15
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Smac/DIABLO is not released from mitochondria during apoptotic signalling in cells deficient in cytochrome c.

      Cell Death and Differentiation
      Animals, Apoptosis, drug effects, physiology, Blotting, Western, Caspases, metabolism, Cell Line, Tumor, Cytochromes c, deficiency, Cytosol, Humans, Immunohistochemistry, Intracellular Signaling Peptides and Proteins, analysis, secretion, Mice, Microscopy, Confocal, Mitochondria, Mitochondrial Proteins, NIH 3T3 Cells, Signal Transduction, Staurosporine, pharmacology, bcl-2-Associated X Protein

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          We have characterised the apoptotic defects in cells null for cytochrome c (cyt c-/-). Such cells treated with staurosporine (STS) exhibited translocation to the mitochondria and activation of the proapoptotic signalling molecule Bax but failed to release Smac/DIABLO from these organelles, judged by both confocal microscopy and Western blotting. While reference cells expressing cytochrome c released both it and Smac/DIABLO under a variety of conditions of apoptotic induction, we have never observed release of Smac/DIABLO from cyt c-/- cells. We eliminate the possibility that proteasomal degradation of cytosolically localised Smac/DIABLO is responsible for our failure to visualise the protein outside the mitochondria. Our findings indicate an unanticipated nexus between release of cytochrome c and Smac/DIABLO from mitochondria, previously thought to be a more or less synchronised event early in apoptosis. We suggest that the failure of cyt c-/- cells to release Smac/DIABLO after recruitment of Bax to mitochondria represents an extreme manifestation of some inherent difference in the regulation of release of these two proteins from mitochondria.

          Related collections

          Author and article information

          Comments

          Comment on this article