ABCA1-Super Enhancer RNA Promotes Cholesterol Efflux, Reduces Macrophage-Mediated Inflammation and Atherosclerosis

We describe a previously uncharacterized ATP-binding cassette A1 super enhancer RNA (ABCA1-seRNA)-mediated cholesterol efflux. In addition, it promoted macrophage inflammatory cytokine release, and was causally correlated with coronary artery disease severity. Mechanistically, ABCA1-seRNA upregulated cholesterol efflux by interacting with mediator complex subunit 23 and recruiting retinoid X receptor-alpha and liver X receptor-alpha to promote ABCA1 transcription in a <i>cis</i> manner. Meanwhile, ABCA1-seRNA induced P65 ubiquitination degradation, and thereby repressed the macrophage inflammatory response. Consistently, overexpression of ABCA1-seRNA in ApoE<sup>-/-</sup> mice decreased plasma lipids, cytokines, and atherosclerotic plaques. These findings indicate ABCA1-seRNA is a critical epigenetic regulator that maintains cholesterol homeostasis and modulates inflammation, thus promising a therapeutic target for atherosclerotic cardiovascular diseases.

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Publication Details

Journal
JACC Basic to Translational Science
Published
2024-10-09
DOI
https://doi.org/10.1016/j.jacbts.2024.08.005
Citations
10
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
2.34

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article

ABCA1-Super Enhancer RNA Promotes Cholesterol Efflux, Reduces Macrophage-Mediated Inflammation and Atherosclerosis

Luyun Wang, Dao Wen Wang, Hu Ding, Chen Chen et al.
10 citations
JACC Basic to Translational Science
RNA Research and Splicing
2.34
article

ABCA1-Super Enhancer RNA Promotes Cholesterol Efflux, Reduces Macrophage-Mediated Inflammation and Atherosclerosis

Luyun Wang, Dao Wen Wang, Hu Ding, Chen Chen, Qianqian Xiao, Yanyan Cao, Yuwei Cai, Man Wang, Yan Wang, Ruiying Ma, Jing Wang
article en
10 citations

Abstract

We describe a previously uncharacterized ATP-binding cassette A1 super enhancer RNA (ABCA1-seRNA)-mediated cholesterol efflux. In addition, it promoted macrophage inflammatory cytokine release, and was causally correlated with coronary artery disease severity. Mechanistically, ABCA1-seRNA upregulated cholesterol efflux by interacting with mediator complex subunit 23 and recruiting retinoid X receptor-alpha and liver X receptor-alpha to promote ABCA1 transcription in a <i>cis</i> manner. Meanwhile, ABCA1-seRNA induced P65 ubiquitination degradation, and thereby repressed the macrophage inflammatory response. Consistently, overexpression of ABCA1-seRNA in ApoE<sup>-/-</sup> mice decreased plasma lipids, cytokines, and atherosclerotic plaques. These findings indicate ABCA1-seRNA is a critical epigenetic regulator that maintains cholesterol homeostasis and modulates inflammation, thus promising a therapeutic target for atherosclerotic cardiovascular diseases.

JACC Basic to Translational ScienceVol. 9(12)
Tongji Hospital (CN), Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China, Huazhong University of Science and Technology, Tongji University, National Key Research and Development Program of China, Tongji Medical College, Huazhong University of Science and Technology
Openalex Percentile: Top 11%
RNA Research and Splicing
2.34
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