Cytosolic NADP(+)-dependent isocitrate dehydrogenase regulates cadmium-induced apoptosis

Biochem Pharmacol. 2010 Apr 1;79(7):1072-80. doi: 10.1016/j.bcp.2009.11.014. Epub 2009 Nov 26.


Cadmium ions have a high affinity for thiol groups. Therefore, they may disturb many cellular functions. We recently reported that cytosolic NADP(+)-dependent isocitrate dehydrogenase (IDPc) functions as an antioxidant enzyme to supply NADPH, a major source of reducing equivalents to the cytosol. Cadmium decreased the activity of IDPc both as a purified enzyme and in cultured cells. In the present study, we demonstrate that the knockdown of IDPc expression in HEK293 cells greatly enhances apoptosis induced by cadmium. Transfection of HEK293 cells with an IDPc small interfering RNA significantly decreased the activity of IDPc and enhanced cellular susceptibility to cadmium-induced apoptosis as indicated by the morphological evidence of apoptosis, DNA fragmentation and condensation, cellular redox status, mitochondria redox status and function, and the modulation of apoptotic marker proteins. Taken together, our results suggest that suppressing the expression of IDPc enhances cadmium-induced apoptosis of HEK293 cells by increasing disruption of the cellular redox status.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Cadmium / pharmacology*
  • Caspase 3 / physiology
  • Cells, Cultured
  • Cytosol / enzymology*
  • Humans
  • Isocitrate Dehydrogenase / antagonists & inhibitors
  • Isocitrate Dehydrogenase / physiology*
  • Mitochondria / drug effects
  • NADP / metabolism*
  • Oxidation-Reduction
  • RNA, Small Interfering / genetics


  • RNA, Small Interfering
  • Cadmium
  • NADP
  • Isocitrate Dehydrogenase
  • Caspase 3