| Literature DB >> 27810946 |
Dmitry Ratner1, M Pontus A Orning1,2, Egil Lien3,2.
Abstract
Innate immunity is critical for host defenses against pathogens, but many bacteria display complex ways of interacting with innate immune signaling, as they may both activate and evade certain pathways. Gram-negative bacteria can exhibit specialized nanomachine secretion systems for delivery of effector proteins into mammalian cells. Bacterial types III, IV, and VI secretion systems (T3SS, T4SS, and T6SS) are known for their impact on caspase-1-activating inflammasomes, necessary for producing bioactive inflammatory cytokines IL-1β and IL-18, key participants of anti-bacterial responses. Here, we discuss how these secretion systems can mediate triggering and inhibition of inflammasome signaling. We propose that a fine balance between secretion system-mediated activation and inhibition can determine net activation of inflammasome activity and control inflammation, clearance, or spread of the infection. © Society for Leukocyte Biology.Entities:
Keywords: Interleukin-18; Interleukin-1beta; caspase-1; pyroptosis
Mesh:
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Year: 2016 PMID: 27810946 PMCID: PMC6608035 DOI: 10.1189/jlb.4MR0716-330R
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962