Wnt signaling enhances the activation and survival of human hepatic stellate cells

  • Sun Jung Myung
  • , Jung Hwan Yoon
  • , Geum Youn Gwak
  • , Won Kim
  • , Jeong Hoon Lee
  • , Kang Mo Kim
  • , Chan Soo Shin
  • , Ja June Jang
  • , Sung Hee Lee
  • , Soo Mi Lee
  • , Hyo Suk Lee

Research output: Contribution to journalArticlepeer-review

Abstract

Wnt signaling was implicated in pulmonary and renal fibrosis. Since Wnt activity is enhanced in liver cirrhosis, Wnt signaling may also participate in hepatic fibrogenesis. Thus, we determined if Wnt signaling modulates hepatic stellate cell (HSC) activation and survival. Wnt3A treatment significantly activated human HSCs, while this was inhibited in secreted frizzled-related protein 1 (sFRP1) overexpressing cells. Wnt3A treatment significantly suppressed TRAIL-induced apoptosis in control HSCs versus sFRP1 over-expressing cells. Particularly, caspase 3 was more activated in sFRP1 over-expressing cells following TRAIL and Wnt3A treatment. These observations imply that Wnt signaling promotes hepatic fibrosis by enhancing HSC activation and survival.

Original languageEnglish
Pages (from-to)2954-2958
Number of pages5
JournalFEBS Letters
Volume581
Issue number16
DOIs
StatePublished - 26 Jun 2007
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Apoptosis
  • Fibrosis
  • Hepatic stellate cell
  • Secreted frizzled-related protein 1
  • Wnt

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