Literature DB >> 15848173

Caspase-3 can be pseudo-activated by a Ca2+-dependent proteolysis at a non-canonical site.

Maude Pelletier1, Lisa Oliver, Khaled Meflah, François M Vallette.   

Abstract

We have shown previously that calcium could trigger nuclear fragmentation, which was associated with a caspase 3 (C3)-like activity [Juin, P., Pelletier, M., Oliver, L., Tremblais, K., Gregoire, M., Meflah, K. and Vallette, F.M. (1998) Induction of a caspase-3-like activity by calcium in normal cytosolic extracts triggers nuclear apoptosis in a cell-free system. J. Biol. Chem. 273, 17559]. Here, we report that this activation is associated with a non-canonical truncation of C3, which induces a weak DEVDase activity. The cleavage of C3 via calcium-dependent proteolysis is independent of caspase 9; lysate exposure to calcium prevents further cleavage and activation by the cytochrome c and dATP pathway. Altogether, our data suggest that calcium could favour a necrotic mechanism by inducing the generation of a form of C3 insensitive to mitochondrial activation.

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Year:  2005        PMID: 15848173     DOI: 10.1016/j.febslet.2005.02.079

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  3 in total

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Authors:  Philana Fernandes; Tracey R O'Donovan; Sharon L McKenna; Patrick F Forde
Journal:  Cancers (Basel)       Date:  2019-08-14       Impact factor: 6.639

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Journal:  Oxid Med Cell Longev       Date:  2013-05-22       Impact factor: 6.543

  3 in total

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