| Literature DB >> 29462003 |
Lan Gu1,2, Ran Meng1,2, Yiting Tang3,2, Kai Zhao1,2, Fang Liang1,2, Rui Zhang1,2, Qianqian Xue1,2, Fangping Chen1, Xianzhong Xiao4, Huadong Wang5, Haichao Wang6, Timothy R Billiar7, Ben Lu1,2,4,5.
Abstract
Outer membrane vesicles (OMVs), released by variety of bacteria, are membrane-enclosed entities enriched in microbial components, toxins, and virulent factors. OMVs could deliver lipopolysaccharide (LPS) into the cytosol of host cells and subsequently activate caspase-11, which critically orchestrates immune responses and mediates septic shock. Although it is known that caspase-11 is activated by intracellular LPS, how OMVs deliver LPS into the cytosol remains largely unknown. Here we show that the activation of toll-like receptor 4 (TLR4), a LPS receptor on the cytoplasmic membrane, licenses macrophages to transport LPS from OMVs into the cytosol through TIR domain-containing adaptor-inducing interferon-β (TRIF). TRIF-mediated cytosolic delivery of LPS from OMVs depends on the production of type 1 interferon and the expression of guanylate-binding proteins (GBPs). Deletion of TRIF or GBPs prevents pyroptosis and lethality induced by OMVs or OMVs-releasing Escherichia coli. Together, these findings provide novel insight into how host coordinates extracellular and intracellular LPS sensing to orchestrate immune responses during gram-negative bacterial infection.Entities:
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Year: 2019 PMID: 29462003 DOI: 10.1097/SHK.0000000000001129
Source DB: PubMed Journal: Shock ISSN: 1073-2322 Impact factor: 3.454