β-carotene accelerates atherosclerosis resolution in wild-type mice infused with anti-sense oligonucleotide targeting the low-density lipoprotein receptor (ASO-LDLR).

(A) Four-week-old male and female wild-type mice were fed a purified Western diet deficient in vitamin A (WD-VAD) and injected with antisense oligonucleotide targeting the low-density lipoprotein receptor (ASO-LDLR) once a week for 16 weeks to induce atherosclerosis. After 16 weeks, a group of mice was harvested (Baseline) and the rest of the mice were injected once with sense oligonucleotide (SO-LDLR) to inactivate ASO-LDLR and promote atherosclerosis resolution. Mice undergoing resolution were either kept on the same diet (Resolution - Control) or switched to a Western diet supplemented with 50 mg/kg of β-carotene (Resolution - β- carotene) for three more weeks. (B) Plasma lipid levels at the moment of the sacrifice. (C) Cholesterol and (D) triglyceride distribution in FPLC-fractioned plasma (data pooled from five mice/group). (E) Relative LDLR mRNA, and (F) protein expressions in the liver. (G) Circulating vitamin A (all-trans retinol), and (H) hepatic retinyl ester stores determined by HPLC. (I) Representative images for macrophage (CD68+, top panels), and picrosirius staining to identify collagen using the bright-field (middle panels) or polarized light (bottom panels). (J) Plaque size, (K) relative CD68 content, and (L) collagen content in the lesion. (M) Descriptive discriminant analysis employing the relative CD68 and collagen contents in the lesion as variables highlighting the FDR for each comparison. Each dot in the plot represents an individual mouse (n = 10 to 12/group). Values are represented as means ± SEM. Statistical differences were evaluated using one-way ANOVA with Tukey’s multiple comparisons test. Differences between groups were considered significant with a p-value < 0.05. * p < 0.05; ** p < 0.01; *** p < 0.005; **** p < 0.001. Size bar = 200 µm.

β-carotene accelerates atherosclerosis resolution in low-density lipoprotein deficient (Ldlr-/-) mice subjected to dietary switch.

Four-week-old male and female Ldlr-/- mice were fed a purified Western diet deficient in vitamin A (WD-VAD) for 12 weeks to induce atherosclerosis. After 12 weeks, a group of mice was harvested (Baseline) and the rest of the mice were switched to a Standard diet (Resolution-Control) or the same diet supplemented with 50 mg/kg of β-carotene (Resolution-β-carotene) for four more weeks. (A) Total cholesterol plasma levels at the moment of the sacrifice. (B) Representative images for macrophage (CD68+, top panels), and picrosirius staining to identify collagen using the bright-field (middle panels) or polarized light (bottom panels). (C) Plaque size, (D) relative CD68 content, and (E) collagen content in the lesion. (F) Descriptive discriminant analysis employing the relative CD68 and collagen contents in the lesion as variables highlighting the FDR for each comparison. Each dot in the plot represents an individual mouse (n = 9 to 12/group). (A-E) Values are represented as means ± SEM. Statistical differences were evaluated using one-way ANOVA with Tukey’s multiple comparisons test. Differences between groups were considered significant with a p- value < 0.05. * p < 0.05; *** p < 0.005; **** p < 0.001. Size bar = 200 µm.

β-carotene supplementation does alter atherosclerosis resolution in β-carotene oxygenase 1-deficient (Bco1-/-) mice infused with ASO-LDLR.

Four-week-old male and female Bco1-/-mice were fed a purified Western diet deficient in vitamin A (WD-VAD) and injected with antisense oligonucleotide targeting the low-density lipoprotein receptor (ASO-LDLR) once a week for 16 weeks to induce the development of atherosclerosis. After 16 weeks, a group of mice was harvested (Baseline) and the rest of the mice were injected once with sense oligonucleotide (SO-LDLR) to block ASO-LDLR (Resolution). Mice undergoing resolution were either kept on the same diet (Resolution-Control) or switched to a Western diet supplemented with 50 mg/kg of β-carotene (Resolution-β-carotene) for three more weeks. (A) β-carotene levels in plasma and (B) liver at the sacrifice determined by HPLC. (C) Representative images for macrophage (CD68+, top panels), and picrosirius staining to identify collagen using the bright-field (middle panels) or polarized light (bottom panels). (D) Plaque size, (E) relative CD68 content, and (F) collagen content in the lesion. (G) Descriptive discriminant analysis employing the relative CD68 and collagen contents in the lesion as variables highlighting the FDR for each comparison. Each dot in the plot represents an individual mouse (n = 5 to 11/group). (A-F) Values are represented as means ± SEM. Statistical differences were evaluated using one-way ANOVA with Tukey’s multiple comparisons test. Differences between groups were considered significant with a p-value < 0.05. * p < 0.05; ** p < 0.01; *** p < 0.005; **** p < 0.001. Size bar = 200 µm.

Effect of anti-CD25 treatment on Treg number.

(A) Four-week-old male and female mice expressing enhanced green fluorescence protein (EGFP) under the control of the forkhead box P3 (Foxp3) promoter (Foxp3EGFP mice) were fed a purified Western diet deficient in vitamin A (WD-VAD) and injected with antisense oligonucleotide targeting the low-density lipoprotein receptor (ASO-LDLR) once a week for 16 weeks to induce the development of atherosclerosis. After 16 weeks, a group of mice was harvested (Baseline) and the rest of the mice were injected once with sense oligonucleotide (SO-LDLR) to block ASO-LDLR (Resolution). Mice undergoing resolution were either kept on the same diet (Resolution-Control) or switched to a Western diet supplemented with 50 mg/kg of β-carotene (Resolution-β-carotene) for three more weeks. An additional group of mice fed with β-carotene was injected twice before sacrifice with anti-CD25 monoclonal antibody to deplete Treg (Resolution-β-carotene+anti-CD25). The rest of the resolution groups were injected with IgG isotype control antibody. (B) Representative flow cytometry panels showing splenic CD25+FoxP3+ (CD25+ Treg) cells in mice injected with IgG or anti-CD25. (C) Quantification of the splenic and (D) circulating blood levels of CD25+ Treg cells determined by flow cytometry. (E) Representative confocal images show the presence of total Tregs (CD25-FoxP3+ + CD25+ Tregs) and CD25+FoxP3- T cells in the lesion of mice injected with IgG (left panel) or anti-CD25 (right panel). (F) Representative confocal images show the presence of total Tregs and CD25+FoxP3- T cells in lymph nodes of mice injected with IgG (left panel) or anti-CD25 (right panel). quantification of CD25+ Tregs in the lesions. (G) Representative confocal image and (H) quantification of total Tregs in the lesion. Each dot in the plot represents an individual mouse (n = 5 to 11 mice/group). Values are represented as means ± SEM. Statistical differences were evaluated using one-way ANOVA with Tukey’s multiple comparisons test. Differences between groups were considered significant with a p-value < 0.05. * p < 0.05; ** p < 0.01; *** p < 0.005; **** p < 0.001.

Effect of anti-CD25 treatment on lesion composition and monocyte/macrophage trafficking.

Four-week-old male and female expressing enhanced green fluorescence protein (EGFP) under the control of the forkhead box P3 (Foxp3) promoter (Foxp3EGFP mice) were fed a purified Western diet deficient in vitamin A (WD-VAD) and injected with antisense oligonucleotide targeting the low-density lipoprotein receptor (ASO-LDLR) once a week for 16 weeks to induce the development of atherosclerosis. After 16 weeks, a group of mice was harvested (Baseline) and the rest of the mice were injected once with sense oligonucleotide (SO-LDLR) to block ASO-LDLR (Resolution). Mice undergoing resolution were either kept on the same diet (Resolution-Control) or switched to a Western diet supplemented with 50 mg/kg of β-carotene (Resolution-β-carotene) for three more weeks. An additional group of mice fed with β-carotene was injected twice before sacrifice with anti-CD25 monoclonal antibody to deplete Treg (Resolution-β-carotene+anti-CD25). The rest of the resolution groups were injected with IgG isotype control antibody. To quantify macrophage egress and monocyte recruitment, we injected a dose of EdU at week 15 and fluorescently labeled beads two days before harvesting the mice, respectively (see methods for details). (A) Representative images for macrophage (CD68+, top panels), and picrosirius staining to identify collagen using the bright-field (middle panels) or polarized light (bottom panels). Size bar = 200 µm. (B) Plaque size, (C) relative CD68 content, and (D) collagen content in the lesion. (E) Descriptive discriminant analysis employing the relative CD68 and collagen contents in the lesion as variables highlighting the FDR for each comparison. (F) Representative confocal image showing arginase 1 (green), CD68 (red), and DAPI (blue) in the lesion. (G) relative arginase 1 area in the lesion. (H) Representative confocal image showing Cyp26b1 (green), CD68 (red), and DAPI (blue) in the lesion. (I) relative Cyp26b1 area in the lesion. (J) EdU+ macrophages were identified by the colocalization of EdU (green) and DAPI (blue) in CD68+ (red) cells. (K) Number of EdU+ macrophages in the lesion. (L) Newly recruited monocytes were identified, and (M) quantified by the presence of beads (green) on the lesion. Size bars = 50 µm. Each dot in the plot represents an individual mouse (n = 5 to 11 mice/group). Values are represented as means ± SEM. Statistical differences were evaluated using one-way ANOVA with Tukey’s multiple comparisons test. Differences between groups were considered significant with a p-value < 0.05. * p < 0.05; ** p < 0.01; *** p < 0.005; **** p < 0.001.