Amphiphysin IIm, a novel amphiphysin II isoform, is required for macrophage phagocytosis

被引:62
作者
Gold, ES
Morrissette, NS
Underhill, DM
Guo, J
Bassetti, M
Aderem, A [1 ]
机构
[1] Univ Washington, Dept Immunol, Seattle, WA 98159 USA
[2] Univ Washington, Div Cardiol, Seattle, WA 98159 USA
关键词
D O I
10.1016/S1074-7613(00)80181-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Phagocytosis of pathogens by macrophages initiates the innate immune response, which in turn orchestrates the adaptive immune response. Amphiphysin II participates in receptor-mediated endocytosis, in part, by recruiting the GTPase dynamin to the nascent endosome. We demonstrate here that a novel isoform of amphiphysin II associates with early phagosomes in macrophages. We have ablated the dynamin-binding site of this protein and shown that this mutant form of amphiphysin II inhibits phagocytosis at the stage of membrane extension around the bound particles. We define a signaling cascade in which PI3K is required to recruit amphiphysin II to the phagosome, and amphiphysin II in turn recruits dynamin. Thus, amphiphysin II facilitates a critical initial step in host response to infection.
引用
收藏
页码:285 / 292
页数:8
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