Apoptosis induction resulting from proteasome inhibition

Biochem J. 1996 Jul 15;317 ( Pt 2)(Pt 2):385-8. doi: 10.1042/bj3170385.

Abstract

Proteases are known to be involved in the apoptotic pathway. We report here that benzyloxycarbonyl (Z)-Leu-Leu-leucinal(ZLLLal), a leupeptin analogue, can induce apoptosis in MOLT-4 and L5178Y cells. ZLLLal is a cell-permeant inhibitor of proteasome. Among the protease inhibitors tested, only calpain inhibitor I (acetyl-Leu-Leu-norleucinal) and ZLLLal caused a marked induction of apoptosis in MOLT-4 cells. In contrast Z-Leu-leucinal, a specific inhibitor of calpain, did not induce apoptosis. When MOLT-4 cells were incubated in the presence of ZLLLal, p53 accumulated in the cells. These results strongly suggest that inhibition of proteasome induces p53-dependent apoptosis and that proteasome can protect cell from apoptosis.

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Apoptosis / radiation effects
  • Cysteine Endopeptidases / drug effects*
  • Cysteine Proteinase Inhibitors / pharmacology*
  • Dose-Response Relationship, Drug
  • Humans
  • Leupeptins / pharmacology*
  • Mice
  • Multienzyme Complexes / drug effects*
  • Proteasome Endopeptidase Complex
  • Tumor Cells, Cultured
  • Tumor Suppressor Protein p53 / analysis
  • X-Rays

Substances

  • Cysteine Proteinase Inhibitors
  • Leupeptins
  • Multienzyme Complexes
  • Tumor Suppressor Protein p53
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex
  • benzyloxycarbonylleucyl-leucyl-leucine aldehyde