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Updated: Sep 30, 2025

Cholesterol Efflux Assay
Published on: March 6, 2012
CTRP15 promotes macrophage cholesterol efflux and attenuates atherosclerosis by increasing the expression of ABCA1
Wei-Hua Tan1, Zheng-Liang Peng1, Ting You1
1Department of Emergency Medicine, The First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, 421001, Hunan, China.
Insights
C1q tumor necrosis factor-related protein 15 (CTRP15) reduces atherosclerosis by enhancing cholesterol removal. This myokine boosts HDL-C levels and reverse cholesterol transport, offering a potential therapeutic target for cardiovascular disease.
Area of Science:
- Cardiovascular Biology
- Metabolic Research
- Molecular Medicine
Background:
- C1q tumor necrosis factor-related protein 15 (CTRP15) is a myokine linked to cardiovascular disease.
- The specific role of CTRP15 in atherosclerosis remains largely uncharacterized.
Purpose of the Study:
- To elucidate the function of CTRP15 in the development of atherosclerosis.
- To investigate the molecular mechanisms underlying CTRP15's effects on atherosclerosis.
Main Methods:
- Apolipoprotein E-deficient (apoE-/-) mice were used to study atherosclerosis in vivo.
- Lentivirus-mediated CTRP15 overexpression was employed in both in vivo and in vitro models.
- Macrophage lipid accumulation and cholesterol efflux assays were performed.
- The T-cadherin/miR-101-3p/ABCA1 pathway was analyzed to understand the mechanism.
Main Results:
- CTRP15 overexpression significantly reduced atherosclerotic plaque burden in apoE-/- mice.
- CTRP15 enhanced reverse cholesterol transport (RCT) efficiency and increased high-density lipoprotein cholesterol (HDL-C) levels.
- In vitro, CTRP15 inhibited lipid accumulation and promoted cholesterol efflux from macrophages.
- CTRP15 upregulated T-cadherin, decreased miR-101-3p, and consequently increased ABCA1 expression, facilitating cholesterol efflux.
Conclusions:
- CTRP15 plays a protective role against atherosclerosis development.
- CTRP15 inhibits atherosclerosis by enhancing RCT and increasing HDL-C levels through the T-cadherin/miR-101-3p/ABCA1 pathway.
- Targeting CTRP15 presents a promising therapeutic strategy for atherosclerotic cardiovascular diseases.
Abstract:
C1q tumor necrosis factor-related protein 15 (CTRP15), a newly identified myokine, is closely implicated in cardiovascular disease. However, the role of CTRP15 in atherosclerosis is still unclear. This study aims to determine the role of CTRP15 in atherosclerosis and explore the underlying mechanisms. Our findings revealed that lentivirus-mediated CTRP15 overexpression significantly decreased atherosclerotic plaque lesions and increased reverse cholesterol transport (RCT) efficiency and circulating HDL-C levels in apolipoprotein E-deficient (apoE-/-) mice. Consistently, in vitro, overexpression of CTRP15 also inhibited intracellular lipid accumulation and promoted cholesterol efflux from macrophages. Mechanistically, CTRP15 decreased the expression of miR-101-3p by upregulating T-cadherin, thereby facilitating ABCA1 expression and cholesterol efflux. In summary, these data indicate that CTRP15 inhibits the development of atherosclerosis by enhancing RCT efficiency and increasing plasma HDL-C levels via the T-cadherin/miR-101-3p/ABCA1 pathway. Targeting CTRP15 may serve as a novel and promising therapeutic strategy for atherosclerotic cardiovascular diseases.
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