Department of Medical Chemistry, Graduate School of Medicine, Kyoto University, Yoshida-Konoe, Sakyo-ku, Kyoto, Kyoto 606-8501, Japan.
Science. 2013 Jul 26;341(6144):403-6. doi: 10.1126/science.1236758. Epub 2013 Jul 11.
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.
凋亡细胞的一个典型特征是细胞膜表面暴露磷脂酰丝氨酸(PtdSer),作为被吞噬的“吃我”信号。我们表明,Xk 家族蛋白 Xkr8 介导 PtdSer 暴露以响应凋亡刺激。在凋亡过程中,缺乏 Xkr8 的小鼠 Xkr8(-/-)细胞或 Xkr8 表达被高甲基化抑制的人癌细胞未能暴露 PtdSer,并且被吞噬细胞吞噬的效率较低。Xkr8 被半胱天冬酶直接激活,并且其功能需要半胱天冬酶-3 切割位点。CED-8,即秀丽隐杆线虫唯一的 Xk 家族同源物,也促进了凋亡 PtdSer 的暴露和细胞尸体的吞噬。因此,Xk 家族蛋白通过改变质膜中磷脂的分布,在促进吞噬死亡细胞方面具有进化保守的作用。