| Literature DB >> 33405294 |
Chantal Donovan1,2, Gang Liu1, Sj Shen1, Jacqueline E Marshall1, Richard Y Kim1,2, Charlotte A Alemao2, Kurtis F Budden2, Jaesung P Choi1, Maija Kohonen-Corish3, Emad M El-Omar4, Ian A Yang5, Philip M Hansbro1,2.
Abstract
The nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) family, pyrin domain-containing protein 3 (NLRP3) inflammasome, is one of the most well-characterized inflammasomes, activated by pathogen-associated molecular patterns and damage-associated molecular patterns, including from commensal or pathogenic bacterial and viral infections. The NLRP3 inflammasome promotes inflammatory cell recruitment and regulates immune responses in tissues such as the gastrointestinal tract and the lung, and is involved in many diseases that affect the gut and lung. Recently, the microbiome in the gut and the lung, and the crosstalk between these organs (gut-lung axis), has been identified as a potential mechanism that may influence disease in a bidirectional manner. In this review, we focus on themes presented in this area at the 2019 World Congress on Inflammation. We discuss recent evidence on how the microbiome can affect NLRP3 inflammasome responses in the gut and lung, the role of this inflammasome in regulating gut and lung inflammation in disease, and its potential role in the gut-lung axis. We highlight the exponential increase in our understanding of the NLRP3 inflammasome due to the synthesis of the NLRP3 inflammasome inhibitor, MCC950, and propose future studies that may further elucidate the roles of the NLRP3 inflammasome in gut and lung diseases. ©2020 Society for Leukocyte Biology.Entities:
Keywords: NLRP3 inflammasome; gut; lung; microbiome; microbiota
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Year: 2020 PMID: 33405294 DOI: 10.1002/JLB.3MR0720-472RR
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962