Hancock 2016 Amino Acids: Difference between revisions

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|organism=Mouse
|organism=Mouse
|tissues=Liver
|tissues=Liver
|preparations=Intact cells, Isolated mitochondria
|preparations=Intact cells, Isolated mitochondria, Oxidase;biochemical oxidation
|couplingstates=LEAK, ROUTINE, ET
|couplingstates=LEAK, ROUTINE, ET
|pathways=S, Other combinations, ROX
|pathways=S, Other combinations, ROX
}}
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::::* [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969956/ Erratum] to: Co-regulation of mitochondrial respiration by proline dehydrogenase/oxidase and succinate
::::* [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969956/ Erratum] to: Co-regulation of mitochondrial respiration by proline dehydrogenase/oxidase and succinate

Latest revision as of 13:29, 19 February 2019

Publications in the MiPMap
Hancock CN, Liu W, Alvord WG, Phang JM (2016) Co-regulation of mitochondrial respiration by proline dehydrogenase/oxidase and succinate. Amino Acids 48:859-72.

ยป PMID: 26660760 Open Access

Hancock CN, Liu W, Alvord WG, Phang JM (2016) Amino Acids

Abstract: Proline dehydrogenase/oxidase (PRODH/POX) is a mitochondrial protein critical to multiple stress pathways. Because of the roles of PRODH/POX in signaling, and its shared localization to the mitochondrial inner membrane with the electron transport chain (ETC), we investigated whether there was a direct relationship between PRODH/POX and regulation of the ETC. We found that PRODH/POX binds directly to CoQ1 and that CoQ1-dependent PRODH/POX activity required functional Complex III and Complex IV. PRODH/POX supported respiration in living cells during nutrient stress; however, expression of PRODH/POX resulted in an overall decrease in respiratory fitness. Effects on respiratory fitness were inhibited by DHP and NAC, indicating that these effects were mediated by PRODH/POX-dependent reactive oxygen species (ROS) generation. PRODH/POX expression resulted in a dose-dependent down-regulation of Complexes I-IV of the ETC, and this effect was also mitigated by the addition of DHP and NAC. We found that succinate was an uncompetitive inhibitor of PRODH/POX activity, inhibited ROS generation by PRODH/POX, and alleviated PRODH/POX effects on respiratory fitness. The findings demonstrate novel cross-talk between proline and succinate respiration in vivo and provide mechanistic insights into observations from previous animal studies. Our results suggest a potential regulatory loop between PRODH/POX and succinate in regulation of mitochondrial respiration. โ€ข Keywords: Proline โ€ข Bioblast editor: Gnaiger E


Labels: MiParea: Respiration 


Organism: Mouse  Tissue;cell: Liver  Preparation: Intact cells, Isolated mitochondria, Oxidase;biochemical oxidation 


Coupling state: LEAK, ROUTINE, ET  Pathway: S, Other combinations, ROX 



  • Erratum to: Co-regulation of mitochondrial respiration by proline dehydrogenase/oxidase and succinate
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