Identification of cytoskeletal regulatory proteins required for efficient phagocytosis in Drosophila

被引:97
作者
Pearson, AM
Baksa, K
Rämet, M
Protas, M
McKee, M
Brown, D
Ezekowitz, RAB
机构
[1] Massachusetts Gen Hosp, Dept Pediat, Lab Dev Immunol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Program Membrane Biol, Boston, MA 02114 USA
关键词
cytoskeleton; Drosophila; innate immunity; phagocytosis;
D O I
10.1016/S1286-4579(03)00157-6
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 is a complex and apparently evolutionarily conserved process that plays a central role in the immune response to infection. By ultrastructural and functional criteria, Drosophila hemocyte (macrophage) phagocytosis resembles mammalian phagocytosis. Using a non-saturated forward genetic screen for larval hemocyte phagocytosis mutants, D-SCAR and profilin were identified as important regulators of phagocytosis in Drosophila. In both hemocytes ex vivo and the macrophage-like S2 cell line, lack of D-SCAR significantly decreased phagocytosis of Escherichia coli and Staphylococcus aureus. In contrast, profilin mutant hemocytes exhibited increased phagocytic activity. Analysis of double mutants suggests that D-SCAR and profilin interact during phagocytosis. Finally, RNA interference studies in S2 cells indicated that the D-SCAR homolog D-WASp also participates in phagocytosis. This study demonstrates that Drosophila provides a viable model system in which to dissect the complex interactions that regulate phagocytosis. (C) 2003 Published by Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:815 / 824
页数:10
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