Abstract
β-carotene oxygenase 1 (BCO1) catalyzes the cleavage of β-carotene to form vitamin A. Besides its role in vision, vitamin A regulates the expression of genes involved in lipid metabolism and immune cell differentiation. BCO1 activity is associated with the reduction of plasma cholesterol in humans and mice, while dietary β-carotene reduces hepatic lipid secretion and delays atherosclerosis progression in various experimental models. Here we show that β-carotene also accelerates atherosclerosis resolution in two independent murine models, independently of changes in body weight gain or plasma lipid profile. Experiments in Bco1-/- mice implicate vitamin A production in the effects of β-carotene on atherosclerosis resolution. To explore the direct implication of dietary β-carotene on regulatory T cells (Tregs) differentiation, we utilized anti-CD25 monoclonal antibody infusions. Our data show that β-carotene favors Treg expansion in the plaque, and that the partial inhibition of Tregs mitigates the effect of β-carotene on atherosclerosis resolution. Our data highlight the potential of β-carotene and BCO1 activity in the resolution of atherosclerotic cardiovascular disease.
1. Introduction
Atherosclerotic cardiovascular disease is a progressive pathological process initiated by the accumulation of cholesterol-rich lipoproteins within the intima layer of the arterial wall. These particles ultimately lead to the production of chemoattractant cues for circulating monocytes that transmigrate across the endothelial layer to reach the intima and then differentiate to macrophages to become cholesterol-laden foam cells. During lesion development, macrophages promote local inflammation and plaque weakening by degrading extracellular matrix components such as collagen fibers, which can evolve in the rupture of the lesion and thrombus formation [1].
Conventional therapies aim to lower plasma cholesterol to mitigate the progression of atherosclerosis. Novel strategies are currently under development to stimulate the resolution of plaque inflammation more directly, and eventually a reduction in lesion size, in a process named atherosclerosis regression [2]. Among these strategies, the modulation of CD4+ regulatory T cells (Tregs) number is gaining interest over the past years since the discovery that regressing lesions are enriched in Tregs, where they promote plaque stabilization and repair [3, 4]. Tregs typically express the surface marker CD25, which has been utilized to target and eliminate Tregs [5, 6]. However, strategies to deplete CD25+ Tregs do not affect CD25- Tregs, which possess similar immunomodulatory properties as CD25+ Tregs [7]. Among the different Tregs markers, the forkhead box P3 (FoxP3) acts as lineage specification factor regulating gene expression of proteins implicated in the immunosuppressive activity of these cells [8]. Cell culture studies show that retinoic acid, the transcriptionally active form of vitamin A, promotes Treg differentiation by upregulating FoxP3 expression [9], however, whether dietary vitamin A affects Tregs during atherosclerosis development and resolution remains unanswered.
Humans obtain vitamin A primarily from β-carotene and other provitamin A carotenoids present in most fruits and vegetables. Upon absorption, provitamin A carotenoids are cleaved by the action of β-carotene oxygenase 1 (BCO1), the limiting enzyme in vitamin A formation [10]. Our data show that the enzymatic activity of BCO1 mediates the bioactive actions of β-carotene in various preclinical models of obesity and atherosclerosis [11–16]. We showed that the dietary supplementation with β-carotene delays atherosclerosis progression by reducing cholesterol hepatic secretion in low-density lipoprotein receptor (LDLR)-deficient (Ldlr-/-) mice [15]. We also reported that subjects harboring a genetic variant linked to greater BCO1 activity was associated with a reduction in plasma cholesterol [17].
In this study, we tested the effect of dietary β-carotene on atherosclerosis resolution in two independent experimental models. We characterized plaque composition by probing for macrophage and collagen contents, two parameters utilized to characterize atherosclerotic lesions undergoing resolution [18–21]. Lastly, we utilized Bco1-/- mice and CD25+ Treg depletion experiments in Foxp3EGFP mice to tease out the direct implications of vitamin A formation and Tregs on atherosclerosis resolution.
2. Methods
2.1. Animal husbandry and diets
All procedures were approved by the Institutional Animal Care and Use Committees of the University of Illinois at Urbana Champaign. For all our studies, we utilized comparable number of male and female wild-type, Ldlr-/- (#002207, Jackson Labs, Bar Harbor, ME), Bco1-/- [11], and Foxp3EGFP mice (#006772, Jackson Labs). All mice were in C57BL/6J background. Mice were kept under controlled temperature and humidity conditions with a 12-hours light/dark cycle and free access to food and water. Mice were weaned at three weeks of age onto a breeder diet (Teklad global 18% protein diet: Envigo, Indianapolis, IN) in groups of three to four mice. Control and β-carotene diets contained either placebo beadlets or β-carotene beadlets at a final concentration of 50 mg β-carotene/kg diet. For reference, the content of β-carotene in carroys is 80 mg/kg (USDA Database). Beadlets were a generous gift from DSM Nutritional Products (Sisseln, Switzerland). All diets were prepared by Research Diets (New Brunswick, NJ) by cold extrusion. The exact composition of all the diets used for this study are provided in Supplementary Table 1. For all the experiments, we stimulated the development of atherosclerosis with a Western diet deficient in vitamin A (WD-VAD), as done in the past [15, 17].
2.2. Blood sampling and tissue collection
Before tissue harvesting, mice were deeply anesthetized by intraperitoneal injection with a mixture of ketamine and xylazine at 80 and 8 mg/kg body weight, respectively. We collected blood by cardiac puncture using ethylenediaminetetraacetic acid (EDTA)-coated syringes. We then perfused the mice with 10% sucrose in 0.9% sodium chloride (NaCl)-saline solution prior to tissue harvesting. Tissues were immediately snap-frozen in liquid nitrogen and kept at -80 °C. Aortic roots were collected after removing fat under a binocular microscope, embedded in optimum cutting temperature compound (OCT, Tissue-Tek, Sakura, Torrance, CA) and kept at – 80°C.
2.3. Antisense oligonucleotide (ASO) targeting LDLR expression (ASO-LDLR)
To transiently deplete LDLR expression in wild-type, Bco1-/-, and Foxp3EGFP mice, we administered weekly an intraperitoneal injection containing 5 mg/kg body weight of ASO-LDLR for a period of 16 weeks. At the end of the treatment, we injected a single dose of 20 mg/kg of the sense oligonucleotide (SO-LDLR) antidote, which binds and deactivates the ASO-LDLR [22]. All oligonucleotide treatments were generously provided by Ionis Pharmaceuticals (Carlsbad, CA).
2.4. HPLC analyses of carotenoids and retinoids
Nonpolar compounds were extracted from 100 μl of plasma or 30 mg of liver under a dim yellow safety light using methanol, acetone, and hexanes. The extracted organic layers were then pooled and dried in a SpeedVac (Eppendorf, Hamburg, Germany). We performed the HPLC with a normal phase Zobax Sil (5 μm, 4.6 × 150 mm) column (Agilent, Santa Clara, CA). Isocratic chromatographic separation was achieved with 10% ethyl acetate/hexane at a flow rate of 1.4 ml/min. For molar quantification of β-carotene and retinoids, we scaled the HPLC with a standard curve using the parent compound.
2.5. Plasma lipid analyses
We measured plasma total cholesterol, cholesterol in the high-density lipoprotein fraction (HDL-C), and triglyceride levels using commercially available kits (FUJIFILM Wako Diagnostic, Mountain View, CA), according to the manufacturer’s instructions.
2.6. RNA isolation and RT-PCR
We isolated the total RNA using TRIzol reagent (Thermo Fisher Scientific, Waltham, MA) and Direct-zol RNA Miniprep kit (Zymo Research, Irvine, CA) according to the manufacturer’s instructions. RNA was reverse-transcribed to cDNA using high-capacity cDNA reverse transcription kit (Applied Biosystems, Foster City, CA). Then we used Taqman Master Mix (Applied Biosystems) to perform RT-PCR using the StepOnePlus RT-PCR system (ABI 7700, Applied Biosystems). We calculated the relative gene expression using the ΔCt method and normalized the data to β-actin (Actb). Probes (Applied Biosystems) include mouse Ldlr (Mm00440169_m1), mouse cytochrome P450 26a1 (Cyp26a1, Mm00514486_m1) and mouse Actb (Mm02619580_g1).
2.7. Western blot analysis
For the determination of hepatic levels of LDLR, proteins were extracted from liver lysates in RIPA buffer (50 mM Tris pH 7.4, 150 mM NaCl, 0.25% sodium deoxycholate, 1% Nonidet P-40) in the presence of protease inhibitors. Total protein amounts were quantified using the Pierce® BCA Protein Assay Kit (ThermoFisher Scientific, Waltham, MA). A total of 80 µg of protein homogenate were separated by SDS-PAGE and transferred onto PVDF membranes (Bio-Rad, Hercules, CA). Membranes were blocked with fat-free milk powder (5% w/v) dissolved in Tris-buffered saline (15 mM NaCl and 10 mM Tris/HCl, pH 7.5) containing 0.01% Tween 100 (TBS-T), washed, and incubated overnight at 4 °C with mouse anti-LDLR (Santa Cruz Biotechnologies, Dallas, TX) and mouse anti-GAPDH (ThermoFisher Scientific) as a housekeeping control. Infrared fluorescent-labeled secondary antibodies were prepared at 1:15,000 dilution in TBS-T with 5% fat-free milk powder and incubated for 1 h at room temperature.
2.8. Treg depletion in Foxp3EGFP mice
To deplete Tregs, mice were injected twice with 250 µg of either the isotype control IgG (Ultra-LEAFPurified Rat IgG1, λ Isotype Ctrl Antibody no. 401916, Biolegend, CA) or PC61 anti-CD25 monoclonal antibody (Ultra-LEAF Purified anti-mouse CD25 Antibody no. 102040, Biolegend, CA). The first treatment took place a day after the administration of SO-LDLR, and the second injection two weeks after, following established protocols [6].
2.9. Monocyte/macrophage trafficking studies
One week before harvesting the baseline group, we injected the mice intraperitoneally with 4 mg/ml of 5-ethynyl-2′-deoxyuridine (EdU) (Invitrogen, Waltham, MA) with the goal of labeling circulating monocytes to assess macrophage retention among groups. To compare monocyte recruitment among groups, we labeled circulating monocytes by injecting the mice retro-orbitally with 1 µm diameter Flouresbrite flash red plain microspheres beads (Polysciences Inc, Warrington, PA) diluted in sterile PBS 24 hours before harvesting, regardless of the experimental group. We assessed the efficiency of EdU and bead labeling by flow cytometry 48 hours and 24 hours after injection by tail bleeding, respectively [23].
2.9. Flow cytometry
To assess the number of monocytes labeled with either EdU or fluorescent beads, we incubated blood samples with red blood cell lysis buffer (Thermo Fisher Scientific, Waltham, MA) and blocked unspecific bindings with using anti-mouse CD16/CD32 (Mouse BD Fc Block, BD Biosciences, Franklin Lakes, NJ). Cells were then stained with FITC-conjugated anti-mouse CD45 (BioLegend), PE-conjugated anti-mouse CD115 (BioLegend), and PerCP-conjugated anti-mouse Ly6C/G (BioLegend, San Diego, CA) for 30 minutes on ice. Cells were fixed, permeabilized, and stained for EdU using Click-iT EdU Pacific Blue Flow Cytometry Assay Kit (Invitrogen) following manufacturer’s instructions. Beads were detected with the 640-nm red laser using a 660/20 bandpass filter. Monocyte recruitment and egress was estimated based on monocyte labeling efficiency, following established protocols [24].
For Treg quantifications, spleens were mashed and filtered through a 100 µm sterile cell strainer (Thermo Fisher Scientific). Blood and spleen homogenates were incubated with red blood cell lysis buffer (Thermo Fisher Scientific) and subsequently blocked with anti-mouse CD16/CD32 (BD Biosciences). We stained the cells with Fixable Viability Dye eFluor 780 (eBioscience, San Diego, CA) and eFluor 506-conjugated anti-mouse CD45 (BioLegend), PE-conjugated anti-mouse CD3e (BioLegend), FITC-conjugated anti-mouse CD4 (BioLegend), and BV421-conjugated anti-mouse CD25 (BioLegend) for 30 minutes on ice. We washed the cells twice before fixing and permeabilizing cell membranes using the eBioscience FoxP3/Transcription Factor Staining Buffer Set (Invitrogen) for 1 hour at room temperature, followed by incubation with Alexa Fluor 647-conjugated anti-mouse FoxP3 antibody (BioLegend) for 30 minutes at room temperature. All samples were measured on a BD LSR II analyzer (BD Biosciences) and results were analyzed with the FCS express 5 software (De Novo Software, Pasadena, CA).
2.10. Atherosclerotic lesion analysis
Six μm-thick sections were fixed and permeabilized with ice-cold acetone, blocked, and stained with rat anti-mouse CD68 primary antibody (Bio-Rad, Hercules, CA) followed by biotinylated rabbit anti-rat IgG secondary antibody (Vector Laboratories, Burlingame, CA). CD68+ area was visualized using a Vectastain ABC kit (Vector Laboratories). Sections were then counterstained with hematoxylin, dehydrated in an ethanol gradient, xylene, and mounted with Permount medium (Thermo Fisher Scientific). Images were acquired using Axioskop 40 microscope (Carl Zeiss, Jena, Germany). For collagen content, frozen sections were fixed and stained using picrosirius red (Polysciences). Sections were scanned using the Axioscan.Z1 microscope (Carl Zeiss) using both bright field and polarized light. Total lesion area, CD68+, and collagen+ areas were quantified using ImageJ software (NIH).
2.11. Statistical Analysis
Data represented as bar charts are expressed as mean ± standard error of the mean (SEM). Data were analyzed using GraphPad Prism software (GraphPad Software Inc., San Diego, CA) by one-way ANOVA, followed by Tukey’s multiple comparisons test. Differences between groups were considered significant with an adjusted P value < 0.05. The relationship between the two dependent factors, CD68 and collagen contents, and group differences were evaluated by descriptive discriminant analysis. Briefly, models were fitted under null and alternative hypotheses and goodness of fit was evaluated using the Likelihood Ratio Test with randomized inference (bootstrap; n = 1000 simulations). Simultaneous hypothesis testing was corrected using the Benjamini-Hochberg procedure [24]. The resulting False Discovery Rate (FDR) was considered significant with a cut-off < 0.05.
3. Results
3.1. β-carotene supplementation accelerates atherosclerosis resolution
We recently showed that dietary β-carotene delays atherosclerosis progression in Ldlr-/- mice [15], which prompted us to examine whether β-carotene also impacts the resolution of inflammation in complex atherosclerotic lesions. To achieve these lesions, we utilized two distinct mouse models of atherosclerosis in combination with WD-VAD. In our first model, we established LDLR deficiency in wild-type mice by injecting ASO-LDLR weekly for a period of 16 weeks. The characteristics of the plaques before undergoing resolution were established by sacrificing a subset of mice after 16 weeks on diet (Baseline). The remaining mice were injected once with SO-LDLR to promote atherosclerosis resolution and divided into two groups fed either WD-VAD (Resolution – Control) or WD-β-carotene (Resolution – β-carotene). Mice were harvested three weeks after SO-LDLR injections (Figure 1A).
Male mice gained more weight than female mice, although we did not observe differences between the three experimental groups (Supplementary Figure 1A). For the remaining outcomes (plasma lipid profile, retinoid levels, and plaque composition), we did not observe sex differences in any of our experiments, and therefore, we combined results from both sexes. In comparison to Baseline mice, both Resolution groups showed drastic reduction in total plasma cholesterol and triglyceride levels, while HDL-C levels remained constant between groups (Figure 1B). Lipid normalization was accompanied by the upregulation of hepatic LDLR expression at the mRNA and protein levels (Figure 1C, D).
Despite mice being fed a WD-VAD for several weeks, HPLC measurements of circulating vitamin A and hepatic retinoid stores ruled out vitamin A deficiency in any of the experimental groups (Figure 1E, F). However, mice fed WD-β-carotene showed an increase in hepatic vitamin A content in comparison to those fed WD-VAD, which was mediated by the conversion of β-carotene to vitamin A (Figure 1F). Hepatic Cyp26a1 expression, which is commonly utilized as a surrogate marker of vitamin A and retinoic acid production [25, 26], appeared upregulated in response to WD-β-carotene (Supplementary Figure 1B).
To determine the effect of β-carotene supplementation on atherosclerosis resolution, we examined lesion size and composition at the level of the aortic root (Figure 1G). Lesion area remained constant among the three experimental groups, as previously reported in mice treated with ASO-LDLR under similar experimental conditions (Figure 1H) [27]. We next examined plaque composition by focusing on two parameters commonly utilized as a surrogate indicators of atherosclerosis resolution: CD68+ area, a myeloid (macrophage) marker that represents plaque inflammation, and collagen area, a marker of plaque stability in humans [28, 29]. In comparison to Baseline mice, the lesions of Resolution – Control and Resolution – β-carotene groups presented a reduction in CD68 content of approximately 36% and 45%, respectively (Figure 1I). The collagen content in lesions increased in both Resolution groups in comparison to Baseline, reaching statistical significance only in the β-carotene-fed mice. In this group, we observed 215% and 60% increase in collagen content compared to the Baseline and the Resolution – Control groups, respectively (Figure 1J). Lastly, we plotted the relative CD68 and collagen contents in the lesion to perform a descriptive discriminant analysis. Individual samples from three distinct experimental groups clustered together, highlighting significant differences between the three experimental groups for all the comparisons (Figure 1K).
To validate the results obtained in our ASO-LDLR reversible model of atherosclerosis, we utilized Ldlr-/- mice fed WD-VAD subjected to a dietary switch strategy to lower cholesterol in plasma and promote atherosclerosis resolution [18, 30]. Baseline Ldlr-/- mice were harvested after 12 weeks on WD-VAD, while the remaining animals were switched to either a Standard diet without vitamin A (Resolution – Control) or the same diet supplemented with β-carotene (Resolution – β-carotene) for four more weeks. To prevent changes in food intake due to consistency and hardness of the feed, we provided Standard diets as powder. This approach prevented a reduction in body weight, which could have resulted in confounding alterations in atherosclerosis resolution (Supplementary Figure 2A).
Ldlr-/- mice undergoing Resolution presented a reduction in total plasma cholesterol and triglyceride levels in comparison to Baseline mice. We did not observe changes in HDL-C levels between the tree experimental groups (Figure 2A). Systemic and hepatic vitamin A levels failed to show indications of vitamin A deficiency, and hepatic vitamin A stores increased in β-carotene-fed mice (Supplementary Figure 2B).
We next characterized atherosclerotic lesions at the level of the aortic root (Figure 2B). Lesion size area was comparable between experimental groups (Figure 2C), although CD68 content decreased to the same extent in both Resolution groups in comparison to Baseline mice (Figure 2D). In comparison to the Baseline group, collagen accumulation in the lesion increased 100% in the Resolution – Control and over 200% in the Resolution – β-carotene group, respectively (Figure 2E). Descriptive discriminant analysis showed comparable results to those observed for our ASO-LDLR model, where differences between the three experimental groups reached statistical significance (Figure 2F).
Together, these data show that β-carotene supplementation during atherosclerosis resolution results in the improvement of lesion composition in two independent mouse models.
3.2. BCO1 drives the effect of β-carotene on atherosclerosis resolution
To establish the contribution of BCO1 on the effect of β-carotene on atherosclerosis resolution, we utilized LDLR-ASO to promote atherogenesis in Bco1-/- mice following the same experimental approach described for wild-type mice (Figure 1A). Consistent with our results in wild-type mice, plasma cholesterol levels in both Resolution groups decreased in comparison to Baseline mice, while vitamin A measurements ruled out vitamin A deficiency (Supplementary Figure 3). The accumulation of β-carotene in tissues and plasma is characteristic in Bco1-/- mice [11]. Indeed, HPLC quantification of β-carotene in plasma and liver of Bco1-/- Resolution – β-carotene mice presented four-fold and 400-fold greater β-carotene levels found in wild-type Resolution – β-carotene, respectively (Figure 3A, B).
The characterization of the atherosclerotic lesions showed no alterations in lesion size between the three experimental groups (Figure 3C, D). When compared to Baseline mice, both Resolution groups displayed lower CD68 and higher collagen contents, although we didn’t observe differences in CD68 and collagen contents between both Resolution groups (Figure 3E, F). Descriptive discriminant analysis highlighted differences between Baseline Bco1-/- mice and their Resolution littermates, independently of the presence of β-carotene in the diet (Figure 3G).
3.3. Effect of β-carotene and anti-CD25 depletion on Treg cell number
Our data show that β-carotene favors atherosclerosis resolution in two independent mouse models (Figure 1K, 2F), and results in Bco1-/- mice directly implicate vitamin A formation in this process (Figure 3G). Retinoic acid is the transcriptionally active form of vitamin A and promotes Treg differentiation by upregulating FoxP3 expression in various experimental models [31–36]. Treg number decreases in developing lesions and increases during atherosclerosis resolution [6, 37, 38], but whether the dietary manipulation of β-carotene or vitamin A affects Treg number during atherosclerosis remains unanswered. To investigate whether the Tregs are responsible for the effect of dietary β-carotene on atherosclerosis resolution, we induced atherosclerosis in Foxp3EGFP mice by injecting ASO-LDLR as described above (Figure 1 and 3). Foxp3EGFP mice co-express EGFP and FoxP3 under the regulation of the endogenous FoxP3 promoter [39]. After 16 weeks on diet, mice undergoing resolution were treated twice with either the PC61 anti-CD25 monoclonal antibody (anti-CD25) or an isotype control (IgG) (Figure 4A) [6]. We did not observe changes in body weight among groups, and the three groups undergoing resolution showed a normalization in plasma lipids in comparison to Baseline controls (data not shown).
Flow cytometry analyses demonstrated the effectiveness of the anti-CD25 treatment by reducing the ratio of circulating and splenic CD25+FoxP3+ (CD25+ Tregs) in comparison to the other experimental groups (Figure 4B-D). We also observed a depletion of CD25+ Tregs and CD25+FoxP3- T cells in the lesion and lymph nodes (Figure 4E, F), in agreement with previous reports showing that anti-CD25 fails to completely deplete CD25-FoxP3+ Tregs (CD25- Tregs), which retain strong anti-inflammatory properties [7]. Hence, we quantified the number of total Tregs independently of the presence of CD25 by counting the number of GFP/FoxP3/DAPI triple positive cells (Figure 4G). All the groups undergoing Resolution presented a greater total Treg number than Baseline mice, although the results did not reach statistical significance between Baseline and Resolution – Control group (P = 0.10). Resolution – β-carotene injected with IgG presented the highest Treg cell number among all the other experimental groups, suggesting that dietary β-carotene favors Treg expansion in the plaque (Figure 4H).
Circulating total Treg number remained constant, but we observed a slight decrease in the number of splenic total Tregs in mice undergoing Resolution in comparison to Baseline mice. This reduction was more pronounced in the Resolution – β-carotene mice + anti-CD25 (Supplementary Figure 4A, B). The number of circulating CD25- Tregs increased in the Resolution – β-carotene mice + anti-CD25 group in comparison to Baseline mice, remaining constant in the spleen among all groups (Supplementary Figure 4C, D).
3.4. Anti-CD25 treatment partially abrogates the effect of β-carotene on atherosclerosis resolution
Tregs possess strong anti-inflammatory properties independently of the presence of CD25 [7, 40], and play an important role on plaque remodeling during atherosclerosis regression [6]. Hence, we evaluated plaque composition in our Foxp3EGFP mice (Figure 5A). As expected, all experimental groups showed comparable lesion size at the level of the aortic root (Figure 5B). Mice in the Resolution – β-carotene + IgG group displayed a reduction in CD68 content in the lesion of approximately 50% in comparison to Baseline mice. Resolution – Control + IgG and Resolution – β-carotene + anti-CD25 groups showed a 30% reduction in comparison to Baseline mice, although only the former reached statistical significance (Figure 5C). Collagen content in the lesion of Resolution – β-carotene + IgG mice was significantly higher in comparison to any other experimental group. Resolution Control + IgG and Resolution – β-carotene + Anti-CD25 showed comparable results, while Baseline mice had the lowest collagen content among all the groups (Figure 5D).
We next performed a descriptive discriminant analysis to examine pairwise comparisons between our four experimental groups. The Baseline group was significantly different in comparison to all the Resolution counterparts. Resolution – β-carotene + IgG mice were different from their Resolution – Control + IgG, as we observed in our two previous resolution experiments (Figure 1K and 2F). We did not observe statistical differences when we compared Resolution – β-carotene + anti-CD25 to Resolution – Control + IgG (FDR = 0.38) or Resolution – β-carotene + IgG to (FDR = 0.10) (Figure 5E).
The presence of anti-inflammatory macrophages in the lesions, together with a net egress of pro-inflammatory macrophages are key features of atherosclerosis resolution [41]. We quantified arginase 1 content in the lesion, a key anti-inflammatory marker in mice during regression that is synergistically upregulated in anti-inflammatory macrophages exposed to retinoic acid [42, 43] (Figure 5F). Only those mice fed β-carotene, independent of the injection with IgG or anti-CD25, showed an upregulation of arginase 1 in the lesion (Figure 5G). We also evaluated macrophage egress by injecting a single dose of EdU a week before sacrificing the Baseline mice (see methods for details) (Figure 5H). Only those mice fed β-carotene, independent of the antibody treatment, displayed a greater egress in comparison to Baseline mice (Figure 5I). We did not observe changes in monocyte recruitment evaluated by injecting fluorescently labeled beads 24 h before the sacrifice (Figure 5J, K), nor changes in Ki67+CD68+ cells, as an indicator of macrophage proliferation in the lesion (Figure 5L, M).
4. Discussion
Seminal studies showed that β-carotene delays atherosclerosis progression in various experimental models by reducing plasma cholesterol levels [44–46]. In 2020, we demonstrated that these effects depend on BCO1 activity in mice, and that a genetic variant in the BCO1 gene is associated with a reduction in plasma cholesterol levels in people [15, 17]. Our study shows that β-carotene promotes atherosclerosis resolution in two independent experimental models in a BCO1-dependent manner. Treg depletion studies revealed that dietary β-carotene favors Treg expansion in resolving lesions. Together, these findings identify dietary β-carotene and its conversion to vitamin A as a promising strategy to ameliorate plaque burden not only by delaying atherosclerosis progression, but also by reversing atherosclerosis inflammation.
Carotenoids are the main source of vitamin A in human diet, and the only source of this vitamin in strict vegetarians [47]. Among those carotenoids with provitamin A activity, β-carotene is the most abundant in our diet and the only compound capable of producing two vitamin A molecules. Vitamin A is required for vision, embryo development, and immune cell maturation, making β-carotene a crucial nutrient for human health [48]. Unlike preformed vitamin A, the intestinal uptake of carotenoids is a protein-mediated process that depends on vitamin A status. This regulatory mechanism prevents the excessive uptake of provitamin A carotenoids, contributing to preventing vitamin A toxicity [49, 50].
BCO1 is the only enzyme in mammals capable of synthetizing vitamin A from carotenoids [10, 12]. Therefore, it is not surprising that SNPs in the BCO1 gene are associated to alterations in circulating carotenoids including β-carotene [51–53]. We recently described that subjects harboring at least a copy of rs6564851-T allele, which increases BCO1 activity [54], show a reduction in total cholesterol and non-HDL-C in comparison to those with two copies of the rs6564851-G variant [17]. A recent study revealed that this variant is also associated with triglyceride levels in middle-aged individuals [55], implicating BCO1 activity as a novel regulator of plasma lipid profile. These studies provide a clinical relevance to studies performed in rodents and rabbits in which β-carotene-rich diets reduce plasma cholesterol and mitigate the development of atherosclerosis [15, 44–46].
Carotenoids, including β-carotene, possess antioxidant properties in lipid-rich environments [56]. The development of Bco1-/- mice of contributed to solving a long-lasting controversy in the carotenoid field by dissecting the biological effects of intact β-carotene and its role in vitamin A formation. When Bco1-/- mice are fed β-carotene, these mice accumulate large amounts of this compound in tissues and plasma [11]. In 2011, we reported that wild-type mice fed β-carotene exhibited a reduction in adipose tissue size. Bco1-/- mice subjected to the same experimental conditions did not chow differences in adipose tissue size in comparison to control-fed mice despite accumulating large amounts of β-carotene in this tissue [16]. We recently over-expressed BCO1 in the adipose tissue of Bco1-/- mice fed β-carotene. Under these conditions, we observed an increase in vitamin A levels including retinoic acid, and a reduction of adipose tissue size [16]. These effects are in line with those reported by Palou’s group utilizing both dietary vitamin A and retinoic acid supplementation, which promotes fatty acid oxidation and thermogenesis in various experimental models [57–67].
In 2020, we confirmed the implication of BCO1 activity and vitamin A in the development of atherosclerosis. We compared the effect of β-carotene on Ldlr-/- and Ldlr-/-Bco1-/- mice using the same experimental diets utilized in this study (Supplementary Table 1). In alignment with our clinical data, β-carotene reduced total cholesterol and non-HDL-C in Ldlr-/- mice, but not in Ldlr-/-Bco1-/- mice [15, 17]. Direct administration of retinoic acid caused a reduction in cholesterol and triglyceride secretion in both cultured hepatocytes and mice, while bone marrow transplant experiments showed a moderate effect of BCO1 activity in myeloid cells [15]. Whether BCO1 activity is associated with the development of atherosclerotic cardiovascular disease in humans, however, remains unexplored.
Besides its effects on lipid metabolism, retinoic acid modulates immune cell function [68]. Exogenous retinoic acid promotes alternative macrophage activation in various cell culture models, and skews naïve T cells to anti-inflammatory Tregs by directly upregulating the transcription factor FoxP3 [69, 70]. The expression of FoxP3 is necessary and sufficient for the anti-inflammatory phenotype of Tregs [8, 71]. Studies carried out by Loke’s group highlighted the interplay between alternative macrophage activation and Treg differentiation, a process that was proposed to be mediated by the production and release of retinoic acid by the macrophage [33, 36]. This hypothesis has not been demonstrated to date, partially due to the technical difficulty to quantify retinoic acid production in biological samples [72]. We recently overcame this limitation and demonstrated for the first time that alternatively-activated macrophages produce and release retinoic acid in a STAT6-dependent manner [43]. We also demonstrated that exogenous retinoic synergizes with interleukin 4 (IL4) to stimulate the expression of anti-inflammatory genes in the macrophage, including arginase 1. More importantly, we observed that macrophages exposed to both retinoic acid and IL4 displayed greater efferocytosis and lysosomal activities than those exposed to IL4 or retinoic acid alone [43]. These results indicate that the combination of retinoic acid with anti-inflammatory signals typically present during inflammatory resolution such as IL4 could favor atherosclerosis resolution. It remains unanswered whether retinoic acid released by the macrophage is sufficient to skew naïve T cells to Tregs in the lesion by upregulating FoxP3 expression alone.
Our experiment using Foxp3EGFP mice show that β-carotene supplementation caused Treg expansion in regressing lesions. To our knowledge, this is the first report showing that a dietary intervention with a nutrient administered at physiological concentrations can modulate Treg levels in the atherosclerotic lesion. As a reference, our diets were supplemented with 50 mg of β-carotene/kg in comparison to 80 mg of β-carotene/kg in carrots (USDA Database). Additionally, we provided these diets in mice that were not deficient in vitamin A, as our HPLC data show (Figure 1E, F and Supplementary Figure 2B, C), for a relatively short period of time (3 or 4 weeks).
To establish a direct link between the effect of β-carotene supplementation and Tregs in our experimental model, we decided to deplete Tregs in Foxp3EGFP mice by infusing them with anti-CD25, following Sharma and colleagues’ approach [6]. However, our data show that this strategy failed to completely deplete Tregs, as previously reported by other investigators [7, 40]. CD25- Tregs remained in circulation and tissues including aortic lesions (Figure 4E-H and Supplementary Figure 4). It is possible that the conversion of β-carotene to retinoic acid favored Treg expansion by specifically favoring CD25- Treg proliferation, which are insensitive to anti-CD25. Whether β-carotene supplementation during atherosclerosis resolution alters Treg content in other organs and disease models were outside of the scope of this study. For example, an increase in Treg number in developing tumors could result in the reprograming of pro-inflammatory macrophages towards resolving macrophages that could contribute to tumor expansion [73]. In summary, partial Treg depletion was sufficient to mitigate the effects of β-carotene on plaque composition during the resolution of atherosclerosis, providing a direct link between β-carotene and Treg number (Figure 5A-G).
Another question remains unanswered: What is the source of vitamin A that favors Treg expansion in the lesion? Our HPLC analyses show that circulating β-carotene in wild-type mice is marginal, although hepatic vitamin A stores highlight an increase in vitamin A formation (Figure 1F and Figure 3A, B). It is not clear whether naïve T cells express BCO1, which would enable them to locally produce vitamin A and its derivative retinoic acid. Previous work has related tissue macrophages as the responsible for retinoic acid production and suggested that these cells would release it to signal nearby naïve T cells that in turn, could differentiate into Tregs. Retinoic acid could be originated from β-carotene or retinol/retinyl esters stored in the cell, although our RNA sequencing analysis revealed that BCO1 expression in plaque macrophages is relatively limited [15]. Plaque macrophages, and T cells in a lesser extent, express various scavenger receptors that have been linked to the uptake of retinoids and carotenoids such as the scavenger receptor class BI, lipoprotein lipase and the cluster of differentiation 36 [74]. Determining whether naïve T cells rely on plaque macrophages to obtain retinoids and activate FoxP3 to differentiate into Treg is not clear to this day.
In summary, we report for the first time that vitamin A production from β-carotene favors Treg expansion in the atherosclerotic lesion, a process that contributes to atherosclerosis resolution. Together with the cholesterol-lowering effects of β-carotene described in the past, unveils a dual role of dietary β-carotene and the enzyme BCO1: (1) BCO1 delays atherosclerosis progression by reducing plasma cholesterol, and (2) favor atherosclerosis resolution by modulating Treg levels and macrophage polarization status.
Supplementary Figures
References
- 1.Vulnerable atherosclerotic plaque metalloproteinases and foam cell phenotypesThrombosis and haemostasis 101:1006–1011
- 2.Atherosclerosis: Making a U TurnAnnu Rev Med 71:191–201
- 3.Adaptive immunity and atherosclerosisClinical Immunology 134:33–46
- 4.The influence of innate and adaptive immune responses on atherosclerosisAnnual review of pathology 9:73–102
- 5.Depletion of regulatory T cells in tumors with an anti-CD25 immunotoxin induces CD8 T cell-mediated systemic antitumor immunityProc Natl Acad Sci U S A 116:4575–4582
- 6.Regulatory T Cells License Macrophage Pro-Resolving Functions During Atherosclerosis RegressionCirc Res 127:335–353
- 7.Incomplete depletion and rapid regeneration of Foxp3+ regulatory T cells following anti-CD25 treatment in malaria-infected miceJ Immunol 178:4136–46
- 8.Regulatory T cell lineage specification by the forkhead transcription factor foxp3Immunity 22:329–41
- 9.Retinoic acid inhibits Th17 polarization and enhances FoxP3 expression through a Stat-3/Stat-5 independent signaling pathwayBlood 111:1013–20
- 10.Filling the gap in vitamin A research. Molecular identification of an enzyme cleaving beta-carotene to retinalJ Biol Chem 275:11915–20
- 11.CMO1 deficiency abolishes vitamin A production from beta-carotene and alters lipid metabolism in miceJ Biol Chem 282:33553–61
- 12.Two carotenoid oxygenases contribute to mammalian provitamin A metabolismJ Biol Chem 288:34081–96
- 13.Beta-carotene reduces body adiposity of mice via BCMO1PLoS One 6
- 14.Beta,beta-carotene decreases peroxisome proliferator receptor gamma activity and reduces lipid storage capacity of adipocytes in a beta,beta-carotene oxygenase 1-dependent mannerJ Biol Chem 285:27891–9
- 15., beta-carotene conversion to vitamin A delays atherosclerosis progression by decreasing hepatic lipid secretion in miceJ Lipid Res
- 16.The conversion of beta-carotene to vitamin A in adipocytes drives the anti-obesogenic effects of beta-carotene in miceMol Metab 101640
- 17., beta-Carotene Oxygenase 1 Activity Modulates Circulating Cholesterol Concentrations in Mice and HumansJ Nutr
- 18.Short-Term Acyl-CoA:Cholesterol Acyltransferase Inhibition, Combined with Apoprotein A1 Overexpression, Promotes Atherosclerosis Inflammation Resolution in MiceMol Pharmacol 99:175–183
- 19.Atherosclerosis Regression and Cholesterol Efflux in Hypertriglyceridemic MiceCirc Res 128:690–705
- 20.Neutrophil extracellular traps promote macrophage inflammation and impair atherosclerosis resolution in diabetic miceJCI Insight 5
- 21.Apolipoprotein AI) Promotes Atherosclerosis Regression in Diabetic Mice by Suppressing Myelopoiesis and Plaque InflammationCirculation 140:1170–1184
- 22.Novel Reversible Model of Atherosclerosis and Regression Using Oligonucleotide Regulation of the LDL ReceptorCirculation Research 122:560–567
- 23.Methods to Study Monocyte and Macrophage Trafficking in Atherosclerosis Progression and ResolutionMethods Mol Biol 1951:153–165
- 24.Controlling the false discovery rate in behavior genetics researchBehav Brain Res 125:279–84
- 25.Retinoic acid-metabolizing enzyme Cyp26a1 is essential for determining territories of hindbrain and spinal cord in zebrafishDev Biol 278:415–27
- 26.Differential expression of the retinoic acid-metabolizing enzymes CYP26A1 and CYP26B1 during murine organogenesisMech Dev 110:173–7
- 27.Novel Reversible Model of Atherosclerosis and Regression Using Oligonucleotide Regulation of the LDL ReceptorCirc Res 122:560–567
- 28.Stabilization of atherosclerotic plaques: New mechanisms and clinical targetsNature Medicine 8:1257–1262
- 29.Targeting inflammation in atherosclerosis – from experimental insights to the clinicNat Rev Drug Discov 20:589–610
- 30.Targeted Nanotherapeutics Encapsulating Liver X Receptor Agonist GW3965 Enhance Antiatherogenic Effects without Adverse Effects on Hepatic Lipid Metabolism in Ldlr(-/-) MiceAdv Healthc Mater 6
- 31.Vitamin A mediates conversion of monocyte-derived macrophages into tissue-resident macrophages during alternative activationNat Immunol 18:642–653
- 32.MicroRNA-33-dependent regulation of macrophage metabolism directs immune cell polarization in atherosclerosisJ Clin Invest 125:4334–48
- 33.Alternatively activated macrophages derived from monocytes and tissue macrophages are phenotypically and functionally distinctBlood 123:e110–22
- 34.Ly6Chigh monocytes become alternatively activated macrophages in schistosome granulomas with help from CD4+ cellsPLoS Pathog 10
- 35.Immune regulation during helminth infectionsPLoS Pathog 9
- 36.Upregulation of retinal dehydrogenase 2 in alternatively activated macrophages during retinoid-dependent type-2 immunity to helminth infection in micePLoS Pathog 8
- 37.Treating atherosclerosis with regulatory T cellsArterioscler Thromb Vasc Biol 35:280–7
- 38.Natural regulatory T cells control the development of atherosclerosis in miceNat Med 12:178–80
- 39.Regulatory T cells dynamically control the primary immune response to foreign antigenJ Immunol 178:2961–72
- 40.Regulatory T Cells Maintain Selective Access to IL-2 and Immune Homeostasis despite Substantially Reduced CD25 FunctionJ Immunol 205:2667–2678
- 41.Macrophage Trafficking, Inflammatory Resolution, and Genomics in Atherosclerosis: JACC Macrophage in CVD Series (Part 2)J Am Coll Cardiol 72:2181–2197
- 42.Macrophage Metabolism of Apoptotic Cell-Derived Arginine Promotes Continual Efferocytosis and Resolution of InjuryCell Metab 31:518–533
- 43.Functional characterization of interleukin 4 and retinoic acid signaling crosstalk during alternative macrophage activationBiochim Biophys Acta Mol Cell Biol Lipids 159291
- 44.Vitamin A-deficient diet accelerated atherogenesis in apolipoprotein E(-/-) mice and dietary beta-carotene prevents this consequenceBiomed Res Int
- 45.A 9-cis beta-carotene-enriched diet inhibits atherogenesis and fatty liver formation in LDL receptor knockout miceJ Nutr 138:1923–30
- 46.Beta-carotene inhibits atherosclerosis in hypercholesterolemic rabbitsJ Clin Invest 96:2075–82
- 47.Beta-carotene is an important vitamin A source for humansJ Nutr 140:2268–2285
- 48.Amengual, beta-carotene in Obesity Research: Technical Considerations and Current Status of the FieldNutrients 11
- 49.Genetics and diet regulate vitamin A production via the homeobox transcription factor ISXJ Biol Chem 288:9017–27
- 50.Isx participates in the maintenance of vitamin A metabolism by regulation of beta-carotene 15,15’-monooxygenase (Bcmo1) expressionJ Biol Chem 283:4905–11
- 51.Single nucleotide polymorphisms in CETP, SLC46A1, SLC19A1, CD36, BCMO1, APOA5, and ABCA1 are significant predictors of plasma HDL in healthy adultsLipids Health Dis 12
- 52.Common SNP rs6564851 in the BCO1 Gene Affects the Circulating Levels of beta-Carotene and the Daily Intake of Carotenoids in Healthy Japanese WomenPLoS One 11
- 53.Single Nucleotide Polymorphisms in beta-Carotene Oxygenase 1 are Associated with Plasma Lycopene Responses to a Tomato-Soy Juice Intervention in Men with Prostate CancerJ Nutr 149:381–397
- 54.Single nucleotide polymorphisms upstream from the beta-carotene 15,15’-monoxygenase gene influence provitamin A conversion efficiency in female volunteersJ Nutr 142:161–5
- 55.Common variant rs6564851 near the beta-carotene oxygenase 1 gene is associated with plasma triglycerides levels in middle-aged Mexican men adultsNutr Res 103:30–39
- 56.A global perspective on carotenoids: Metabolism, biotechnology, and benefits for nutrition and healthProg Lipid Res 70:62–93
- 57.Carotenoids and carotenoid conversion products in adipose tissue biology and obesity: Pre-clinical and human studiesBiochim Biophys Acta Mol Cell Biol Lipids 158676
- 58.Retinoic Acid Increases Fatty Acid Oxidation and Irisin Expression in Skeletal Muscle Cells and Impacts Irisin In VivoCell Physiol Biochem 46:187–202
- 59.Vitamin A supplementation in early life affects later response to an obesogenic diet in ratsInt J Obes (Lond 37:1169–76
- 60.Induction of carnitine palmitoyl transferase 1 and fatty acid oxidation by retinoic acid in HepG2 cellsInt J Biochem Cell Biol 44:2019–27
- 61.Retinoic acid treatment enhances lipid oxidation and inhibits lipid biosynthesis capacities in the liver of miceCell Physiol Biochem 25:657–66
- 62.Retinoic acid treatment increases lipid oxidation capacity in skeletal muscle of miceObesity (Silver Spring 16:585–91
- 63.Remodeling of white adipose tissue after retinoic acid administration in miceEndocrinology 147:5325–32
- 64.Effects of retinoic acid administration and dietary vitamin A supplementation on leptin expression in mice: lack of correlation with changes of adipose tissue mass and food intakeBiochim Biophys Acta 1740:258–65
- 65.Modulation of resistin expression by retinoic acid and vitamin A statusDiabetes 53:882–9
- 66.In vitro and in vivo induction of brown adipocyte uncoupling protein (thermogenin) by retinoic acidBiochem J 317:827–33
- 67.All-trans-retinoic acid represses obesity and insulin resistance by activating both PPAR{beta}/{delta} and RARMol Cell Biol
- 68.The role of beta-carotene and vitamin A in atherogenesis: Evidences from preclinical and clinical studiesBiochim Biophys Acta Mol Cell Biol Lipids 158635
- 69.Global characterization of macrophage polarization mechanisms and identification of M2-type polarization inhibitorsCell Rep 37
- 70.Reciprocal TH17 and regulatory T cell differentiation mediated by retinoic acidScience 317:256–60
- 71.Control of regulatory T cell development by the transcription factor Foxp3Science 299:1057–61
- 72.Quantitative profiling of endogenous retinoic acid in vivo and in vitro by tandem mass spectrometryAnal Chem 80:1702–8
- 73.Regulatory T (Treg) cells in cancer: Can Treg cells be a new therapeutic target?Cancer Sci 110:2080–2089
- 74.Mechanisms of Carotenoid Intestinal Absorption: Where Do We Stand?Nutrients 11
Article and author information
Author information
Version history
- Sent for peer review:
- Preprint posted:
- Reviewed Preprint version 1:
- Reviewed Preprint version 2:
- Version of Record published:
- Version of Record updated:
Copyright
© 2023, Pinos 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.
Metrics
- views
- 1,280
- downloads
- 152
- citations
- 2
Views, downloads and citations are aggregated across all versions of this paper published by eLife.