McEnery M W, Dawson T M, Verma A, Gurley D, Colombini M, Snyder S H
Department of Neuroscience, Johns Hopkins Medical Institutions, Baltimore, Maryland 21205.
J Biol Chem. 1993 Nov 5;268(31):23289-96.
The purified mitochondrial benzodiazepine receptor (mBzR) is a complex comprising the voltage-dependent anion channel (VDAC), adenine nucleotide carrier, and an 18-kDa protein that binds isoquinoline carboxamide ligands (McEnery, M. W., Snowman, A. M., Trifiletti, R. R., and Snyder, S. H. (1992) Proc. Natl. Acad. Sci. U.S.A. 89, 3170-3174). An antiserum raised against the mBzR complex reacts selectively with VDAC and is used, along with purification, electrophysiological and immunohistochemical techniques, to characterize the properties and distribution of rat brain VDAC. Although purified VDAC displays biochemical and electrical conductance properties similar to VDAC from other sources, the immunohistochemical distribution of VDAC in rat brain is heterogeneous with pronounced regional variations; the pontine nuclei, the supraoptic nucleus, Purkinje cells of the cerebellum, and the caudate putamen evidence the highest density. The distribution of VDAC is inclusive of the more discretely localized 18-kDa mBzR protein, suggesting that only a portion of the total VDAC participates in the mBzR. The histochemical localizations of the mitochondrial marker enzymes glutamate dehydrogenase and cytochrome c oxidase also indicate marked regional variability in both mitochondrial content and composition. The discrete expression of VDAC reflects a striking heterogeneity of rat brain mitochondria and underlying differences in the utilization of mitochondrial outer membrane ion channels.
纯化的线粒体苯二氮䓬受体(mBzR)是一种复合物,由电压依赖性阴离子通道(VDAC)、腺嘌呤核苷酸载体和一种与异喹啉羧酰胺配体结合的18 kDa蛋白质组成(McEnery, M. W., Snowman, A. M., Trifiletti, R. R., and Snyder, S. H. (1992) Proc. Natl. Acad. Sci. U.S.A. 89, 3170 - 3174)。针对mBzR复合物产生的抗血清与VDAC选择性反应,并与纯化、电生理和免疫组织化学技术一起用于表征大鼠脑VDAC的特性和分布。尽管纯化的VDAC显示出与其他来源的VDAC相似的生化和电导特性,但VDAC在大鼠脑中的免疫组织化学分布是异质性的,具有明显的区域差异;脑桥核、视上核、小脑浦肯野细胞和尾状壳核的密度最高。VDAC的分布包括定位更离散的18 kDa mBzR蛋白,这表明总VDAC中只有一部分参与mBzR。线粒体标记酶谷氨酸脱氢酶和细胞色素c氧化酶的组织化学定位也表明线粒体含量和组成存在明显的区域差异。VDAC的离散表达反映了大鼠脑线粒体的显著异质性以及线粒体外膜离子通道利用的潜在差异。