| Literature DB >> 21054166 |
Chun Geun Lee1, Carla A Da Silva, Charles S Dela Cruz, Farida Ahangari, Bing Ma, Min-Jong Kang, Chuan-Hua He, Seyedtaghi Takyar, Jack A Elias.
Abstract
The 18 glycosyl hydrolase family of chitinases is an ancient gene family that is widely expressed from prokaryotes to eukaryotes. In mammals, despite the absence of endogenous chitin, a number of chitinases and chitinase-like proteins (C/CLPs) have been identified. However, their roles have only recently begun to be elucidated. Acidic mammalian chitinase (AMCase) inhibits chitin-induced innate inflammation; augments chitin-free, allergen-induced Th2 inflammation; and mediates effector functions of IL-13. The CLPs BRP-39/YKL-40 (also termed chitinase 3-like 1) inhibit oxidant-induced lung injury, augments adaptive Th2 immunity, regulates apoptosis, stimulates alternative macrophage activation, and contributes to fibrosis and wound healing. In accord with these findings, levels of YKL-40 in the lung and serum are increased in asthma and other inflammatory and remodeling disorders and often correlate with disease severity. Our understanding of the roles of C/CLPs in inflammation, tissue remodeling, and tissue injury in health and disease is reviewed below.Entities:
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Year: 2011 PMID: 21054166 PMCID: PMC3864643 DOI: 10.1146/annurev-physiol-012110-142250
Source DB: PubMed Journal: Annu Rev Physiol ISSN: 0066-4278 Impact factor: 19.318