| Literature DB >> 26825124 |
Alexander Czachor1, Athena Failla1, Richard Lockey1, Narasaiah Kolliputi2.
Abstract
In this Perspective, we discuss some recent developments in the study of the mitochondrial scaffolding protein AKAP121 (also known as AKAP1, or AKAP149 as the human homolog), with an emphasis on its role in mitochondrial physiology. AKAP121 has been identified to function as a key regulatory molecule in several mitochondrial events including oxidative phosphorylation, the control of membrane potential, fission-induced apoptosis, maintenance of mitochondrial Ca(2+)homeostasis, and the phosphorylation of various mitochondrial respiratory chain substrate molecules. Furthermore, we discuss the role of hypoxia in prompting cellular stress and damage, which has been demonstrated to mediate the proteosomal degradation of AKAP121, leading to an increase in reactive oxgyen species production, mitochondrial dysfunction, and ultimately cell death.Entities:
Keywords: AKAP1; AKAP121; apoptosis; dysfunction; mitochondria
Mesh:
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Year: 2016 PMID: 26825124 PMCID: PMC4835917 DOI: 10.1152/ajpcell.00292.2015
Source DB: PubMed Journal: Am J Physiol Cell Physiol ISSN: 0363-6143 Impact factor: 4.249