拉布
吞噬小体
吞噬体
GTP酶
细胞生物学
生物
胞吐
调节器
吞噬作用
生物化学
膜
基因
作者
Pengfei Guo,Xiaochen Wang
出处
期刊:Small GTPases
[Informa]
日期:2010-11-01
卷期号:1 (3): 170-173
被引量:14
标识
DOI:10.4161/sgtp.1.3.14511
摘要
During apoptosis, apoptotic cells are recognized and quickly engulfed by phagocytes. The internalized cell corpses are enclosed within membrane-bound vesicles called phagosomes. Cell corpse degradation depends on the phagosomes undergoing a maturation process, but regulation of phagosomal maturation is not well understood. Recently, we identified C. elegans Rab GTPase 14 as a novel regulator of apoptotic cell degradation. Loss of rab-14 function affects several steps of phagosome maturation, causing accumulation of persistent cell corpses. RAB-14 and UNC-108 (Rab GTPase 2) function redundantly to regulate phagosome maturation. Three Rabs, RAB-14, UNC-108/RAB2 and RAB-7, act cooperatively to control phagolysosome formation. RAB-14 and UNC-108 recruit lysosomes, while RAB-7 mediates fusion of lysosomes to phagosomes. Our data thus reveal the sequential action of Rab GTPases in regulating tethering, docking and fusion of lysosomes to phagosomes.
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