Perforin is recaptured by natural killer cells following target cells stimulation for cytotoxicity

被引:3
|
作者
Wang, Lei [1 ,2 ]
Sun, Rulin [1 ]
Li, Pan [1 ]
Han, Yang [1 ]
Xiong, Ping [1 ]
Xu, Yong [1 ]
Fang, Min [1 ]
Tan, Zheng [1 ]
Zheng, Fang [1 ]
Gong, Feili [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Immunol, Wuhan 430030, Peoples R China
[2] Hubei Univ Chinese Med, Inst Lab Med, Wuhan 430065, Peoples R China
关键词
clathrin; early endosome; endocytosis; natural killer cells; perforin; PLASMA-MEMBRANE-REPAIR; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SECRETORY LYSOSOMES; T-LYMPHOCYTES; IN-VITRO; NK CELLS; CAVEOLAE; EXPRESSION; CTL; APOPTOSIS;
D O I
10.1042/CBI20110242
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
When encountering target cells, NK (natural killer) cells exocytose Pfn (perforin) and granzyme B to kill challengers. We previously reported that granzyme B is recycled and reused by NK cells via clathrin-dependent endocytosis. However, whether Pfn, a main secretory vesicle content, indispensible to granzyme B killing, undergoes endocytosis remains unknown. We demonstrate that Pfn is recaptured by early endosomes of NK cells via a clathrin-dependent endocytosis after target cell stimulation. Inhibition of clathrin-dependent endocytosis significantly attenuated the cytotoxicity of NK cells. The data suggest that the recovery of Pfn contributes to the cytotoxicity of NK cells. The assay of endocytosis of lytic molecule presents a particular focus for exploring the mechanism of abnormal cytotoxicity of NK cells.
引用
收藏
页码:223 / 228
页数:6
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