Activin A-Smad Signaling Mediates Connective Tissue Growth Factor Synthesis in Liver Progenitor Cells

Int J Mol Sci. 2016 Mar 22;17(3):408. doi: 10.3390/ijms17030408.

Abstract

Liver progenitor cells (LPCs) are activated in chronic liver damage and may contribute to liver fibrosis. Our previous investigation reported that LPCs produced connective tissue growth factor (CTGF/CCN2), an inducer of liver fibrosis, yet the regulatory mechanism of the production of CTGF/CCN2 in LPCs remains elusive. In this study, we report that Activin A is an inducer of CTGF/CCN2 in LPCs. Here we show that expression of both Activin A and CTGF/CCN2 were upregulated in the cirrhotic liver, and the expression of Activin A positively correlates with that of CTGF/CCN2 in liver tissues. We go on to show that Activin A induced de novo synthesis of CTGF/CCN2 in LPC cell lines LE/6 and WB-F344. Furthermore, Activin A contributed to autonomous production of CTGF/CCN2 in liver progenitor cells (LPCs) via activation of the Smad signaling pathway. Smad2, 3 and 4 were all required for this induction. Collectively, these results provide evidence for the fibrotic role of LPCs in the liver and suggest that the Activin A-Smad-CTGF/CCN2 signaling in LPCs may be a therapeutic target of liver fibrosis.

Keywords: Activin A; Smad proteins; connective tissue growth factor; liver fibrosis; oval cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activins / genetics
  • Activins / metabolism*
  • Adult Stem Cells / metabolism*
  • Animals
  • Case-Control Studies
  • Connective Tissue Growth Factor / genetics
  • Connective Tissue Growth Factor / metabolism*
  • HEK293 Cells
  • Humans
  • Liver Cirrhosis / metabolism*
  • Liver Cirrhosis / pathology
  • Rats
  • Signal Transduction
  • Smad Proteins / metabolism*
  • Up-Regulation

Substances

  • CCN2 protein, human
  • Smad Proteins
  • activin A
  • Activins
  • Connective Tissue Growth Factor