Regulation of brefeldin A-induced ER stress and apoptosis by mitochondrial NADP⁺-dependent isocitrate dehydrogenase

Biochem Biophys Res Commun. 2012 Jan 13;417(2):760-4. doi: 10.1016/j.bbrc.2011.12.030. Epub 2011 Dec 16.

Abstract

Brefeldin A (BFA), an endoplasmic reticulum (ER)-Golgi transport inhibitor, has been shown to cause accumulation of proteins in the ER, ER stress, and ultimately apoptosis. In this paper, we demonstrate that the knockdown of mitochondrial NADP(+)-dependent isocitrate dehydrogenase (IDPm), a mitochondrial NADPH-generating enzyme, by small interfering RNA (siRNA) enhanced BFA-induced apoptosis. However, attenuated IDPm activity results in the suppression of ER stress response, presumably, via the inhibition of the PI3K/Akt pathway. Collectively, our data suggest that the association of IDPm expression and ER stress confers a survival mechanism in A549 cells against BFA-induced apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology*
  • Apoptosis / drug effects*
  • Brefeldin A / pharmacology*
  • Cell Line, Tumor
  • Endoplasmic Reticulum Stress / drug effects*
  • Isocitrate Dehydrogenase / genetics
  • Isocitrate Dehydrogenase / metabolism*
  • Mitochondria / enzymology*
  • RNA, Small Interfering / genetics
  • Reactive Oxygen Species / metabolism

Substances

  • Anti-Bacterial Agents
  • RNA, Small Interfering
  • Reactive Oxygen Species
  • Brefeldin A
  • Isocitrate Dehydrogenase
  • isocitrate dehydrogenase (NADP+)