Sánchez del Pino M M, Hawkins R A, Peterson D R
Department of Physiology and Biophysics, Finch University of Health Sciences, Chicago Medical School, Illinois 60064, USA.
J Biol Chem. 1995 Jun 23;270(25):14907-12. doi: 10.1074/jbc.270.25.14907.
Luminal and abluminal membrane vesicles derived from bovine brain endothelial cells, the site of the blood-brain barrier, were fractionated in a discontinuous Ficoll gradient. A mathematical analysis was developed to determine the membrane distribution of membrane marker enzyme activities as well as the ratio of luminal to abluminal membrane in each fraction of the gradient. The results of this analysis indicate that gamma-glutamyl transpeptidase and amino acid transport system A are located on the luminal and abluminal membranes, respectively. Conversely, 5'-nucleotidase and alkaline phosphatase activities are evenly distributed between both membranes. Although Na+/K(+)-ATPase activity is primarily located on the abluminal membrane, approximately 25% of the activity is of luminal origin. Na+/K(+)-ATPase activities associated with each membrane showed different ouabain sensitivities, suggesting that different isoenzymes are located in luminal and abluminal membranes. The analytical procedure used in this study provides a quantitative means to determine the distribution of marker enzymes and transport proteins in partially purified membrane vesicle populations.
源自血脑屏障所在部位牛脑内皮细胞的管腔膜囊泡和管腔外膜囊泡,在不连续的菲可梯度中进行了分级分离。开发了一种数学分析方法,以确定膜标记酶活性的膜分布以及梯度各部分中管腔膜与管腔外膜的比例。该分析结果表明,γ-谷氨酰转肽酶和氨基酸转运系统A分别位于管腔膜和管腔外膜上。相反,5'-核苷酸酶和碱性磷酸酶活性在两种膜之间均匀分布。尽管Na+/K(+)-ATP酶活性主要位于管腔外膜,但约25%的活性来自管腔。与每种膜相关的Na+/K(+)-ATP酶活性表现出不同的哇巴因敏感性,这表明不同的同工酶位于管腔膜和管腔外膜中。本研究中使用的分析程序提供了一种定量方法,以确定标记酶和转运蛋白在部分纯化的膜囊泡群体中的分布。