Knockdown of Astrocyte Elevated Gene-1 Inhibits Activation of Hepatic Stellate Cells

Dig Dis Sci. 2016 Jul;61(7):1961-71. doi: 10.1007/s10620-016-4075-8. Epub 2016 Feb 15.

Abstract

Background: Astrocyte elevated gene-1 (AEG-1) is a positive regulator of tumorigenesis and a valuable prognostic marker of a diverse array of cancers, including liver cancer; however, the relationship between AEG-1 and hepatic fibrogenesis is not known.

Objective: The objective of this study was to explore the expression of AEG-1 during hepatic fibrogenesis and determine how AEG-1 regulates the profibrogenic phenotype of hepatic stellate cells (HSCs).

Methods: The levels of AEG-1 were monitored in the fibrotic livers and transforming growth factor-β (TGF-β)- or lipopolysaccharide (LPS)-stimulated HSCs. The expression of AEG-1 was knocked down by lentivirus-mediated short hairpin RNA in HSCs, and collagen expression, proliferation assays, apoptosis induction studies, and migration assays were simultaneously conducted in vitro.

Results: AEG-1 expression was increased in the fibrotic livers. At the cellular level, TGF-β or LPS stimulation, which caused HSC activation, induced AEG-1 expression in HSC-T6 and primary rat HSCs (P < 0.05). Knockdown of AEG-1 inhibited collagen I and α-smooth muscle actin expression (P < 0.05), reduced cell proliferation (P < 0.05) and motility (P < 0.05), and induced cell apoptosis (P < 0.05) in HSCs. This antifibrotic effect caused by lack of AEG-1 was associated with the inactivation of PI3K/Akt and the mitogen-activated protein kinase pathway.

Conclusions: Knockdown of AEG-1 suppressed the activation of HSCs by modulating the phenotype and inducing apoptosis. AEG-1 might be a potential target in treatment of hepatic fibrosis.

Keywords: Activation; Astrocyte elevated gene-1; Hepatic stellate cell; Liver fibrosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Bile Ducts / surgery
  • Cell Cycle
  • Cell Line
  • Cell Proliferation
  • Dimethylnitrosamine / toxicity
  • Gene Expression Regulation / physiology
  • Gene Knockdown Techniques
  • Hepatic Stellate Cells / physiology*
  • Humans
  • Ligation
  • Liver Cirrhosis / chemically induced
  • Liver Cirrhosis / etiology
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Up-Regulation

Substances

  • Dimethylnitrosamine