传出细胞增多
巨噬细胞
吞噬作用
医学
细胞生物学
炎症
免疫学
体外
生物
生物化学
化学
作者
Kyung‐Sun Heo,Hannah Cushman,Masashi Akaike,Chang-Hoon Woo,Xin Wang,Xing Qiu,Keigi Fujiwara,Jun‐ichi Abe
出处
期刊:Circulation
[Lippincott Williams & Wilkins]
日期:2014-04-29
卷期号:130 (2): 180-191
被引量:76
标识
DOI:10.1161/circulationaha.113.005991
摘要
Efferocytosis is a process by which dead and dying cells are removed by phagocytic cells. Efferocytosis by macrophages is thought to curb the progression of atherosclerosis, but the mechanistic insight of this process is lacking.When macrophages were fed apoptotic cells or treated with pitavastatin in vitro, efferocytosis-related signaling and phagocytic capacity were upregulated in an ERK5 activity-dependent manner. Macrophages isolated from macrophage-specific ERK5-null mice exhibited reduced efferocytosis and levels of gene and protein expression of efferocytosis-related molecules. When these mice were crossed with low-density lipoprotein receptor(-/-) mice and fed a high-cholesterol diet, atherosclerotic plaque formation was accelerated, and the plaques had more advanced and vulnerable morphology.Our results demonstrate that ERK5, which is robustly activated by statins, is a hub molecule that upregulates macrophage efferocytosis, thereby suppressing atherosclerotic plaque formation. Molecules that upregulate ERK5 and its signaling in macrophages may be good drug targets for suppressing cardiovascular diseases.
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