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β-arrestin Deficiency Protects Against Pulmonary Fibrosis in Mice and Prevents Fibroblast Invasion of Extracellular Matrix

Idiopathic pulmonary fibrosis (IPF) is a progressive disease causing unremitting extracellular matrix deposition with resultant distortion of pulmonary architecture and impaired gas exchange. β-arrestins regulate G-protein-coupled receptors through receptor desensitization while acting as signaling...

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Detalhes bibliográficos
Main Authors: Lovgren, Alysia Kern, Kovacs, Jeffrey J., Xie, Ting, Potts, Erin N., Li, Yuejuan, Foster, W. Michael, Liang, Jiurong, Meltzer, Eric B., Jiang, Dianhua, Lefkowitz, Robert J., Noble, Paul W.
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3094726/
https://ncbi.nlm.nih.gov/pubmed/21411739
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/scitranslmed.3001564
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