A process for controlling intracellular bacterial infections induced by membrane injury

被引:128
作者
Roy, D
Liston, DR
Idone, VJ
Di, A
Nelson, DJ
Pujol, C
Bliska, JB
Chakrabarti, S
Andrews, NW
机构
[1] Yale Univ, Sch Med, Sect Microbial Pathogenesis, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
[3] Univ Chicago, Dept Physiol & Pharmacol, Chicago, IL 60637 USA
[4] SUNY Stony Brook, Sch Med, Ctr Infect Dis, Dept Mol Genet & Microbiol, Stony Brook, NY 11794 USA
关键词
D O I
10.1126/science.1098371
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Strategies for inhibiting phagolysosome fusion are essential for the intracellular survival and replication of many pathogens. We found that the lysosomal synaptotagmin Syt VII is required for a mechanism that promotes phagolysosomal fusion and limits the intracellular growth of pathogenic bacteria. Syt VII was required for a form of Ca2+-dependent phagolysosome fusion that is analogous to Ca2+-regulated exocytosis of lysosomes, which can be triggered by membrane injury. Bacterial type III secretion systems, which permeabilize membranes and cause Ca2+ influx in mammalian cells, promote lysosomal exocytosis and inhibit intracellular survival in Syt VII +/+ but not -/- cells. Thus, the lysosomal repair response can also protect cells against pathogens that trigger membrane permeabilization.
引用
收藏
页码:1515 / 1518
页数:4
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