GRP78 and CHOP modulate macrophage apoptosis and the development of bleomycin-induced pulmonary fibrosis

Author:

Ayaub Ehab A12,Kolb Philipp S1,Mohammed-Ali Zahraa3,Tat Victor1,Murphy James1,Bellaye Pierre-Simon1,Shimbori Chiko1,Boivin Felix J2,Lai Rocky2,Lynn Edward G3ORCID,Lhoták Šárka3,Bridgewater Darren2,Kolb Martin RJ12,Inman Mark D1,Dickhout Jeffrey G3,Austin Richard C3,Ask Kjetil12ORCID

Affiliation:

1. Department of Medicine, Firestone Institute for Respiratory Health; McMaster University and the Research Institute of St. Joe's Hamilton; ON Canada

2. Department of Pathology and Molecular Medicine; McMaster Immunology Research Center, McMaster University; Hamilton ON Canada

3. Department of Medicine, Hamilton Centre for Kidney Research; McMaster University and the Research Institute of St. Joe's Hamilton; ON Canada

Funder

Ontario Thoracic Society

Canadian Institutes of Health Research

Heart and Stroke Foundation of Canada

Publisher

Wiley

Subject

Pathology and Forensic Medicine

Reference72 articles.

1. Idiopathic pulmonary fibrosis;King;Lancet,2011

2. Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy;Selman;Ann Intern Med,2001

3. The myofibroblast in pulmonary fibrosis;Phan;Chest,2002

4. Strategies for anti-fibrotic therapies;Rosenbloom;Biochim Biophys Acta,1832

5. Fibroblasts of granulation tissue: immunofluorescent staining with antismooth muscle serum;Hirschel;Proc Soc Exp Biol Med,1971

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