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Am J Physiol Gastrointest Liver Physiol 285: G539-G546, 2003. First published June 4, 2003; doi:10.1152/ajpgi.00436.2002
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HORMONES AND SIGNALING

Transforming growth factor-{beta}1 downregulation of Smad1 gene expression in rat hepatic stellate cells

Hong Shen,1 Guojiang Huang,3 Mohammed Hadi,2 Patrick Choy,2 Manna Zhang,3 Gerald Y. Minuk,3 Yongping Chen,1 and Yuewen Gong1,2,3

1Faculty of Pharmacy and Departments of 2Biochemistry and Medical Genetics and 3Internal Medicine, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada

Submitted 10 October 2002 ; accepted in final form 23 May 2003

Smads are intracellular signaling molecules of the transforming growth factor-{beta} (TGF-{beta}) superfamily that play an important role in the activation of hepatic stellate cells (HSCs) and hepatic fibrosis. Excepting the regulation of Smad7, receptor-regulated Smad gene expression is still unclear. We employed rat HSCs to investigate the expression and regulation of the Smad1 gene, which is a bone morphogenetic protein (BMP) receptor-regulated Smad. We found that the expression and phosphorylation of Smad1 are increased during the activation of HSCs. Moreover, TGF-{beta} significantly inhibits Smad1 gene expression in HSCs in a time- and dose-dependent manner. Furthermore, although both TGF-{beta}1 and BMP2 stimulate the activation of HSCs, they have different effects on HSC proliferation. In conclusion, Smad1 expression and phosphorylation are increased during the activation of HSCs and TGF-{beta}1 significantly inhibits the expression of the Smad1 gene.

transforming growth factor-{beta}; Smad1; regulation



Address for reprint requests and other correspondence: Y. Gong, Faculty of Pharmacy, Univ. of Manitoba, 304-50 Sifton Rd., Winnipeg, MB R3T 2N2 Canada (E-mail: ygong{at}ms.umanitoba.ca).




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