Distinct roles of class I and class III phosphatidylinositol 3-kinases in phagosome formation and maturation

被引:390
作者
Vieira, OV
Botelho, RJ
Rameh, L
Brachmann, SM
Matsuo, T
Davidson, HW
Schreiber, A
Backer, JM
Cantley, LC
Grinstein, S
机构
[1] Hosp Sick Children, Div Cell Biol, Cell Biol Program, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Dept Biochem, Toronto, ON M5G 1X8, Canada
[3] Univ Coimbra, Ctr Neurosci, P-3000 Coimbra, Portugal
[4] Harvard Univ, Inst Med, Beth Israel Deaconess Med Ctr, Div Signal Transduct, Boston, MA 02115 USA
[5] Free Univ Berlin, Inst Biochem, D-14195 Berlin, Germany
[6] Univ Cambridge, Addenbrookes Hosp, Wellcome Trust Ctr Mol Mech Dis, Cambridge CB2 2QQ, England
[7] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[8] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10032 USA
基金
英国惠康基金;
关键词
phagocytosis; phosphatidylinositol; FYVE domain; EEAl; lysosomes;
D O I
10.1083/jcb.200107069
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Phagosomes acquire their microbicidal properties by fusion with lysosomes. Products of phosphatidylinositol 3-kinase (PI 3-kinase) are required for phagosome formation, but their role in maturation is unknown. Using chimeric fluorescent proteins encoding tandem FYVE domains, we found that phosphatidylinositol 3-phosphate (PIMP) accumulates greatly but transiently on the phagosomal membrane. Unlike the 3'-phosphoinositides generated by class I PI 3-kinases which are evident in the nascent phagosomal cup, PI(3)P is only detectable after the phagosome has sealed. The class III PI 3-kinase VPS34 was found to be responsible for PI(3)P synthesis and essential for phagolysosome formation. In contrast, selective ablation of class I PI 3-kinase revealed that optimal phagocytosis, but not maturation, requires this type of enzyme. These results highlight the differential functional role of the two families of kinases, and raise the possibility that PI(3)P production by VPS34 may be targeted during the maturation arrest induced by some intracellular parasites.
引用
收藏
页码:19 / 25
页数:7
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