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Role of chitin and chitinase/chitinase-like proteins in inflammation, tissue remodeling, and injury.
Lee, Chun Geun; Da Silva, Carla A; Dela Cruz, Charles S; Ahangari, Farida; Ma, Bing; Kang, Min-Jong; He, Chuan-Hua; Takyar, Seyedtaghi; Elias, Jack A.
Afiliación
  • Lee CG; Section of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06520-8057, USA.
Annu Rev Physiol ; 73: 479-501, 2011.
Article en En | MEDLINE | ID: mdl-21054166
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Quitina / Quitinasas / Remodelación de las Vías Aéreas (Respiratorias) / Inflamación Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Annu Rev Physiol Año: 2011 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Quitina / Quitinasas / Remodelación de las Vías Aéreas (Respiratorias) / Inflamación Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Annu Rev Physiol Año: 2011 Tipo del documento: Article País de afiliación: Estados Unidos