生物
基因
心力衰竭
癌症研究
炎症
内科学
疾病
发病机制
免疫学
基因表达
信号转导
免疫系统
下调和上调
作者
Xiang Chen,Kaja S. Arusha,Danielle Springer,Sachiko Nakamori,Jing Cui,Ping Du Jiang,Zhi-Hong Yang,Yu Zhang,Huie Jing,Ann Y. Park,Maria H Zhu,Sarah E. Weber,Deniz N Cağdaş,Hassan Abolhassani,Nasrin Behniafard,Margery G. Smelkinson,Qihui Liang,Elif Everest,Julia F. Kun,Alyssa Grogan
出处
期刊:Cell
[Cell Press]
日期:2026-10-01
卷期号:189 (21): 6792-6809.e21
标识
DOI:10.1016/j.cell.2026.09.032
摘要
Controlling hyperlipidemia has reduced but not eliminated atherosclerotic cardiovascular disease (ASCVD) as a major cause of human mortality. Here, we report that loss of the immunoregulatory gene GTPase of immunity-associated protein 6 (Gimap6) in mice causes an inflammatory vasculopathy and accelerated atherosclerosis in the absence of hyperlipidemia. These vascular abnormalities cause progressive cardiac ischemia, myocardial infarction, and heart failure, culminating in early death. GIMAP6 loss precipitates early endothelial barrier failure and a mitochondrial reactive oxygen species (ROS)-PPARγ-CD36 lipid-influx cascade that lowers the threshold for foam-cell formation and induces IL-6/MCP-1/TNF-mediated inflammation. Human hypomorphic GIMAP6 variants, including the African-ancestry-enriched V65I allele, are associated with altered monocyte redox balance, increased CD36-mediated lipid uptake, and early ASCVD. Thus, GIMAP6 is a crucial safeguard for vascular integrity that restrains endothelial dysfunction, macrophage foam cell generation, and inflammation that can cause lethal ASCVD independently of systemic hyperlipidemia.
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