Granzyme B-mediated apoptosis proceeds predominantly through a Bcl-2-inhibitable mitochondrial pathway

J Biol Chem. 2001 Apr 13;276(15):12060-7. doi: 10.1074/jbc.M009038200. Epub 2001 Jan 12.

Abstract

Cytotoxic T lymphocytes kill virus-infected and tumor cell targets through the concerted action of proteins contained in cytolytic granules, primarily granzyme B and perforin. Granzyme B, a serine proteinase with substrate specificity similar to the caspase family of apoptotic cysteine proteinases, is capable of cleaving and activating a number of death proteins in target cells. Despite the ability to engage the death pathway at multiple entry points, the preferred mechanism for rapid induction of apoptosis by granzyme B has yet to be clearly established. Here we use time lapse confocal microscopy to demonstrate that mitochondrial cytochrome c release is the primary mode of granzyme B-induced apoptosis and that Bcl-2 is a potent inhibitor of this pivotal event. Caspase activation is not required for cytochrome c release, an activity that correlates with cleavage and activation of Bid, which we have found to be cleaved more readily by granzyme B than either caspase-3 or caspase-8. Bcl-2 blocks the rapid destruction of targets by granzyme B by blocking mitochondrial involvement in the process.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Apoptosis / drug effects*
  • Cytochrome c Group / metabolism
  • Enzyme Activation
  • Granzymes
  • Humans
  • Hydrolysis
  • Jurkat Cells
  • Kinetics
  • Mitochondria / physiology*
  • Molecular Sequence Data
  • Proto-Oncogene Proteins c-bcl-2 / physiology*
  • Serine Endopeptidases / pharmacology*

Substances

  • Cytochrome c Group
  • Proto-Oncogene Proteins c-bcl-2
  • GZMB protein, human
  • Granzymes
  • Serine Endopeptidases