Degradation of Mcl-1 by granzyme B: implications for Bim-mediated mitochondrial apoptotic events

J Biol Chem. 2004 May 21;279(21):22020-9. doi: 10.1074/jbc.M313234200. Epub 2004 Mar 10.

Abstract

Recent studies have suggested that in the absence of Bid, granzyme B (GrB) can utilize an unknown alternative pathway to mediate mitochondrial apoptotic events. The current study has elucidated just such a pathway for GrB-mediated mitochondrial apoptotic alterations. Two Bcl-2 family members have been identified as interactive players in this newly discovered mitochondrial response to GrB: the pro-survival protein Mcl-1L and the pro-apoptotic protein, Bim. Expression of Mcl-1L, which localizes mainly to the outer mitochondrial membrane, decreases significantly in cells subjected to CTL-free cytotoxicity mediated by a combination of GrB and replication-deficient adenovirus. The data suggest that Mcl-1L is a substrate for GrB and for caspase-3, but the two enzymes appear to target different cleavage sites. The cleavage pattern of endogenous Mcl-1L resembles that of in vitro translated Mcl-1L subjected to similar proteolytic activity. Co-immunoprecipitation experiments performed with endogenous as well as with in vitro translated proteins suggest that Mcl-1L is a high affinity binding partner of the three isoforms of Bim (extra-long, long, and short). Bim, a BH3-only protein, is capable of mediating the release of mitochondrial cytochrome c, and this activity is inhibited by the presence of exogenous Mcl-1L. The findings presented herein imply that Mcl-1L degradation by either GrB or caspase-3 interferes with Bim sequestration by Mcl-1L.

Publication types

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

MeSH terms

  • Adenoviridae / genetics
  • Animals
  • Apoptosis Regulatory Proteins
  • Apoptosis*
  • Bcl-2-Like Protein 11
  • Binding Sites
  • Blotting, Western
  • Carrier Proteins / metabolism*
  • Caspase 3
  • Caspases / metabolism
  • Cell Survival
  • Cloning, Molecular
  • Cytochromes c / metabolism
  • Down-Regulation
  • Electrophoresis, Polyacrylamide Gel
  • Granzymes
  • HeLa Cells
  • Humans
  • Jurkat Cells
  • Membrane Proteins / metabolism*
  • Mice
  • Mitochondria / metabolism
  • Mitochondria / pathology*
  • Myeloid Cell Leukemia Sequence 1 Protein
  • Neoplasm Proteins / metabolism*
  • Precipitin Tests
  • Protein Binding
  • Protein Biosynthesis
  • Protein Isoforms
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-bcl-2*
  • Serine Endopeptidases / pharmacology*
  • Subcellular Fractions
  • Transcription, Genetic

Substances

  • Apoptosis Regulatory Proteins
  • BCL2L11 protein, human
  • Bcl-2-Like Protein 11
  • Bcl2l11 protein, mouse
  • Carrier Proteins
  • Mcl1 protein, mouse
  • Membrane Proteins
  • Myeloid Cell Leukemia Sequence 1 Protein
  • Neoplasm Proteins
  • Protein Isoforms
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Cytochromes c
  • GZMB protein, human
  • Granzymes
  • Gzmb protein, mouse
  • Serine Endopeptidases
  • CASP3 protein, human
  • Casp3 protein, mouse
  • Caspase 3
  • Caspases