Focal exocytosis of VAMP3-containing vesicles at sites of phagosome formation

被引:251
作者
Bajno, L
Peng, XR
Schreiber, AD
Moore, HP
Trimble, WS
Grinstein, S
机构
[1] Hosp Sick Children, Cell Biol Programme, Res Inst, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Dept Biochem, Toronto, ON M5G 1X8, Canada
[3] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[4] Univ Calif Berkeley, Dept Cell Biol, Berkeley, CA 94720 USA
关键词
cellubrevin; phagocytosis; macrophage; recycling endosomes; GFP;
D O I
10.1083/jcb.149.3.697
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Phagocytosis involves the receptor-mediated extension of plasmalemmal protrusions, called pseudopods, which fuse at their tip to engulf a particle. Actin polymerizes under the nascent phagosome and may propel the protrusion of pseudopods. Alternatively, membrane extension could result from the localized insertion of intracellular membranes into the plasmalemma next to the particle. Here we show focal accumulation of VAMP3-containing vesicles, likely derived from recycling endosomes, in the vicinity of the nascent phagosome. Using green fluorescent protein (GFP) as both a fluorescent indicator and an exofacial epitope tag, we show that polarized fusion of VAMP3 vesicles precedes phagosome sealing, It is therefore likely that targeted delivery of endomembranes contributes to the elongation of pseudopods, In addition to mediating pseudopod formation, receptor-triggered focal secretion of endosomes may contribute to polarized membrane extension in processes such as lamellipodial elongation or chemotaxis.
引用
收藏
页码:697 / 705
页数:9
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