磷脂酶
磷脂酰丝氨酸
细胞生物学
吞噬作用
细胞凋亡
程序性细胞死亡
生物
细胞
半胱氨酸蛋白酶
秀丽隐杆线虫
癌细胞
磷脂
化学
遗传学
膜
癌症
基因
作者
Jun Suzuki,Daniel P. Denning,Eiichi Imanishi,H. Robert Horvitz,Shinji Nagata
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2013-07-26
卷期号:341 (6144): 403-406
被引量:448
标识
DOI:10.1126/science.1236758
摘要
A classic feature of apoptotic cells is the cell-surface exposure of phosphatidylserine (PtdSer) as an "eat me" signal for engulfment. We show that the Xk-family protein Xkr8 mediates PtdSer exposure in response to apoptotic stimuli. Mouse Xkr8(-/-) cells or human cancer cells in which Xkr8 expression was repressed by hypermethylation failed to expose PtdSer during apoptosis and were inefficiently engulfed by phagocytes. Xkr8 was activated directly by caspases and required a caspase-3 cleavage site for its function. CED-8, the only Caenorhabditis elegans Xk-family homolog, also promoted apoptotic PtdSer exposure and cell-corpse engulfment. Thus, Xk-family proteins have evolutionarily conserved roles in promoting the phagocytosis of dying cells by altering the phospholipid distribution in the plasma membrane.
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