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Connective tissue growth factor mRNA expression is upregulated in bleomycin-induced lung fibrosis

1  Section of Pulmonary Diseases, Critical Care, and Environmental Medicine, Department of Medicine; 2  Department of Pathology and Environmental Health Sciences; and 3  Tulane/Xavier Center for Bioenvironmental Research, Tulane University Medical Center, New Orleans, Louisiana 70112; and 4  Departa...

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Bibliographic Details
Published in:American journal of physiology. Lung cellular and molecular physiology 1998-08, Vol.275 (2), p.365-L371
Main Authors: Lasky, Joseph A, Ortiz, Luis A, Tonthat, Boihoang, Hoyle, Gary W, Corti, Miriam, Athas, Grace, Lungarella, Giuseppe, Brody, Arnold, Friedman, Mitchell
Format: Article
Language:English
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Summary:1  Section of Pulmonary Diseases, Critical Care, and Environmental Medicine, Department of Medicine; 2  Department of Pathology and Environmental Health Sciences; and 3  Tulane/Xavier Center for Bioenvironmental Research, Tulane University Medical Center, New Orleans, Louisiana 70112; and 4  Departament di Patologia Generale, Universita di Siena, Siena, Italy 53100 Connective tissue growth factor (CTGF) is a newly described 38-kDa peptide mitogen for fibroblasts and a promoter of connective tissue deposition in the skin. The CTGF gene promotor contains a transforming growth factor- 1 (TGF- 1) response element. Because TGF- 1 expression is upregulated in several models of fibroproliferative lung disease, we asked whether CTGF is also upregulated in a murine lung fibrosis model and whether CTGF could mediate some of the fibrogenic effects associated with TGF- 1. A portion of the rat CTGF gene was cloned and used to show that primary isolates of both murine and human lung fibroblasts express CTGF mRNA in vitro. There was a greater than twofold increase in CTGF expression in both human and murine lung fibroblasts 2, 4, and 24 h after the addition of TGF- 1 in vitro. A bleomycin-sensitive mouse strain (C57BL/6) and a bleomycin-resistant mouse strain (BALB/c) were given bleomycin, a known lung fibrogenic agent. CTGF mRNA expression was upregulated in the sensitive, but not in the resistant, mouse strain after administration of bleomycin. In vivo differences in the CTGF expression between the two mouse strains were not due to an inherent inability of BALB/c lung fibroblasts to respond to TGF- 1 because fibroblasts from untreated BALB/c mouse lung upregulated their CTGF message when treated with TGF- 1 in vitro. These data demonstrate that CTGF is expressed in lung fibroblasts and may play a role in the pathogenesis of lung fibrosis. transforming growth factor- 1; collagen; mice
ISSN:1040-0605
1522-1504
DOI:10.1152/ajplung.1998.275.2.l365