| Literature DB >> 32433971 |
Supender Kaur1, Alejandro Aballay2.
Abstract
Increasing evidence suggests that deficient immune modulation and microbial infections underline neurodegeneration, but the mechanisms remain obscure. Here, we show that the G-protein-coupled receptor (GPCR) SRBC-48, which belongs to the class BC serpentine receptors, has a protective role in Caenorhabditis elegans dendrite degeneration caused by Pseudomonas aeruginosa infection. Our results indicate that SRBC-48 functions in a cell-autonomous manner in AWC neurons to protect against infection-associated dendrite degeneration. The absence of SRBC-48 results in a reduced lifespan caused by a pathogen infection early in life that induces dendrite degeneration. The decreased longevity in animals deficient in SRBC-48 is due to uncontrolled activation of immune genes, particularly those regulated by the FOXO family transcription factor DAF-16 that is part of the insulin/insulin-like growth factor (IGF)-1 receptor homolog DAF-2. These results reveal how an infection early in life can not only induce dendrite degeneration but also reduce lifespan.Entities:
Keywords: Caenorhabditis elegans; DAF-16; G-protein-coupled receptor; Pseudomonas aeruginosa; SRBC-48; infection; inflammation; longevity; neurodegeneration; pathogens
Mesh:
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Year: 2020 PMID: 32433971 PMCID: PMC7304231 DOI: 10.1016/j.celrep.2020.107662
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423