Differential protective effects of Bcl-xL and Bcl-2 on apoptotic liver injury in transgenic mice

Am J Physiol. 1999 Sep;277(3):G702-8. doi: 10.1152/ajpgi.1999.277.3.G702.

Abstract

Fas ligand (CD95L) and tumor necrosis factor-alpha (TNF-alpha) are pivotal inducers of hepatocyte apoptosis. Uncontrolled activation of these two systems is involved in several forms of liver injury. Although the broad antiapoptotic action of Bcl-2 and Bcl-xL has been clearly established in various apoptotic pathways, their ability to inhibit the Fas/CD95- and TNF-alpha-mediated apoptotic signal has remained controversial. We have demonstrated that the expression of BCL-2 in hepatocytes protects them against Fas-induced fulminant hepatitis in transgenic mice. The present study shows that transgenic mice overexpressing BCL-XL in hepatocytes are also protected from Fas-induced apoptosis in a dose-dependent manner. Bcl-xL and Bcl-2 were protective without any change in the level of endogenous Bcl-xL or Bax and inhibited hepatic caspase-3-like activity. In vivo injection of TNF-alpha caused massive apoptosis and death only when transcription was inhibited. Under these conditions, PK-BCL-XL mice were partially protected from liver injury and death but PK-BCL-2 mice were not. A similar differential protective effect of Bcl-xL and Bcl-2 transgenes was observed when Fas/CD95 was activated and transcription blocked. These results suggest that apoptosis triggered by activation of both Fas/CD95 and TNF-alpha receptors is to some extent counteracted by the transcription-dependent protective effects, which are essential for the antiapoptotic activity of Bcl-2 but not of Bcl-xL. Therefore, Bcl-xL and Bcl-2 appear to have different antiapoptotic effects in the liver whose characterization could facilitate their use to prevent the uncontrolled apoptosis of hepatocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Caspase 3
  • Caspase Inhibitors
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism
  • Liver / physiology
  • Mice
  • Mice, Inbred Strains
  • Mice, Transgenic / genetics
  • NF-kappa B / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / pharmacology*
  • Pyruvate Kinase / genetics
  • Tumor Necrosis Factor-alpha / pharmacology
  • bcl-X Protein
  • fas Receptor / pharmacology
  • fas Receptor / physiology

Substances

  • BCL2L1 protein, human
  • Bcl2l1 protein, mouse
  • Caspase Inhibitors
  • Enzyme Inhibitors
  • NF-kappa B
  • Proto-Oncogene Proteins c-bcl-2
  • Tumor Necrosis Factor-alpha
  • bcl-X Protein
  • fas Receptor
  • Pyruvate Kinase
  • CASP3 protein, human
  • Casp3 protein, mouse
  • Caspase 3