First Author | Gong J | Year | 2012 |
Journal | FASEB J | Volume | 26 |
Issue | 8 | Pages | 3537-49 |
PubMed ID | 22573912 | Mgi Jnum | J:187462 |
Mgi Id | MGI:5437164 | Doi | 10.1096/fj.11-197376 |
Citation | Gong J, et al. (2012) Two protein kinase C isoforms, delta and epsilon, regulate energy homeostasis in mitochondria by transmitting opposing signals to the pyruvate dehydrogenase complex. FASEB J 26(8):3537-49 |
abstractText | Energy production in mitochondria is a multistep process that requires coordination of several subsystems. While reversible phosphorylation is emerging as the principal tool, it is still unclear how this signal network senses the workloads of processes as different as fuel procurement, catabolism in the Krebs cycle, and stepwise oxidation of reducing equivalents in the electron transfer chain. We previously proposed that mitochondria use oxidized cytochrome c in concert with retinol to activate protein kinase Cdelta, thereby linking a prominent kinase network to the redox balance of the ETC. Here, we show that activation of PKCepsilon in mitochondria also requires retinol as a cofactor, implying a redox-mechanism. Whereas activated PKCdelta transmits a stimulatory signal to the pyruvate dehdyrogenase complex (PDHC), PKCepsilon opposes this signal and inhibits the PDHC. Our results suggest that the balance between PKCdelta and epsilon is of paramount importance not only for flux of fuel entering the Krebs cycle but for overall energy homeostasis. We observed that the synthetic retinoid fenretinide substituted for the retinol cofactor function but, on chronic use, distorted this signal balance, leading to predominance of PKCepsilon over PKCdelta. The suppression of the PDHC might explain the proapoptotic effect of fenretinide on tumor cells, as well as the diminished adiposity observed in experimental animals and humans. Furthermore, a disturbed balance between PKCdelta and PKCepsilon might underlie the injury inflicted on the ischemic myocardium during reperfusion. dehydrogenase complex. |