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

机译:细菌外膜囊泡介导LPS和Caspase-11激活的胞质定位。

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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.
机译:胞浆中的脂多糖(LPS)感测触发caspase-11活化,对于宿主抵抗革兰氏阴性细菌感染和败血症的发病机制至关重要。然而,大多数激活caspase-11的革兰氏阴性细菌不是胞质的,这些细菌的LPS进入胞质溶胶中的caspase-11的机制仍然难以捉摸。在这里,我们确定革兰氏阴性细菌产生的外膜囊泡(OMVs)作为一种载体,可以在体外和体内将LPS传递到触发caspase-11-依赖效应子的胞质溶胶中。 OMV通过内吞作用而被内在化,并且LPS从早期的内体释放到细胞质中。降泡细菌突变体的使用,其产生OMV的能力受到损害,显示了OMV在介导LPS的胞质定位中的重要性。总的来说,这些发现证明了OMV在使LPS进入胞质中并因此在革兰氏阴性细菌感染过程中激活caspase-11活化方面起着至关重要的作用。

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