Department of Neurology, University of Maryland, Baltimore, MD 21201, USA.
Biochem Biophys Res Commun. 2013 Jun 14;435(4):671-7. doi: 10.1016/j.bbrc.2013.05.041. Epub 2013 May 17.
Peroxisome proliferator-activated receptor-gamma co-activator 1α (PGC-1α) and PTEN-induced putative kinase 1 (PINK1) are powerful regulators of mitochondrial function. Here, we report that a previously unrecognized, novel 35 kDa PGC-1α isoform localizes to the mitochondrial inner membrane and matrix in brain as determined by protease protection and carbonate extraction assays, as well as by immunoelectron microscopy. Immunoelectron microscopy and import experiments in vitro revealed that 35 kDa PGC-1α colocalizes and interacts with the voltage-dependent anion channel (VDAC), and that its import depends on VDAC. Valinomycin treatment which depolarizes the membrane potential, abolished mitochondrial localization of the 35 kDa PGC-1α. Using blue native-PAGE, co-immunoprecipitation, and immunoelectron microscopy analyses, we found that the 35 kDa PGC-1α binds and colocalizes with PINK1 in brain mitochondria. This is the first report regarding mitochondrial localization of a novel 35 kDa PGC-1α isoform and its association with PINK1, suggesting possible regulatory roles for mitochondrial function in the brain.
过氧化物酶体增殖物激活受体γ共激活因子 1α(PGC-1α)和 PTEN 诱导的假定激酶 1(PINK1)是线粒体功能的强大调节因子。在这里,我们报告了一种以前未被识别的新型 35 kDa PGC-1α 同工型,其在脑内定位于线粒体内膜和基质,这是通过蛋白酶保护和碳酸盐提取测定、免疫电子显微镜以及免疫电子显微镜和体外导入实验确定的。免疫电子显微镜和体外导入实验表明,35 kDa PGC-1α 与电压依赖性阴离子通道(VDAC)共定位并相互作用,其导入依赖于 VDAC。缬氨霉素处理使膜电位去极化,从而消除了 35 kDa PGC-1α 的线粒体定位。通过蓝 Native-PAGE、共免疫沉淀和免疫电子显微镜分析,我们发现 35 kDa PGC-1α 在脑线粒体中与 PINK1 结合并共定位。这是关于新型 35 kDa PGC-1α 同工型在脑线粒体中的定位及其与 PINK1 结合的首次报道,提示线粒体功能可能对大脑具有调节作用。