Kindlin-2 inhibits TNF/NF-κB-Caspase 8 pathway in hepatocytes to maintain liver development and function
Abstract
Inflammatory liver diseases are a major cause of morbidity and mortality worldwide; however, underlying mechanisms are incompletely understood. Here we show that deleting the focal adhesion protein Kindlin-2 expression in hepatocytes using the Alb-Cre transgenic mice causes a severe inflammation, resulting in premature death. Kindlin-2 loss accelerates hepatocyte apoptosis with subsequent compensatory cell proliferation and accumulation of the collagenous extracellular matrix, leading to massive liver fibrosis and dysfunction. Mechanistically, Kindlin-2 loss abnormally activates the tumor necrosis factor (TNF) pathway. Blocking activation of the TNF signaling pathway by deleting TNF receptor or deletion of Caspase 8 expression in hepatocytes essentially restores liver function and prevents premature death caused by Kindlin-2 loss. Finally, of translational significance, adeno-associated virus mediated overexpression of Kindlin-2 in hepatocytes attenuates the D-galactosamine and lipopolysaccharide-induced liver injury and death in mice. Collectively, we establish that Kindlin-2 acts as a novel intrinsic inhibitor of the TNF pathway to maintain liver homeostasis and may define a useful therapeutic target for liver diseases.
Editor's evaluation
Gao et al. developed various genetic permutations of mouse models of kindlin-2 deficiency in the hepatocytes to decipher its role. Hepatocyte-specific loss of kindlin-2 resulted in severe inflammatory liver injury, accelerated fibrosis/portal hypertension, and massive hepatocyte cell death by apoptosis. These effects are reversed by ablation of TNF signally or by caspase 8 deletion. AAV-mediated replacement of kindlin-2 protects the mice from chemically induced acute liver injury. Together the findings are novel with significant translational potential.
https://doi.org/10.7554/eLife.81792.sa0Introduction
The liver is a multifunctional organ that plays critical roles in regulation of metabolism and detoxification and maintenance of the whole-body homeostasis (Jones et al., 2018). Liver comprised parenchymal cells and non-parenchymal cells. The former includes hepatocytes and endothelial cells; the latter includes hepatic stellate cells (HSC) and Kupffer cells. Abnormal activation of the TNF signaling stimulates inflammation and apoptosis, which are intertwined during the development and progression of liver diseases (Guicciardi and Gores, 2005; Tacke and Zimmermann, 2014; Garcia-Martinez et al., 2016; Schuppan et al., 2018). TNFα exerts its actions through binding and activating two different types of receptors, TNF receptor 1 (TNFR1) and TNFR2 (Wajant and Siegmund, 2019). It is known that NF-κB, a major TNFR downstream effector, plays a pivotal role in promoting inflammatory liver diseases, such as viral and alcoholic hepatitis and fulminant hepatic failure (Ding and Yin, 2004). Thus, it is critical to keep the TNF/NF-κB signaling activity under strict check to maintain normal organogenesis and function. However, key signal(s) that restrict abnormal TNF/TNFR activation in liver under physiological conditions and if and how alterations of these signals contribute to development and progression of inflammatory liver diseases are incompletely understood.
Kindlin proteins are key components of the focal adhesion (FA) assembly and contain the FERM domain, which is responsible for binding to and activating integrins to regulate the cell-extracellular matrix (ECM) adhesion, migration, and signaling (Ma et al., 2008; Montanez et al., 2008; Hirbawi et al., 2017; Sun et al., 2019; Kadry and Calderwood, 2020; Michael and Parsons, 2020). Mammals have three Kindlin proteins, that is, Kindlin-1, Kindlin-2, and Kindlin-3, which are encoded by Fermt1, Fermt2, and Fermt3 genes, respectively. Kindlin-1 and Kindlin-3 are expressed primarily in epithelial and hematopoietic cells, respectively, while Kindlin-2 is widely expressed. Up-regulation of Kindlin-2 expression is implicated in a number of pathological processes, such as tumor formation, progression, and metastasis (Zhan and Zhang, 2018; Sossey-Alaoui et al., 2019). Global deletion of Kindlin-2 expression causes early embryonic lethality at E7.5 in mice (Montanez et al., 2008). Furthermore, Kindlin-2 and other FA-related proteins are widely involved in the control of the development and function of skeleton, kidney, heart, and other organs and tissues (Wu et al., 2015; Zhang et al., 2016; Sun et al., 2017; Gao et al., 2019; Wang et al., 2019b; Zhang et al., 2019; Cao et al., 2020; Fu et al., 2020; He et al., 2020; Lei et al., 2020; Wegermann et al., 2020; Zhu et al., 2020; Eysert et al., 2021; Qin et al., 2021; Wang et al., 2021; Chen et al., 2022; Wu et al., 2022) through both integrin-dependent and integrin-independent mechanisms. We have recently demonstrated that Kindlin-2 haploinsufficiency protects against non-alcoholic fatty liver disease by modulating the transcription factor Foxo1 in hepatocytes (Gao et al., 2022). However, whether and how Kindlin-2 plays a role during liver development is unknown.
In this study, by utilizing biochemical and genetic mouse approaches, we establish that Kindlin-2 acts as a potent inhibitor of the TNF/NF-κB-Caspase 8 pathway in hepatocytes and plays an important role in maintaining normal liver development and function.
Results
Kindlin-2 deletion in hepatocytes causes acute liver injury and premature death in mice
To investigate whether Kindlin-2 plays a role in liver development, we deleted its expression by crossing the floxed Kindlin-2 mice (Fermt2fl/fl) with Alb-Cre transgenic mice. The cross-breeding gave rise to genotypes at the expected Mendelian ratio at birth. Results from quantitative real-time RT-PCR and western blotting analyses revealed that the levels of Fermt2 mRNA and protein were decreased in livers, but not brain, heart, lung, kidney, and spleen, in Fermt2fl/fl; Alb-Cre (KO) mice, compared to those in control littermates (Figure 1—figure supplement 1). Shockingly, all KO mice (>30 mice) died at ages between 4 and 5 weeks (Figure 1a). At 4 weeks of age, both body and liver weights of KO mice were slightly, but significantly, decreased compared to those of control littermates (Figure 1b and c). At this age, livers from KO mice became coarsened and granular (Figure 1d, top panels). Massive ascites was observed in all KO mice but not in control mice (Figure 1d, bottom panels). KO mice displayed a splenomegaly (Figure 1e) and severe cholestasis (Figure 1f). Compared to serum from control mice, serum from KO mice was more yellowish in color (Figure 1g) and displayed elevated serum levels of both direct and indirect bilirubin (Figure 1h), suggesting that the animals suffered from cholestasis. KO mice displayed an osteopenic phenotype with significant reductions in both trabecular and cortical bone volume (Figure 1—figure supplement 2).
We further analyzed serum biochemistry in KO mice and age- and sex-matched littermates. The levels of both serum alanine transaminase (ALT) and aspartate transaminase (AST) activities were increased in KO mice relative to those in control mice, starting as early as 2 weeks of age with most dramatic increases at 4 weeks of age for both enzymes (Figure 1i and j). Furthermore, the levels of serum alkaline phosphatase (Figure 1—figure supplement 3a), γ-glutamyl transferase (Figure 1—figure supplement 3b) and total bile acid (Figure 1—figure supplement 3c) were increased in KO mice relative to those in control mice. The levels of serum protein were reduced in a time-dependent manner (Figure 1k). The level of serum low density lipoprotein was increased and that of serum high density lipoprotein was decreased in KO relative to control mice (Figure 1—figure supplement 3d,e). The levels of serum total cholesterol (TCH) and ammonia were increased in KO versus control mice (Figure 1—figure supplement 3f,g). Results from hematoxylin and eosin (H/E) staining of liver sections of 4-week-old control and KO mice revealed that Kindlin-2 loss caused massive inflammatory cell infiltration in KO liver, especially in areas surrounding the hepatic sinusoidal vessels (Figure 1l). Kindlin-2 loss reduced the glycogen accumulation, as determined by periodic acid-Schiff staining (Figure 1m) and the mRNA expression levels of liver-related genes, including those encoding glutamine synthetase (Gs), apolipoprotein A-I (Apoa), fibrinogen b (Fbn), and transthyretin (Ttr) (Figure 1n–p).
Collectively, these results demonstrate that Kindlin-2 loss in hepatocytes causes a severe liver failure and damages in multiple, resulting in premature death.
Kindlin-2 loss induces dramatic hepatocyte apoptosis and stimulates proliferation of both biliary cells and hepatic stellate cells in liver
A progressive increase in hepatocyte apoptosis was observed in KO mice, as demonstrated by TdT-mediated dUTP nick end labeling (TUNEL) staining (Figure 2a and b and Figure 2—figure supplement 1a). Consistently, immunohistochemical (IHC) staining showed that the immune reactivity of Caspase 3 protein was dramatically increased in KO relative to control livers (Figure 2c). The levels of both active Caspase 3 and p65 protein were increased in KO livers compared to those in control livers in a time-dependent manner (Figure 2—figure supplement 1b and c). Western blotting revealed that level of the pro-apoptotic Bax protein was time dependently increased in KO livers compared to that in control livers (Figure 2d). In contrast, expression of the anti-apoptotic Bcl-2 protein was largely down-regulated in a time-dependent manner by Kindlin-2 deficiency (Figure 2d). Western blotting showed that the levels of the proliferation cell nuclear antigen (Pcna) and cyclin D1 proteins were increased in KO livers compared with those in control livers at 3 and 4 weeks of ages but not at 2 weeks of age (Figure 2e). Results from IHC staining of control and KO liver sections using an anti-Ki67 antibody revealed an increase in cell proliferation in KO liver tissue (Figure 2f and g). Kindlin-2 loss apparently increased the number of cytokeratin 19 (CK19)-expressing cells, that is, the biliary/progenitor cells (Figure 2h). Immunofluorescence (IF) staining revealed that the number of Desmin-expressing cells, that is, HSC was dramatically increased in KO relative to that in control liver tissues (Figure 2i and j).
Kindlin-2 loss stimulates collagen deposition and massive fibrosis in liver
A dramatic increase in collagen deposition was observed in livers of 4-week-old KO mice, as demonstrated by the Masson trichromatic and Sirius red staining (Figure 3a–d). Consistently, results from western blotting revealed that level of α-smooth muscle actin (α-Sma), a marker for fibrosis, was drastically increased in KO livers in a time-dependent manner (Figure 3e). IHC staining was also revealed that α-Sma was upregulated in KO mice (Figure 3f). In addition, the mRNA levels of fibrogenic genes, including those encoding collagen α–1(I) chain (Col1a1), transforming growth factor β1 (Tgfβ1), TIMP metallopeptidase inhibitor 1 (Timp1), actin α2 (Acta2), and collagen type VI, α1 (Col6a1), were up-regulated in KO mice relative to those in control mice (Figure 3g).
Kindlin-2 loss greatly activates the TNF/NF-κB signaling pathway in vitro and in vivo
We further performed RNA-seq analyses from 4-week-old control and KO liver tissues and identified 6746 genes that exhibited statistically significant changes and differential expression (3496 up-regulated genes and 3250 down-regulated genes with log2FC >1.5). Kyoto Encyclopedia of Genes and Genome (KEGG) analysis revealed that Kindlin-2 loss impacted multiple important pathways. Kindlin-2 loss activated TNF signaling pathway, apoptosis, and MAPK pathways in hepatocytes (Figure 4a and b). Consistent with result from the RNA-seq analysis, the serum level of tumor necrosis factor α (Tnfα) was dramatically elevated in 4-week-old KO mice compared to that in control littermates (Figure 4c). Furthermore, the mRNA levels of Tnfα were increased in a time-dependent manner in KO livers compared to those in control livers (Figure 4d). IHC staining of F4/80 revealed massive macrophage infiltration in KO but not control liver tissues (Figure 4e). In addition, the expression of CD19 (B cell marker) and ly6G (neutrophils marker) was increased in KO versus control livers (Figure 4f and g). The numbers of circulating neutrophils, myeloid cells (e.g. monocytes), and blood platelet counts were increased in KO versus control mice (Figure 4h–j and Figure 4—figure supplement 1).
To define the function of Kindlin-2 in hepatocyte in vitro, we knocked down its expression in Huh7 and HepG2 cells. The levels of Fermt2 mRNA and Kindlin-2 protein were dramatically reduced by Fermt2 shRNA (sh-K2) in both Huh7 (Figure 4k and l) and HepG2 cells (Figure 4—figure supplement 2a,b). The mRNA levels of Tnfα and Birc3 (Baculoviral IAP repeat containing 3) were up-regulated by Kindlin-2 knockdown in Huh7 (Figure 4m) and HepG2 cells (Figure 4—figure supplement 2c). ELISA showed a dramatic increase in TNF protein in supernatants of the sh-K2 Huh7 (Figure 4n) and HepG2 cultures (Figure 4—figure supplement 2d). Results from F-actin IF staining showed that Kindlin-2 loss impaired the FA formation and caused a reduced tension (Figure 4o). Moreover, deletion of Kindlin-2 in hepatocyte resulted in defects in cell spreading and attachment (Figure 4p).
Collectively, these results illustrate that ablation of Kindlin-2 in hepatocyte resulted in upregulation of TNF signaling pathway.
TNFR ablation reverses liver lesions and lethality caused by Kindlin-2 deficiency
To determine whether abnormal activation of the TNF signaling plays a key role in mediating the liver damage and death caused by Kindlin-2 deficiency, we globally deleted the expression of the TNF receptors in Kindlin-2 KO mice and determined its effects. We used a breeding strategy by crossing the Tnfr-/- mice, in which both Tnfrsf1a and Tnfrsf1b are globally deleted, with the Alb-Cre; Fermt2fl/+ mice to generate the Tnfr-deficient Kindlin-2 KO mice (referred to as KO/Tnfr-/- hereafter) (Figure 5—figure supplement 1). Tnfr-/- mice were purchased from Shanghai Biomodel Organism Science & Technology Development Co., Ltd. The KO/Tnfr-/- mice were normal at birth with the expected Mendelian ratio. Strikingly, deletion of Tnfr genes completely prevented the premature death of the Kindlin-2 KO mice. In contrast to the fact that all Kindlin-2 KO mice died between 4 and 5 weeks of ages, no KO/Tnfr-/- mice (>30 mice) died during this period of time and beyond (Figure 5a). The levels of serum ALT and AST were significantly lower in KO/Tnfr-/- mice than in Kindlin-2 KO mice (Figure 5b and c). As shown in Figure 5d, deletion of Tnfr genes rescued the liver damage in Kindlin-2 KO mice. The increases in collagen deposition, macrophage infiltration, cell proliferation, fibrosis, and apoptosis caused by Kindlin-2 deficiency were markedly reversed by Tnfr genes deletion (Figure 5e–n).
Caspase 8 deletion in hepatocytes attenuates liver lesions and prevents lethality of Kindlin-2 KO mice
It is known that abnormal inflammation causes cell death, and that Caspase 8 is a major initiator in the death receptor-mediated apoptosis. We therefore next determined whether Kindlin-2 loss causes hepatocyte death and thereby liver lesions and lethality by activating the Caspase 8-dependent apoptotic pathway. To this end, we generated mice lacking both Kindlin-2 and Caspase 8 in hepatocytes (referred to as KO/Casp8-/- hereafter). Shockingly, deletion of Caspase 8 in hepatocytes essentially prevented premature death of Kindlin-2 KO mice (Figure 6a). The levels of serum ALT and AST were significantly lower in KO/Casp8-/- mice than in Kindlin-2 KO mice (Figure 6b and c). Deletion of Caspase 8 restored the liver damage in Kindlin-2 KO mice (Figure 6d). The increases in macrophage infiltration, cell proliferation, fibrosis, and apoptosis caused by Kindlin-2 deficiency were markedly attenuated by Caspase 8 deletion (Figure 6e–l).
AAV8-mediated overexpression of Kindlin-2 in hepatocytes attenuates the GalN/LPS-induced liver injury and death
We finally investigated the effect of Kindlin-2 on the liver injury induced by D-galactosamine (GalN)/lipopolysaccharide (LPS). Immunoblotting analysis detected a dramatic decrease in Kindlin-2 accumulation in the liver tissues of C57BL/6 after administration with GalN/LPS (Figure 7a and b). Next, 8-week-old C57BL/6 mice were first injected via tail vein with adeno-associated virus 8 (AAV8) (2×1011 particles/mouse) expressing Kindlin-2 (AAV8-K2) or (Green fluorescent protein) GFP (AAV8-GFP). After 21 days, mice were treated with GaIN/LPS for 5 hr or a longer period of time (for survival curve experiment) (Figure 7c). The level of Kindlin-2 protein was markedly increased in livers of mice injected with AAV8-K2 (Figure 7d and e). As expected, GalN/LPS resulted in acute death of all mice around 14–15 hr of the treatment. Kindlin-2 overexpression (OE) significantly extended the life span of mice compared with control mice injected with AAV8-GFP (Figure 7f). Kindlin-2 OE improved the gross liver appearance in GalN/LPS-treated mice (Figure 7g). Kindlin-2 OE significantly decreased the levels of serum ALT and AST in GalN/LPS-treated mice (Figure 7h and i), but no difference in untreated Kindlin-2 OE and control mice (Figure 7—figure supplement 1). Results from H/E staining revealed that histological damages in liver caused by GalN/LPS were markedly ameliorated by Kindlin-2 OE (Figure 7j). Furthermore, Kindlin-2 OE decreased GalN/LPS-induced hepatocyte apoptosis, as measured by IHC staining of Caspase-3 and TUNEL staining of liver sections (Figure 7k–m).
Discussion
In this study, we demonstrate a novel role of the key FA protein Kindlin-2 in regulation of liver development and function. Kindlin-2 loss in hepatocytes causes an acute liver failure and premature death in mice. We demonstrate that Kindlin-2 loss dramatically activates the TNF/NF-κB signaling pathway, massive inflammation, and hepatocyte death with subsequent stimulation of proliferation of both biliary cells and HSCs, leading to ECM accumulation and fibrosis in liver. We further demonstrate that liver damages and lethality caused by Kindlin-2 deficiency are largely attenuated or completely rescued by either global ablation of TNFR or hepatocyte-selective deletion of Caspase 8 expression. We finally demonstrate that adeno-associated virus mediated OE of Kindlin-2 in hepatocytes attenuates the GalN/LPS-induced liver injury and death in mice.
In this study, we demonstrate that Kindlin-2 expression in hepatocytes is essential for liver development and function. Kindlin-2 deletion in hepatocytes using the Alb-Cre transgenic mice causes acute liver failure and lethality of 100% penetration in mice at ages between 4 and 5 weeks. Our results suggest that abnormal activation of the TNF/NF-κB signaling pathway plays a major role in mediation of the liver lesions and lethality caused by Kindlin-2 deficiency. This notion is supported by the following lines of in vitro and in vivo evidence. First, results from our RNA-seq analyses from 4-week-old control and KO liver tissues reveal that TNF signaling pathway is activated in KO liver. Second, the levels of Tnfα mRNA in liver and serum level of TNFα protein were dramatically elevated in 4-week-old KO versus control mice. Consistently, massive macrophage infiltration is observed in KO but not control liver tissues, suggesting increased inflammation. Third, in vitro studies show that shRNA knockdown of Fermt2 expression increases the mRNA levels of Tnfα and Birc3 in Huh7 and HepG2 cells. Fourth, the increases in serum ALT and AST, hepatocyte apoptosis, ECM deposition, inflammatory infiltration, proliferation of both biliary cells and HSCs, and liver fibrosis caused by Kindlin-2 deficiency were largely reversed by Tnfr genes deletion. Most importantly, Tnfr genes deletion completely rescues the lethality caused by Kindlin-2 deficiency. These findings also indicate the necessity to keep the TNF/NF-κB signaling pathway in hepatocytes under precise control in order to maintain normal liver development and function as well as the whole-body metabolic homeostasis. We demonstrate that Kindlin-2 plays a pivotal role in this regard.
Kindlin-2 loss induces massive hepatocyte apoptosis. The expression of the pro-apoptotic Bax protein is up-regulated and that of the anti-apoptotic Bcl2 protein is down-regulated in mutant liver. A number of apoptotic hepatocytes are observed throughout the mutant liver. Strikingly, genetic ablation of Caspase 8 expression in hepatocytes essentially rescues the liver lesions and lethality caused by Kindlin-2 loss. These results suggest that the Caspase 8-dependent death receptor-mediated apoptotic pathway plays a critical role in mediating the liver damages and lethality caused by Kindlin-2 loss. Abnormal inflammation induced by Kindlin-2 loss should largely contribute to hepatocyte apoptosis in the mutant mice.
Notably, Kindlin-2 loss greatly promotes proliferation of both biliary cells and HSCs and stimulates accumulation and deposition of excessive collagenous ECM, which leads to liver fibrosis in the mutant mice.
It should be noted that KO mice display a splenomegaly and severe cholestasis. These results along with the severe fibrosis strongly suggest the presence of portal hypertension in the mutant mice. It should also be noted that Kindlin-2 loss causes a significant reduction in bone mass. This could be in part due to the dyslipidemia induced by liver dysfunction, which is known to induce hepatic osteodystrophy (Zaidi et al., 2022).
Of translational significance, AAV8-mediated expression of Kindlin-2 in liver significantly blocks the D-GalN/LPS-induced liver inflammation and death in mice. In the future, it would be important to investigate whether Kindlin-2 loss plays a role in the pathogenesis of human inflammatory liver diseases.
In summary, we establish that the FA protein Kindlin-2 is a potent intrinsic inhibitor of the TNF/NF-κB-Caspase 8 inflammatory pathway and plays an important role in the maintenance of normal liver development and function. We may define a novel therapeutic target for inflammatory liver diseases.
Materials and methods
Animal study
Request a detailed protocolGeneration of Fermt2fl/fl mice was previously described (Gao et al., 2019). To delete Kindlin-2 expression in hepatocyte, we first bred the Fermt2fl/fl mice with the Alb-Cre transgenic mice (Wang et al., 2019a), which were kindly provided by Dr. Yan Li of Southern University of Science and Technology, and obtained the Fermt2fl/+; Alb-Cre mice. Further intercrossing of the Fermt2fl/+; Alb-Cre mice with Fermt2fl/fl mice generated the Fermt2fl/fl; Alb-Cre mice, the hepatocyte conditional Kindlin-2 knockout mice (referred to as KO). The Cre-negative floxed Kindlin-2 mice (Fermt2fl/fl) were used as controls in this study. Tnfrsf1a-/- and Tnfrsf1b-/- mice were obtained from the Shanghai Model Organism. Caspase 8fl/fl (Casp8) mice were used as indicated (Gao et al., 2021). All mice used in this study have been crossed with normal C57BL/6 mice for more than 10 generations. Mice were maintained in 12 hr light/dark cycles, with unrestricted access to food and water. All animal experiments were approved and conducted in the specific pathogen free Experimental Animal Center of Southern University of Science and Technology (Approval number: 20200074).
Biochemical measurements
Request a detailed protocolBlood and tissues were collected from mice under anesthesia with isoflurane. Blood collected was allowed to clot for 2 hr at room temperature and then centrifuged to collect serum. TCH, AST, ALT, and albumin were measured with commercial kits (Shensuoyoufu, Shanghai, China).
Histological analyses
Request a detailed protocolTissues were fixed in 4% PFA and then embedded in paraffin. Serial 5 μm paraffin sections were used for H/E staining using our standard protocols. Masson trichrome staining and Sirius Red staining were performed as described previously (Ni et al., 2014). Immunohistochemistry was performed using paraffin sections according to a protocol previously described (Cao et al., 2020). In brief, samples were deparaffinized and rehydrated, followed by antigen retrieval in 10 mM sodium citrate. Blocking and staining were performed in antibody diluent with background-reducing components (DAKO). Samples were incubated with primary antibodies as listed in Supplementary file 1, followed by appropriate secondary antibodies. Images were obtained using a light microscope equipped with a digital camera.
Immunofluorescence staining
Request a detailed protocolIF staining was performed as previously described (Cao et al., 2020). Briefly, liver frozen sections (10 μm thickness) were prepared using a Leica cryostat, fixed in 4% paraformaldehyde for 30 min, blocked for 2 hr with 5% normal goat serum supplemented with 1% BSA, and incubated with the indicated antibodies at 4°C overnight. The sections were incubated with appropriate fluorescence-labeled secondary antibodies and analyzed by IF microscopy.
Cell culture in vitro
Request a detailed protocolHepG2 (cat# SCSP-510) and Huh7 (cat# TCHu182) cells were purchased from the Cell Bank of the Chinese Academy of Sciences and cultured in DMEM supplemented with 10% fetal bovine serum, 1% penicillin, and streptomycin in a 5% CO2 incubator at 37°C. All cell lines tested negative for mycoplasma contamination.
Western blot analysis
Request a detailed protocolFor western blotting, total protein samples were extracted from tissues or cells, and 30 μg of protein samples were separated on a 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis gel and transferred to a polyvinylidene fluoride membrane. Protein expression was visualized by incubating primary antibodies overnight at 4°C, followed by the corresponding secondary antibodies, and developed using the enhanced chemiluminescence system (Bio-Rad, #1705040) (Gao et al., 2012; Gao et al., 2021). Antibodies information is described in Supplementary file 1a.
RNA-seq data and GO/KEGG enrichment analyses
Request a detailed protocolTotal RNAs were extracted from livers of 4-week-old control and KO mice. The sequencing library was determined by an Agilent 2100 Bioanalyzer using the Agilent DNA 1000 Chip Kit (Agilent, #5067–1504). Differentially expressed genes (DEGs) were selected with p-value <0.05, log2FC >1 or < −1, and FPKM >5 in at least one condition. Volcano plot showing dysregulated genes between control and KO livers was generated using R programming. GO and KEGG enrichment analyses were performed on the DEGs using TBtools.
Quantitative real-time RT-PCR analysis
Request a detailed protocolTotal RNA from tissues and cells was extracted with Trizol reagent (Invitrogen, #10296010) as described (Gao et al., 2017). After total RNA isolation and cDNA synthesis, PCR amplification was performed with the SYBR Green PCR Master Mix (Bio-Rad, #1725200). The mRNA expression levels of the target genes were normalized to expression of the glyceraldehyde 3-phosphate dehydrogenase (Gapdh). Each sample was tested at least in triplicate and repeated using three independent cell preparations. Primer sequences are listed in the Supplementary file 1b and Supplementary file 1c.
TUNEL assay
Request a detailed protocolLiver frozen sections were fixed with 4% paraformaldehyde and subjected to TUNEL staining using an In Situ Cell Death Detection Kit (Beyotime Biotechnology, #C1089), following manufacturer’s procedure.
Enzyme-linked immunosorbent assay (ELISA)
Request a detailed protocolAfter collection of serum from mice and supernatants from cultured hepatocytes, TNFα (R&D System, #MTA00B and DTA00D) and Il1β (R&D System, #MLB00C) levels were measured by ELISA kit according to manufacturer’s instruction.
Statistical analysis
Request a detailed protocolThe sample size in mouse experiments of this study was determined based on our previous experience. Mice were randomly grouped in experiments in this study. IF, IHC, and histology were performed and analyzed in a double-blinded way. The two-tailed unpaired Student’s t test (two groups) and one-way ANOVA (multiple groups), followed by Tukey’s post-hoc test, were used for statistical analyses using Prism GraphPad. The results are presented as means ± SEM (standard error of mean). p<0.05 was considered statistically significant.
Data availability
All data generated or analysed during this study are included in the manuscript and supporting file; Source Data files have been provided for Figures 1-7 and figure supplements.
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Article and author information
Author details
Funding
National Key Research and Development Program of China (2019YFA0906004)
- Guozhi Xiao
National Natural Science Foundation of China (82230081)
- Guozhi Xiao
Shenzhen Municipal Science and Technology Innovation Council (JCYJ20180302174246105)
- Huanqing Gao
Shenzhen Municipal Science and Technology Innovation Council (JCYJ20220818100617036)
- Guozhi Xiao
Guangdong Provincial Science and Technology Innovation Council Grant (2017B030301018)
- Guozhi Xiao
Shenzhen Municipal Science and Technology Innovation Council (ZDSYS20140509142721429)
- Guozhi Xiao
National Natural Science Foundation of China (82250710175)
- Guozhi Xiao
National Natural Science Foundation of China (82172375)
- Guozhi Xiao
National Natural Science Foundation of China (81991513)
- Guozhi Xiao
National Natural Science Foundation of China (81870532)
- Guozhi Xiao
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Acknowledgements
The authors acknowledge the assistance of Core Research Facilities of SUSTech. This work was in part supported by the National Key Research and Development Program of China Grants (2019YFA0906004), the National Natural Science Foundation of China Grants (82230081, 82250710175, 82172375, 81991513 and 81870532), the Shenzhen Municipal Science and Technology Innovation Council Grants (JCYJ20220818100617036, JCYJ20180302174246105 and ZDSYS20140509142721429) and the Guangdong Provincial Science and Technology Innovation Council Grant (2017B030301018).
Ethics
All animal experiments were approved and conducted in the specific pathogen free (SPF) Experimental Animal Center of Southern University of Science and Technology (Approval number: 20200074).
Copyright
© 2023, Gao, Zhong, Zhou et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
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Further reading
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- Cell Biology
Aggregation of mutant forms of Huntingtin is the underlying feature of neurodegeneration observed in Huntington's disorder. In addition to neurons, cellular processes in non-neuronal cell types are also shown to be affected. Cells expressing neurodegeneration-associated mutant proteins show altered uptake of ligands, suggestive of impaired endocytosis, in a manner as yet unknown. Using live cell imaging, we show that clathrin-mediated endocytosis (CME) is affected in Drosophila hemocytes and mammalian cells containing Huntingtin aggregates. This is also accompanied by alterations in the organization of the actin cytoskeleton resulting in increased cellular stiffness. Further, we find that Huntingtin aggregates sequester actin and actin-modifying proteins. Overexpression of Hip1 or Arp3 (actin-interacting proteins) could restore CME and cellular stiffness in cells containing Huntingtin aggregates. Neurodegeneration driven by pathogenic Huntingtin was also rescued upon overexpression of either Hip1 or Arp3 in Drosophila. Examination of other pathogenic aggregates revealed that TDP-43 also displayed defective CME, altered actin organization and increased stiffness, similar to pathogenic Huntingtin. Together, our results point to an intimate connection between dysfunctional CME, actin misorganization and increased cellular stiffness caused by alteration in the local intracellular environment by pathogenic aggregates.
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- Cell Biology
- Developmental Biology
The bone-resorbing activity of osteoclasts plays a critical role in the life-long remodeling of our bones that is perturbed in many bone loss diseases. Multinucleated osteoclasts are formed by the fusion of precursor cells, and larger cells – generated by an increased number of cell fusion events – have higher resorptive activity. We find that osteoclast fusion and bone resorption are promoted by reactive oxygen species (ROS) signaling and by an unconventional low molecular weight species of La protein, located at the osteoclast surface. Here, we develop the hypothesis that La’s unique regulatory role in osteoclast multinucleation and function is controlled by an ROS switch in La trafficking. Using antibodies that recognize reduced or oxidized species of La, we find that differentiating osteoclasts enrich an oxidized species of La at the cell surface, which is distinct from the reduced La species conventionally localized within cell nuclei. ROS signaling triggers the shift from reduced to oxidized La species, its dephosphorylation and delivery to the surface of osteoclasts, where La promotes multinucleation and resorptive activity. Moreover, intracellular ROS signaling in differentiating osteoclasts oxidizes critical cysteine residues in the C-terminal half of La, producing this unconventional La species that promotes osteoclast fusion. Our findings suggest that redox signaling induces changes in the location and function of La and may represent a promising target for novel skeletal therapies.