Human alphaA- and alphaB-crystallins bind to Bax and Bcl-X(S) to sequester their translocation during staurosporine-induced apoptosis

Cell Death Differ. 2004 May;11(5):512-26. doi: 10.1038/sj.cdd.4401384.

Abstract

AlphaA- and alphaB-crystallins are distinct antiapoptotic regulators. Regarding the antiapoptotic mechanisms, we have recently demonstrated that alphaB-crystallin interacts with the procaspase-3 and partially processed procaspase-3 to repress caspase-3 activation. Here, we demonstrate that human alphaA- and alphaB-crystallins prevent staurosporine-induced apoptosis through interactions with members of the Bcl-2 family. Using GST pulldown assays and coimmunoprecipitations, we demonstrated that alpha-crystallins bind to Bax and Bcl-X(S) both in vitro and in vivo. Human alphaA- and alphaB-crystallins display similar affinity to both proapoptotic regulators, and so are true with their antiapoptotic ability tested in human lens epithelial cells, human retina pigment epithelial cells (ARPE-19) and rat embryonic myocardium cells (H9c2) under treatment of staurosporine, etoposide or sorbitol. Two prominent mutants, R116C in alphaA-crystallin and R120G, in alphaB-crystallin display much weaker affinity to Bax and Bcl-X(S). Through the interaction, alpha-crystallins prevent the translocation of Bax and Bcl-X(S) from cytosol into mitochondria during staurosporine-induced apoptosis. As a result, alpha-crystallins preserve the integrity of mitochondria, restrict release of cytochrome c, repress activation of caspase-3 and block degradation of PARP. Thus, our results demonstrate a novel antiapoptotic mechanism for alpha-crystallins.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Caspases / metabolism
  • Cells, Cultured
  • Cytochromes c / metabolism
  • Cytosol / metabolism
  • Epithelial Cells / metabolism
  • Etoposide / toxicity
  • Genes, bcl-2 / physiology
  • Humans
  • Mitochondria / metabolism
  • Mutation / genetics
  • Myocytes, Cardiac / metabolism
  • Protein Transport / physiology
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Rats
  • Sorbitol / toxicity
  • Staurosporine / toxicity
  • alpha-Crystallin A Chain / metabolism*
  • alpha-Crystallin B Chain / metabolism*
  • bcl-2-Associated X Protein
  • bcl-X Protein

Substances

  • BAX protein, human
  • BCL2L1 protein, human
  • Bax protein, rat
  • Bcl2l1 protein, rat
  • Proto-Oncogene Proteins c-bcl-2
  • alpha-Crystallin A Chain
  • alpha-Crystallin B Chain
  • bcl-2-Associated X Protein
  • bcl-X Protein
  • Sorbitol
  • Etoposide
  • Cytochromes c
  • Caspases
  • Staurosporine