Bacterial Outer Membrane Vesicles Mediate Cytosolic Localization of LPS and Caspase-11 Activation

被引:670
作者
Vanaja, Sivapriya Kailasan [1 ]
Russo, Ashley J. [1 ]
Behl, Bharat [1 ]
Banerjee, Ishita [1 ]
Yankova, Maya [2 ]
Deshmukh, Sachin D. [3 ]
Rathinam, Vijay A. K. [1 ]
机构
[1] UConn Hlth Sch Med, Dept Immunol, 263 Farmington Ave, Farmington, CT 06030 USA
[2] UConn Hlth Sch Med, Cent Electron Microscopy Facil, 263 Farmington Ave, Farmington, CT 06030 USA
[3] Jena Univ Hosp, Ctr Sepsis Control & Care, Erlanger Allee 101, D-07747 Jena, Germany
关键词
NONCANONICAL INFLAMMASOME ACTIVATION; LEGIONELLA-PNEUMOPHILA; ESCHERICHIA-COLI; ENVELOPE STRESS; HOST-DEFENSE; GASDERMIN D; RECOGNITION; MECHANISM; CELLS;
D O I
10.1016/j.cell.2016.04.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
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.
引用
收藏
页码:1106 / 1119
页数:14
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