Intracellular calcium release is required for caspase-3 and -9 activation

Cell Biochem Funct. 2004 Jan-Feb;22(1):35-40. doi: 10.1002/cbf.1050.

Abstract

Increase in intracellular Ca2+ [Ca2+]i regulates many biological functions including apoptosis, but the protein(s) linking [Ca2+]i and apoptosis are not completely understood. We have previously shown that IP3R-deficient cells are resistant to T-cell receptor (TCR)-induced apoptosis due to lack of Ca2+ release from endoplasmic reticulum (ER) and calcineurin activation. Here we show that caspase-9 and -3 are not activated in IP3R-deficient cells after TCR stimulation, consistent with the resistance of these cells to apoptosis. However, we also demonstrate that Bcl-2 expression in IP3R-deficient cells is comparable to control cells. Taken together, these results strongly suggest that IP3R-mediated Ca2+ release plays a critical role in regulating the activity of caspases-3 and -9 independent of Bcl-2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Blotting, Western
  • Calcium / metabolism*
  • Calcium Channels / chemistry
  • Calcium Signaling*
  • Caspase 3
  • Caspase 9
  • Caspases / chemistry
  • Caspases / metabolism*
  • Enzyme Activation
  • Humans
  • Inositol 1,4,5-Trisphosphate Receptors
  • Jurkat Cells
  • Proto-Oncogene Proteins c-bcl-2 / chemistry
  • Receptors, Antigen, T-Cell / chemistry
  • Receptors, Cytoplasmic and Nuclear / chemistry

Substances

  • Calcium Channels
  • ITPR1 protein, human
  • Inositol 1,4,5-Trisphosphate Receptors
  • Proto-Oncogene Proteins c-bcl-2
  • Receptors, Antigen, T-Cell
  • Receptors, Cytoplasmic and Nuclear
  • CASP3 protein, human
  • CASP9 protein, human
  • Caspase 3
  • Caspase 9
  • Caspases
  • Calcium