinity Photo and Windows Office Powerpoint.

Quantification of images

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Vascular density quantification (Figure 2B, J and K, Figure 3—figure supplement Figure 3—figure supplements 1 and 2, Figure 4C and F).

Tile-scanned images of flat mounted retinas stained with IB4 were used. IB4+ area was quantified as a percent of area of region of interest via Vessel Analysis plugin on Fiji (NIH). For ‘total vascular density’, z-stack tile-scanned images containing all three plexuses were acquired and used for quantification. For inner plexus density and superficial plexus density, z-stack tile-scanned images containing specified plexus were acquired and used for quantification. IB4+ area was quantified as a percent of total retina area as the vasculature has developed at P10 and P15. Value from a single retina image is shown as a dot.

Vessel outgrowth quantification (Figure 2C).

Tile-scanned images of flat mounted retinas stained with IB4 were used. The distance between the vascular front and the central optic nerve was quantified as a percent of the retinal radius. The mean of values from 4 different leaves of retina is shown as a dot.

Pericyte coverage quantification (Figure 2E).

Tile-scanned images of flat mounted retinas stained with IB4/NG2 were used. NG2+ fraction signal is divided by vascularized area (IB4+). Value from a single retina image is shown as a dot.

Proliferating cell quantification (Figure 2G).

Tile-scanned images of flat mounted retinas stained with IB4/pHH3 and ERG were used. ERG+; pHH3+ cells within the vasculature (IB4+ area) were manually counted. Value from a single retina image is shown as a dot.

Tip cell quantification (Figure 2H).

Tile-scanned images of flat mounted retinas stained with IB4/pHH3 and ERG were used. ERG+; ESM1+ cells were manually counted. Value from a single retina image is shown as a dot.

Positive area of BRB associated gene quantification (Figure 3B, C, E and F).

Tile-scanned images of flat mounted retinas stained with IB4 and either LEF-1, TFRC, MFSD2A and CLDN5 were acquired. The area double-positive for either MFSD2A, TFRC or LEF-1 and IB4 was quantified as a percent of IB4+ area. Value from one representative retinal leave is plotted as a dot.

Vaso-obliteration (VO) area quantification (Figure 4D, G and K).

Tile-scanned images of flat mounted retinas stained with IB4/SMA were used. VO area was determined by avascularized area divided by total retinal area using Affinity Photo software.

Neovascularization (NV) area quantification (Figure 4J).

Tile-scanned images of flat mounted retinas stained with IB4/SMA were used. NV area was determined by manually circling neovascularized area (IB4+/SMA+ areas with abnormal shape than regular vasculature) and divided by total retinal area using Affinity Photo software.

Vascular front EC number quantification (Figure 5B).

Tile-scanned images of flat mounted retinas stained with IB4 and ERG were used. Vascular front areas were manually lassoed based on IB4 signal. Numbers of ERG+ cells were manually counted. Values from a single retina image is shown as a dot.

ESM expressions in capillary plexus quantification (Figure 5C).

Tile-scanned images of flat mounted retinas stained with IB4, ERG and ESM1. Vascular front areas were manually lassoed. Capillary plexus regions were defined as areas outside of vascular front. Numbers of ESM1+/ERG+ cells in both regions were manually counted. Value from a single retina image is shown as a dot.

Necrotic area quantification (Figure 9C).

Necrotic areas were determined manually based on H and E staining and hepatocyte nuclear morphology and further divided by total area of the image. Mean value from 5 representative images is shown as a dot.

Statistics

For datasets containing exactly two groups, an unpaired two-tailed Student’s t test was used to determine significant differences. In Figure 1—figure supplement 1B, Figure 7A and B, one-way ANOVA followed by Bonferroni’s post hoc test was used to determine significant differences at all time points. p Value less than 0.05 was statistically significant.

Appendix 1

Appendix 1—key resources table
Reagent type (species) or resourceDesignationSource or referenceIdentifiersAdditional information
Genetic reagent (M. musculus)Sptlc1fl/fl miceAlexaki et al., 2017 (PMID:28100772)RRID:MMRRC_042294-UCD
Genetic reagent (M. musculus)Cdh5-Cre-ERT2 miceSörensen et al., 2009 (PMID:19144989)RRID:MGI:3848984
Genetic reagent (M. musculus)Sphk1fl/fl micePappu et al., 2007 (PMID:17363629)RRID:MMRRC_030038-UCD
Genetic reagent (M. musculus)Sphk2-/- miceMizugishi et al., 2005 (PMID:16314531)RRID:IMSR_JAX:019140
Genetic reagent (M. musculus)Apom-/- miceChristoffersen et al., 2008 (PMID:18006500)RRID:MGI:3772574
Cell line (Human)Human eubmilical vein endothelial cellsLonzaC2519A
AntibodyAnti-CD31 MicroBeads (rat monoclonal)Miltenyi Biotec130-097-418; RRID:AB_2814657
AntibodyAnti-CD45 MicroBeads (rat monoclonal)Miltenyi Biotec130-052-301; RRID:AB_2877061
Antibody(PE)-conjugated Anti-CD31 (rat monoclonal)Biolegend102508; RRID:AB_312915For EC Isolation (1:250)
Antibody(APC)-conjugated Anti-mouse CD45 (rat monoclonal)Biolegend103112; RRID:AB_312977For EC Isolation (1:250)
AntibodyAnti-SPTLC1 (mouse monoclonal)Santa Cruz Biotechnologysc-374143; RRID:AB_10917035For Western Biotting (1:1000)
AntibodyAnti-phospho eNOS (rabbit monoclonal)Cell Signaling Techonology9571; RRID:AB_329837For Western Biotting (1:1000)
AntibodyAnti-eNOS (rabbit polyclonal)BD BiosciencesCat #:610296; RRID:AB_397691For Western Biotting (1:1000)
AntibodyAnti-β-Actin (mouse monoclonal)Sigma-AldrichCat# A5316; RRID:AB_476743For Western Biotting (1:5000)
AntibodyAnti-rabbit IgG-HRP conjugated (goat polyclonal)AbcamCat# ab205718; RRID:AB_2819160For Western Biotting (1:5000)
AntibodyAnti-mouse IgG-HRP conjugatedMilliporeAP-124P; RRID:AB_9045For Western Biotting (1:5000)
AntibodyAnti-ERK (rabbit polyclonal)Cell Signaling TechonologyCat# 9102; RRID:AB_330744For Western Blotting (1:2000)
AntibodyAnti-phospho ERK (rabbit monoclonal)Cell Signaling TechonologyCat# 9106; RRID:AB_331768For Western Blotting (1:2000)
AntibodyAnti-ApoM (rabbit monoclonal)Abcamab91656; RRID:AB_204916For Western Blotting (1:2000)
AntibodyAnti-NG2 (rabbit polyclonal)Sigma-AldrichAB5320; RRID: AB_91789For Immunofluorescence (1:200)
AntibodyAnti Phospho-histone H3 (Ser28, HTA28) (rat monoclonal)Biolegend641001; RRID: AB_1227660For Immunofluorescence (1:200)
AntibodyAnti-ESM1 (goat polyclonal)R&D SystemsAF1999; RRID: AB_2101810For Immunofluorescence (1:200)
AntibodyAnti-ERG (rabbit monoclonal)AbcamCat# ab92513; RRID:AB_2630401For Immunofluorescence (1:500)
AntibodyAlexa Fluor 488-conjugated Anti- ERG (rabbit monoclonal)Abcamab196374; RRID:AB_2889273For Immunofluorescence (1:200)
AntibodyAlexa Fluor 647-conjugated Anti- ERG (rabbit monoclonal)Abcamab196149For Immunofluorescence (1:200)
AntibodyAnti-LEF1 (rabbit monoclonal)Cell Signaling Techonology2230; RRID:AB_823558For Immunofluorescence (1:200)
AntibodyAnti-TFRC (rat monoclonal)Novus BiologicalsNB100-64979; RRID: AB_962622For Immunofluorescence (1:200)
AntibodyAnti-CLDN5 (rabbit polyclonal)Invitrogen34–1600; RRID: AB_2533157For Immunofluorescence (1:200)
AntibodyAnti-MFSD2A (rabbit polyclonal)Gift from David Silver LabPMID: 23209793For Immunofluorescence (1:200)
AntibodyAnti-Actin, α-Smooth Muscle - Cy3 Antibody (mouse monoclonal)Sigma-AldrichC6198; RRID:AB_476856For Immunofluorescence (1:200)
AntibodyHuman VE-Cadherin Antibody (goat polyclonal)R&D SystemsAF938; RRID:AB_355726For Immunofluorescence (1:200)
Chemical compound or drugTamoxifenSigma-AldrichT5648
Chemical compound or drugCorn OilSigma-AldrichC8267
Chemical compound or drugLiberase TM Research GradeSigma-Aldrich5401127001
Chemical compound or drugACK lysis bufferThermo Fisher ScientificA1049201
Chemical compound or drugAlexa Fluor 647-Conjugated Isolectin GS-IB4 From Griffonia SimplicifoliaThermo Fisher ScientificI32450For Immunofluorescence (1:500)
Chemical compound or drugcOmplete Protease Inhibitor CocktailRoche11836145001
Chemical compound or drugPierce ECL Western Blotting SubstrateThermo Fisher Scientific32106
Chemical compound or drugBovine Serum Albumin lyophilized powder, essentially fatty acid freeSigma-AldrichA6003
Chemical compound or drugFluoromount-G slide mounting mediumSouthernBiotech0100–01
Chemical compound or drugSphingosine-1-Phosphate (d18:1)Avanti Lipids860492 P
Chemical compound or drugsphingosine-1-phosphate-d7Avanti Lipids860659 P-1mg
Chemical compound or drugSphingosine (d18:1)Avanti Lipids860490 P
Chemical compound or drugSphinganine (d18:0)Avanti Lipids860498 P
Chemical compound or drugRecombinant Mouse VEGF-164 (carrier-free)Biolegend583102
Chemical compound or drugAcetaminophenSigma-AldrichA7085
Chemical compound or drugMyriocinCayman Chemical63150
Chemical compound or drugC16 Ceramide (d18:1/16:0)Cayman Chemical10681
Commercial assay or kitDC Protein Assay ReagentsBio-Rad5000116
Commercial assay or kitAST Activity Assay KitSigma-AldrichMAK055
Commercial assay or kitGlutathione Assay KitCayman Chemical703002
Commercial assay or kitVybrant Alexa Fluor 488 Lipid Raft Labeling KitThermo Fisher ScientificV34403
Software, algorithmFijiNIHRRID:SCR_002285
Software, algorithmGraphpad Prism 9.0Graphpad SoftwareRRID:SCR_002798
Software, algorithmAffinity PhotoSerif (Europe)RRID:SCR_016951
Software, algorithmSkylineMacCoss Lab SoftwareRRID: SCR_014080
Sequence-based reagentSptlc1Flox ForAlexaki et al., 2017 (PMID:28100772)RRID:MMRRC_042294-UCDFor genotyping Sptlc1 Flox allele 5’-GGG TTC TAT GGC ACA TTT GGT AAG-3’
Sequence-based reagentSptlc1Flox RevAlexaki et al., 2017 (PMID:28100772)RRID:MMRRC_042294-UCDFor genotyping Sptlc1 Flox allele 5’-CTG TTA CTT CTT GCC AGT GGA C-3’
Sequence-based reagentSptlc1 Flox Deletion ForAlexaki et al., 2017 (PMID:28100772)RRID:MMRRC_042294-UCDFor genotyping Sptlc1 Flox Deletion allele 5’-CAG AGC TAA TGG AAA GGT GTC-3’
Sequence-based reagentSptlc1 Flox Deletion RevAlexaki et al., 2017 (PMID:28100772)RRID:MMRRC_042294-UCDFor genotyping Sptlc1 Flox Deletion allele 5’-CTG TTA CTT CTT GCC AGT GGA C-3’
Sequence-based reagentCdh5-Cre ForSörensen et al., 2009(PMID:19144989)RRID:MGI:3848984For genotyping Cdh5-Cre allele5’-TCC TGA TGG TGC CTA TCC TC-3
Sequence-based reagentCdh5-Cre RevSörensen et al., 2009 (PMID:19144989)RRID:MGI:3848984For genotyping Cdh5-Cre allele 5’-CCT GTT TTG CAC GTT CAC CG-3’
Sequence-based reagentSphk1 Flox Common ForPappu et al., 2007 (PMID:17363629)RRID:MMRRC_030038-UCDFor genotyping Sphk1 Flox allele 5-GGA CCT GGC TAT GGA ACC-3'
Sequence-based reagentSphk1 Flox RevPappu et al., 2007 (PMID:17363629)RRID:MMRRC_030038-UCDFor genotyping Sphk1 Flox allele 5-ATG TTT CTT TCG AGT GAC CC-3'
Sequence-based reagentSphk1Flox Rev DeletionPappu et al., 2007 (PMID:17363629)RRID:MMRRC_030038-UCDFor genotyping Sphk1 Flox Deletion allele 5-AAT GCC TAC TGC TTA CAA TAC-3'
Sequence-based reagentSphk2 Mutant ForMizugishi et al., 2005 (PMID:16314531)RRID:IMSR_JAX:019140For genotyping Sphk2 allele 5'-CTC GTG CTT TAC GGT ATC GC-3'
Sequence-based reagentSphk2 Common RevMizugishi et al., 2005 (PMID:16314531)RRID:IMSR_JAX:019140For genotyping Sphk2 allele 5'-CAC TGC ACC CAG TGT GAA TC-3'
Sequence-based reagentSphk2 Mutant RevMizugishi et al., 2005 (PMID:16314531)RRID:IMSR_JAX:019140For genotyping Sphk2 allele 5'-TCA TCC TGC TGC CCC TTA C-3'
Sequence-based reagentApom For 1Christoffersen et al., 2008 (PMID:18006500)RRID:MGI:3772574For genotyping Apom allele 5'-CAC CCA GCA ACT CAT CCT TT-3'
Sequence-based reagentApom For 2Christoffersen et al., 2008 (PMID:18006500)RRID:MGI:3772574For genotyping Apom allele 5'-GCA GCG CAT CGC CTT CTA TC-3'
Sequence-based reagentApom RevChristoffersen et al., 2008 (PMID:18006500)RRID:MGI:3772574For genotyping Apom allele 5'-TCT TCC CCA CAC CCT AGC TC-3'

Data availability

All data generated or analyzed during this study are included in the manuscript and supporting files. Source data files have been provided for each figure.

References

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    3. Kon J
    4. Tomura H
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    Interaction of sphingosine 1-phosphate with plasma components, including lipoproteins, regulates the lipid receptor-mediated actions
    The Biochemical Journal 352 Pt 3:809–815.
    1. Smith LE
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    6. Sullivan R
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Article and author information

Author details

  1. Andrew Kuo

    Vascular Biology Program, Boston Children’s Hospital, Department of Surgery, Harvard Medical School, Boston, United States
    Contribution
    Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Writing - original draft, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-7263-8658

  2. Antonio Checa

    Unit of Integrative Metabolomics, Institute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden
    Contribution
    Data curation, Formal analysis, Validation, Investigation, Methodology, Writing – review and editing
    Competing interests
    No competing interests declared

  3. Colin Niaudet

    Vascular Biology Program, Boston Children’s Hospital, Department of Surgery, Harvard Medical School, Boston, United States
    Contribution
    Formal analysis, Investigation, Methodology, Writing – review and editing
    Competing interests
    No competing interests declared

  4. Bongnam Jung

    Vascular Biology Program, Boston Children’s Hospital, Department of Surgery, Harvard Medical School, Boston, United States
    Contribution
    Formal analysis, Investigation, Writing – review and editing
    Competing interests
    No competing interests declared

  5. Zhongjie Fu

    Department of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, United States
    Contribution
    Resources, Software, Methodology, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-8182-2983

  6. Craig E Wheelock

    1. Unit of Integrative Metabolomics, Institute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden
    2. Department of Respiratory Medicine and Allergy, Karolinska University Hospital, Stockholm, Sweden
    3. Gunma University Initiative for Advanced Research, Gunma University, Maebashi, Japan
    Contribution
    Resources, Data curation, Formal analysis, Methodology, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-8113-0653

  7. Sasha A Singh

    Center for Interdisciplinary Cardiovascular Sciences, Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, United States
    Contribution
    Resources, Data curation, Methodology, Project administration, Writing – review and editing
    Competing interests
    No competing interests declared

  8. Masanori Aikawa

    Center for Interdisciplinary Cardiovascular Sciences, Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, United States
    Contribution
    Resources, Project administration, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-9275-2079

  9. Lois E Smith

    Department of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, United States
    Contribution
    Resources, Supervision, Methodology, Writing – review and editing
    Competing interests
    Reviewing editor, eLife
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-7644-6410

  10. Richard L Proia

    Genetics and Biochemistry Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, United States
    Contribution
    Conceptualization, Resources, Supervision, Writing – review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-0456-1270

  11. Timothy Hla

    Vascular Biology Program, Boston Children’s Hospital, Department of Surgery, Harvard Medical School, Boston, United States
    Contribution
    Conceptualization, Data curation, Supervision, Funding acquisition, Writing - original draft, Project administration, Writing – review and editing
    For correspondence
    timothy.hla@childrens.harvard.edu
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-8355-4065

Funding

American Heart Association (Postdoctoral Fellowship)

  • Andrew Kuo

National Heart, Lung, and Blood Institute (R35)

  • Timothy Hla

National Eye Institute (R01)

  • Timothy Hla

American Heart Association (18POST33990339)

  • Andrew Kuo

National Heart, Lung, and Blood Institute (HL135821)

  • Timothy Hla

National Eye Institute (EY031715)

  • Timothy Hla

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

We thank Lipidomics Core Facility of Stony Brook University Medical Center for the analytical work in MS. This work was supported in part by the NIH grants (R35-HL135821 and R01EY031715 to TH), Intramural Research Programs of the National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Disease to RLP, National Institutes of Health, and American Heart Association Postdoctoral Fellowship (18POST33990339) to AK.

Ethics

This study was performed in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. All of the animals were handled according to approved institutional animal care and use committee (IACUC) protocols (#19-10-4031R) of the Boston Children's Hospital. Every effort was made to minimize suffering.

Copyright

This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

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  1. Andrew Kuo
  2. Antonio Checa
  3. Colin Niaudet
  4. Bongnam Jung
  5. Zhongjie Fu
  6. Craig E Wheelock
  7. Sasha A Singh
  8. Masanori Aikawa
  9. Lois E Smith
  10. Richard L Proia
  11. Timothy Hla
(2022)
Murine endothelial serine palmitoyltransferase 1 (SPTLC1) is required for vascular development and systemic sphingolipid homeostasis
eLife 11:e78861.
https://doi.org/10.7554/eLife.78861

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https://doi.org/10.7554/eLife.78861

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    Hundreds of myosin 10s are pushed to the tips of filopodia and could cause traffic jams on actin

    Julia Shangguan, Ronald S Rock
    Research Article

    Myosin 10 (Myo10) is a motor protein known for its role in filopodia formation. Although Myo10-driven filopodial dynamics have been characterized, there is no information about the absolute number of Myo10 molecules during the filopodial lifecycle. To better understand molecular stoichiometries and packing restraints in filopodia, we measured Myo10 abundance in these structures. We combined SDS-PAGE densitometry with epifluorescence microscopy to quantitate HaloTag-labeled Myo10 in U2OS cells. About 6% of total intracellular Myo10 localizes to filopodia, where it enriches at opposite cellular ends. Hundreds of Myo10s are in a typical filopodium, and their distribution across filopodia is log-normal. Some filopodial tips even contain more Myo10 than accessible binding sites on the actin filament bundle. Live-cell movies reveal a dense cluster of over a hundred Myo10 molecules that initiates filopodial elongation. Hundreds of Myo10 molecules continue to accumulate during filopodial growth, but accumulation ceases when retraction begins. Rates of filopodial elongation, second-phase elongation, and retraction are inversely related to Myo10 quantities. Our estimates of Myo10 molecules in filopodia provide insight into the physics of packing Myo10, its cargo, and other filopodia-associated proteins in narrow membrane compartments. Our protocol provides a framework for future work analyzing Myo10 abundance and distribution upon perturbation.