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Updated: Mar 8, 2026

Quantification of Atherosclerosis in Mice
Published on: June 12, 2019
Changes in CD4+CD25+ Tregs in the pathogenesis of atherosclerosis in ApoE-/- mice
Li Xue-Mei1, Chen Jie1, Dai Xuan1
1Department of Emergency, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Abstract:
The goal of this study was to observe the pathological characteristics of atherosclerotic plaques in the aortic walls of ApoE-/- and C57BL/6J mice and the changes of CD4+CD25+ regulatory T cells (Tregs) in atherosclerotic mice. Twenty ApoE-/- mice were split into high-fat diet (AH) and normal diet (AN) groups and 10 C57BL/6J male mice were designated as the control group (BN). The serum concentrations of IL-10 and TGF-β1 were detected by enzyme-linked immunosorbent assay; paraffin sections of the aorta were stained with hematoxylin & eosin, and morphometric parameters were measured using the Image Pro Plus 6.0 system. Verhoeff stain was used to observe the distribution of elastic fibers, and immunohistochemical staining was performed to verify the phenotype of the forkhead box protein 3 (Foxp3+) CD25+ cells in the atherosclerotic tissue. The proportion of CD4+CD25+ Tregs in the spleen was calculated by flow cytometry. The thickness of the intima, the intima/media ratio, the plaque area, and the plaque/lumen ratio of mice in AN group were significantly larger than those of mice in BN group. The thickness of the intima, the plaque area, and the plaque/lumen ratio of the mice in AH group were significantly increased compared with those of the AN group mice. The serum concentrations of IL-10 and TGF-β1 and the percentage of splenic CD4+CD25+ Tregs in AN group mice were significantly decreased compared with the control group. The serum concentrations of IL-10 and TGF-β1 and the percentage of splenic CD4+CD25+ Tregs in the mice in AH group were significantly decreased compared with those in AN group. The proportions of Foxp3+ and CD25+ cells within the total lymphocyte population were significantly decreased in AH group mice compared with those in AN group mice. Atherosclerosis in an experimental mouse model was correlated with Treg depletion in the lymphoid tissues and plaques, indicating the important antiatherosclerotic role of CD4+CD25+ Tregs. Impact statement In this article, we conclude that Tregs decreased with atherosclerosis (AS) as determined in ApoE knockout mice fed a high fat diet. It is an important matter for understanding the AS pathology.
Insights
Regulatory T cells (Tregs) depletion is linked to atherosclerosis progression in ApoE knockout mice. This study highlights the anti-atherosclerotic role of Tregs, crucial for understanding disease pathology.
Area of Science:
- Immunology
- Cardiovascular Biology
- Pathology
Background:
- Atherosclerosis (AS) is a chronic inflammatory disease characterized by plaque buildup in arteries.
- Regulatory T cells (Tregs) play a critical role in maintaining immune homeostasis and suppressing excessive inflammation.
- The specific role of Tregs in the development and progression of atherosclerosis requires further elucidation.
Purpose of the Study:
- To investigate the pathological characteristics of atherosclerotic plaques in ApoE knockout mice.
- To examine the changes in CD4+CD25+ regulatory T cells (Tregs) in the context of atherosclerosis.
- To determine the correlation between Treg levels and the severity of atherosclerotic lesions.
Main Methods:
- Utilized ApoE knockout mice on high-fat (AH) and normal (AN) diets, with C57BL/6J mice as controls (BN).
- Assessed serum IL-10 and TGF-β1 concentrations via ELISA.
- Analyzed aortic plaque morphology using H&E staining and morphometry.
- Examined elastic fiber distribution with Verhoeff stain and identified Foxp3+ cells via immunohistochemistry.
- Quantified splenic CD4+CD25+ Tregs using flow cytometry.
Main Results:
- Atherosclerotic plaque development (intima thickness, plaque area) was significantly increased in AN and AH groups compared to BN controls.
- High-fat diet exacerbated plaque progression in AH mice compared to AN mice.
- Serum IL-10, TGF-β1 levels, and splenic Treg percentages were significantly decreased in both AN and AH groups compared to controls.
- Treg levels further decreased in the AH group compared to the AN group.
- Reduced proportions of Foxp3+ and CD25+ cells were observed in AH mice.
Conclusions:
- Atherosclerosis in this experimental model is associated with Treg depletion in lymphoid tissues and plaques.
- CD4+CD25+ Tregs demonstrate a significant anti-atherosclerotic role.
- Treg dysfunction contributes to the pathogenesis of atherosclerosis, suggesting potential therapeutic targets.
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