ABCA1
炎症
巨噬细胞
胆固醇
流出
胆固醇逆向转运
泡沫电池
增强子
细胞生物学
医学
化学
生物
免疫学
内科学
生物化学
基因表达
体外
基因
脂蛋白
运输机
作者
Jing Wang,Qianqian Xiao,Yuwei Cai,Man Wang,Chen Chen,Luyun Wang,Ruiying Ma,Yanyan Cao,Yan Wang,Hu Ding,Dao Wen Wang
标识
DOI:10.1016/j.jacbts.2024.08.005
摘要
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 cis manner. Meanwhile, ABCA1-seRNA induced P65 ubiquitination degradation, and thereby repressed the macrophage inflammatory response. Consistently, overexpression of ABCA1-seRNA in ApoE-/- 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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