Lemeshko Victor V
Escuela de Física, Facultad de Ciencias, Universidad Nacional de Colombia, sede Medellín, Calle 59A, No 63-20, Medellín, Colombia.
Biochim Biophys Acta. 2016 Jul;1858(7 Pt A):1411-8. doi: 10.1016/j.bbamem.2016.04.005. Epub 2016 Apr 13.
Mitochondrial energy in cardiac cells has been reported to be channeled into the cytosol through the intermembrane contact sites formed by the adenine nucleotide translocator, creatine kinase and VDAC. Computational analysis performed in this study showed a high probability of the outer membrane potential (OMP) generation coupled to such a mechanism of energy channeling in respiring mitochondria. OMPs, positive inside, calculated at elevated concentrations of creatine are high enough to restrict ATP release from mitochondria, to significantly decrease the apparent K(m,ADP) for state 3 respiration and to maintain low concentrations of Ca(2+) in the mitochondrial intermembrane space. An inhibition by creatine of Ca(2+)-induced swelling of isolated mitochondria and other protective effects of creatine reported in the literature might be explained by generated positive OMP. We suggest that VDAC-creatine kinase-dependent generation of OMP represents a novel physiological factor controlling metabolic state of mitochondria, cell energy channeling and resistance to death.
据报道,心肌细胞中的线粒体能量通过腺嘌呤核苷酸转位酶、肌酸激酶和电压依赖性阴离子通道(VDAC)形成的膜间接触位点进入细胞质。本研究进行的计算分析表明,呼吸线粒体中与这种能量通道机制相关的外膜电位(OMP)产生的可能性很高。在肌酸浓度升高时计算得出的内部为正的OMP足以限制ATP从线粒体释放,显著降低状态3呼吸的表观K(m,ADP),并维持线粒体膜间空间中低浓度的Ca(2+)。文献中报道的肌酸对分离线粒体Ca(2+)诱导肿胀的抑制作用以及肌酸的其他保护作用可能由产生的正OMP来解释。我们认为,VDAC-肌酸激酶依赖性OMP的产生代表了一种控制线粒体代谢状态、细胞能量通道和抗死亡能力的新的生理因素。