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Effect of Growth Factors on Collagen Metabolism in Cultured Human Heart Fibroblasts

1991; Taylor & Francis; Volume: 26; Issue: 4 Linguagem: Inglês

10.3109/03008209109152444

1607-8438

Chu Chang Chua, Balvin H.L. Chua, Z. Y. Zhao, Christopher J. Krebs, Clement A. Diglio, Eugene V. Perrin,

Protease and Inhibitor Mechanisms

AbstractUsing human heart fibroblasts (HHF), we studied the effect of basic fibroblast growth factor (bFGF) and transforming growth factor-β (TGF-β) on the gene expression of type I collagen, collagenase and tissue inhibitor of metalloproteinases (TIMP). Initially, treatment of HHF with bFGF alone (10 ng/ml) resulted in elevated secretion of collagenase into the culture medium. Subsequent treatment of HHF with TGF-β in combination with bFGF suppressed collagenase secretion. Northern blot analysis reinforced this observation by revealing an enhancement of the steady-state mRNA level of collagenase in response to bFGE In order to examine if the collagenase gene was affected by bFGF at the transcriptional level, transfection experiments were carried out with a plasmid containing collagenase promoter linked to chloramphenicol acetyltransferase gene (CAT). Basic FGF stimulated CAT activity by four-fold, indicating increased promoter activity whereas the combination of TGF-β and bFGF resulted in decreased CAT activity. TGF-β was shown to increase type I collagen and TIMP mRNA levels by 2.5- and 2.1-fold, respectively. These results suggest that TGF-β and bFGF may play a pivotal role in regulating collagen metabolism in HHFKey Words: basic FGFTGF-βcollagenasetissue inhibitor of metalloproteinaseshuman heart fibroblasts