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

被引:229
作者
Lasky, JA
Ortiz, LA
Tonthat, B
Hoyle, GW
Corti, M
Athas, G
Lungarella, G
Brody, A
Friedman, M
机构
[1] Tulane Univ, Med Ctr, Dept Med, Sect Pulm Dis Crit Care & Environm Med, New Orleans, LA 70112 USA
[2] Tulane Univ, Med Ctr, Dept Pathol & Environm Hlth Sci, New Orleans, LA 70112 USA
[3] Tulane Univ, Med Ctr, Tulane Xavier Ctr Bioenvironm Res, New Orleans, LA 70112 USA
[4] Univ Siena, Dept Patol Gen, I-53100 Siena, Italy
关键词
transforming growth factor-beta 1; collagen; mice;
D O I
10.1152/ajplung.1998.275.2.L365
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
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-beta 1 (TGF-beta 1) response element. Because TGF-beta 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-beta 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-beta 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-beta 1 because fibroblasts from untreated BALB/c mouse lung upregulated their CTGF message when treated with TGF-beta 1 in vitro. These data demonstrate that CTGF is expressed in lung fibroblasts and may play a role in the pathogenesis of lung fibrosis.
引用
收藏
页码:L365 / L371
页数:7
相关论文
共 26 条
[1]  
Baecher-Allan Clare M., 1993, Regional Immunology, V5, P207
[2]   TGF-BETA INDUCES BIMODAL PROLIFERATION OF CONNECTIVE-TISSUE CELLS VIA COMPLEX CONTROL OF AN AUTOCRINE PDGF LOOP [J].
BATTEGAY, EJ ;
RAINES, EW ;
SEIFERT, RA ;
BOWENPOPE, DF ;
ROSS, R .
CELL, 1990, 63 (03) :515-524
[3]  
BAUMAN MD, 1990, EUR J CELL BIOL, V51, P327
[4]   CONNECTIVE-TISSUE GROWTH-FACTOR - A CYSTEINE-RICH MITOGEN SECRETED BY HUMAN VASCULAR ENDOTHELIAL-CELLS IS RELATED TO THE SRC-INDUCED IMMEDIATE EARLY GENE-PRODUCT CEF-10 [J].
BRADHAM, DM ;
IGARASHI, A ;
POTTER, RL ;
GROTENDORST, GR .
JOURNAL OF CELL BIOLOGY, 1991, 114 (06) :1285-1294
[5]   CYTOKINE NETWORKS IN THE REGULATION OF INFLAMMATION AND FIBROSIS IN THE LUNG [J].
ELIAS, JA ;
FREUNDLICH, B ;
KERN, JA ;
ROSENBLOOM, J .
CHEST, 1990, 97 (06) :1439-1445
[6]   MURINE STRAIN DIFFERENCES IN PULMONARY BLEOMYCIN METABOLISM [J].
FILDERMAN, AE ;
LAZO, JS .
BIOCHEMICAL PHARMACOLOGY, 1991, 42 (01) :195-198
[7]   Stimulation of fibroblast cell growth, matrix production, and granulation tissue formation by connective tissue growth factor [J].
Frazier, K ;
Williams, S ;
Kothapalli, D ;
Klapper, H ;
Grotendorst, GR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (03) :404-411
[8]  
Grotendorst GR, 1996, CELL GROWTH DIFFER, V7, P469
[9]   MURINE STRAIN DIFFERENCES IN ACUTE LUNG INJURY AND ACTIVATION OF POLY(ADP-RIBOSE) POLYMERASE BY IN-VITRO EXPOSURE OF LUNG SLICES TO BLEOMYCIN [J].
HOYT, DG ;
LAZO, JS .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 7 (06) :645-651
[10]   SIGNIFICANT CORRELATION BETWEEN CONNECTIVE-TISSUE GROWTH-FACTOR GENE-EXPRESSION AND SKIN SCLEROSIS IN TISSUE-SECTIONS FROM PATIENTS WITH SYSTEMIC-SCLEROSIS [J].
IGARASHI, A ;
NASHIRO, K ;
KIKUCHI, K ;
SATO, S ;
IHN, H ;
GROTENDORST, GR ;
TAKEHARA, K .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 105 (02) :280-284