Literature DB >> 29576451

IRF8 Regulates Transcription of Naips for NLRC4 Inflammasome Activation.

Rajendra Karki1, Ein Lee2, David Place1, Parimal Samir1, Jayadev Mavuluri1, Bhesh Raj Sharma1, Arjun Balakrishnan1, R K Subbarao Malireddi1, Rechel Geiger1, Qifan Zhu2, Geoffrey Neale3, Thirumala-Devi Kanneganti4.   

Abstract

Inflammasome activation is critical for host defenses against various microbial infections. Activation of the NLRC4 inflammasome requires detection of flagellin or type III secretion system (T3SS) components by NLR family apoptosis inhibitory proteins (NAIPs); yet how this pathway is regulated is unknown. Here, we found that interferon regulatory factor 8 (IRF8) is required for optimal activation of the NLRC4 inflammasome in bone-marrow-derived macrophages infected with Salmonella Typhimurium, Burkholderia thailandensis, or Pseudomonas aeruginosa but is dispensable for activation of the canonical and non-canonical NLRP3, AIM2, and Pyrin inflammasomes. IRF8 governs the transcription of Naips to allow detection of flagellin or T3SS proteins to mediate NLRC4 inflammasome activation. Furthermore, we found that IRF8 confers protection against bacterial infection in vivo, owing to its role in inflammasome-dependent cytokine production and pyroptosis. Altogether, our findings suggest that IRF8 is a critical regulator of NAIPs and NLRC4 inflammasome activation for defense against bacterial infection.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Burkholderia; ICSBP; IRF8; NAIP; NLR; NLRC4; PU.1; Salmonella; caspase-1; inflammasome

Mesh:

Substances:

Year:  2018        PMID: 29576451      PMCID: PMC5935577          DOI: 10.1016/j.cell.2018.02.055

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


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