Enterohemorrhagic Escherichia coli O157 outer membrane vesicles induce interleukin 8 production in human intestinal epithelial cells by signaling via Toll-like receptors TLR4 and TLR5 and activation of the nuclear factor NF-κB
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
PubMed
29934223
DOI
10.1016/j.ijmm.2018.06.004
PII: S1438-4221(18)30224-8
Knihovny.cz E-zdroje
- Klíčová slova
- Enterohemorrhagic Escherichia coli O157, Flagellin, Immunomodulation, Lipopolysaccharide, Outer membrane vesicles, Proinflammatory cytokines,
- MeSH
- buněčná membrána metabolismus MeSH
- buňky HT-29 MeSH
- Caco-2 buňky MeSH
- epitelové buňky metabolismus MeSH
- Escherichia coli O157 patogenita MeSH
- faktory virulence metabolismus MeSH
- flagelin metabolismus MeSH
- infekce vyvolané Escherichia coli mikrobiologie patologie MeSH
- interleukin-8 biosyntéza MeSH
- lidé MeSH
- nádorové buněčné linie MeSH
- NF-kappa B metabolismus MeSH
- proteiny vnější bakteriální membrány metabolismus MeSH
- proteiny z Escherichia coli metabolismus MeSH
- signální transdukce MeSH
- střevní sliznice cytologie mikrobiologie patologie MeSH
- toll-like receptor 4 metabolismus MeSH
- toll-like receptor 5 metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- CXCL8 protein, human MeSH Prohlížeč
- faktory virulence MeSH
- flagelin MeSH
- interleukin-8 MeSH
- NF-kappa B MeSH
- proteiny vnější bakteriální membrány MeSH
- proteiny z Escherichia coli MeSH
- TLR4 protein, human MeSH Prohlížeč
- TLR5 protein, human MeSH Prohlížeč
- toll-like receptor 4 MeSH
- toll-like receptor 5 MeSH
Proinflammatory cytokines play important roles in the pathogenesis of diseases caused by enterohemorrhagic Escherichia coli (EHEC) O157, but the spectrum of bacterial components involved in the proinflammatory responses is not fully understood. Here, we investigated the abilities of outer membrane vesicles (OMVs), nanoparticles released by EHEC O157 during growth, to induce production of proinflammatory cytokines in human intestinal epithelial cells. OMVs from both EHEC O157:H7 and sorbitol-fermenting (SF) EHEC O157:H- induced production of interleukin-8 (IL-8) in Caco-2, HCT-8, and HT-29 intestinal epithelial cell lines. H7 flagellin was the key IL-8-inducing component of EHEC O157:H7 OMVs, whereas cytolethal distending toxin V and O157 lipopolysaccharide (LPS) largely contributed to IL-8 production elicited by flagellin-lacking OMVs from SF EHEC O157:H-. The H7 flagellin-mediated signaling via Toll-like receptor (TLR) 5, and O157 LPS-mediated signaling via TLR4/MD-2 complex, which were followed by activation of the nuclear factor NF-κB were major pathways underlying IL-8 production induced by EHEC O157 OMVs. The proinflammatory and immunomodulatory capacities of EHEC O157 OMVs have pathogenetic implications and support the OMVs as suitable vaccine candidates.
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