| Literature DB >> 27913791 |
Tanmay Majumdar1, Jayeeta Dhar1, Sonal Patel1, Roman Kondratov1, Sailen Barik1.
Abstract
BMAL1 (brain and muscle ARNT-like protein 1, also known as MOP3 or ARNT3) belongs to the family of the basic helix-loop-helix (bHLH)-PAS domain-containing transcription factors, and is a key component of the molecular oscillator that generates circadian rhythms. Here, we report that BMAL1-deficient cells are significantly more susceptible to infection by two major respiratory viruses of the Paramyxoviridae family, namely RSV and PIV3. Embryonic fibroblasts from Bmal1-/- mice produced nearly 10-fold more progeny virus than their wild type controls. These results were supported by animal studies whereby pulmonary infection of RSV produced a more severe disease and morbidity in Bmal1-/-mice. These results show that BMAL1 can regulate cellular innate immunity against specific RNA viruses.Entities:
Keywords: BMAL1; Paramyxovirus; Toxoplasma gondii; circadian clock; innate immunity; parainfluenza virus; pneumovirus; respiratory syncytial virus
Mesh:
Substances:
Year: 2016 PMID: 27913791 DOI: 10.1177/1753425916681075
Source DB: PubMed Journal: Innate Immun ISSN: 1753-4259 Impact factor: 2.680