胞浆
生物
内体
细菌外膜
细胞生物学
脂多糖
内吞作用
革兰氏阴性菌
效应器
小泡
微生物学
生物化学
免疫学
膜
大肠杆菌
细胞内
细胞
酶
基因
作者
Sivapriya Kailasan Vanaja,Ashley J. Russo,Bharat Behl,Ishita Banerjee,Maya Yankova,Sachin D. Deshmukh,Vijay A. Rathinam
出处
期刊:Cell
[Cell Press]
日期:2016-05-01
卷期号:165 (5): 1106-1119
被引量:561
标识
DOI:10.1016/j.cell.2016.04.015
摘要
Sensing of lipopolysaccharide (LPS) in the cytosol triggers caspase-11 activation and is central to host defense against Gram-negative bacterial infections and to the pathogenesis of sepsis. Most Gram-negative bacteria that activate caspase-11, however, are not cytosolic, and the mechanism by which LPS from these bacteria gains access to caspase-11 in the cytosol remains elusive. Here, we identify outer membrane vesicles (OMVs) produced by Gram-negative bacteria as a vehicle that delivers LPS into the cytosol triggering caspase-11-dependent effector responses in vitro and in vivo. OMVs are internalized via endocytosis, and LPS is released into the cytosol from early endosomes. The use of hypovesiculating bacterial mutants, compromised in their ability to generate OMVs, reveals the importance of OMVs in mediating the cytosolic localization of LPS. Collectively, these findings demonstrate a critical role for OMVs in enabling the cytosolic entry of LPS and, consequently, caspase-11 activation during Gram-negative bacterial infections.
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