生物
传出细胞增多
炎症
吞噬作用
受体
结肠炎
细胞生物学
RAC1
G蛋白偶联受体
免疫学
信号转导
细胞凋亡
巨噬细胞
生物化学
体外
作者
Ming‐Yue Wu,Er‐Jin Wang,Richard D. Ye,Jiahong Lu
出处
期刊:Autophagy
[Taylor & Francis]
日期:2024-02-05
卷期号:20 (6): 1442-1443
被引量:2
标识
DOI:10.1080/15548627.2024.2311548
摘要
LC3-associated phagocytosis (LAP) is an instrumental machinery for the clearance of extracellular particles including apoptotic cells for the alleviation of inflammation. While pharmacological approaches to modulate LAP for inflammation regulation have been poorly explored, in our study we identified a novel compound, columbamine (COL), which can trigger LAP and enhance efferocytosis in an animal model of colitis to attenuate inflammation. We found that COL directly binds to and biasedly activates FPR2 (formyl peptide receptor 2) to promote efferocytosis and alleviate colitis. Biochemically, COL induces an interaction between RAC1 and the PIK3C3/VPS34-RUBCN/RUBICON complex, stimulating LC3-associated efferocytosis. These findings provide a novel interpretation of the potential roles of LAP in regulating inflammatory bowel disease (IBD), reveal the relationship between G protein-coupled receptors (GPCRs) and LAP, and highlight the role of RAC1 in regulating the PIK3C3/VPS34-RUBCN complex in LAP.
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