O'Donnell M E, Martinez A, Sun D
Department of Human Physiology, School of Medicine, University of California, Davis 95616.
Am J Physiol. 1995 Mar;268(3 Pt 1):C747-54. doi: 10.1152/ajpcell.1995.268.3.C747.
Brain microvascular endothelial cells play an important role in regulation of ion and fluid movement between the blood and the brain interstitium. Astrocytes have been shown to induce blood-brain barrier properties in the endothelial cells, including formation of tight junctions and increased expression and asymmetric distribution of enzymes and ion transport systems. Previous studies have demonstrated that endothelial cells of bovine aorta possess a highly active Na-K-Cl cotransport system that participates in intracellular volume regulation. The present study was conducted to evaluate Na-K-Cl cotransport activity of cerebral microvascular endothelial cells and to determine whether astrocyte-conditioned medium (CM) influences Na-K-Cl cotransport activity of these cells. We found the brain microvascular endothelial cells to exhibit a robust Na-K-Cl cotransport activity, comprising 50% of the total K influx. Activity of the cotransporter was stimulated by agents that elevate intracellular Ca and by hypertonicity and was inhibited by agents that elevate adenosine 3',5'-cyclic monophosphate, guanosine 3',5'-cyclic monophosphate, or activate protein kinase C. Exposure of the cells to primary astrocyte- or C6 glial cell-CM but not A7r5 or A10 vascular smooth muscle cell-CM also increased cotransport activity. However, this effect required > 1 h of exposure to CM, was additive with the effects of vasopressin, calcium ionophore, and hypertonicity, and was blocked by the protein synthesis inhibitor cycloheximide.(ABSTRACT TRUNCATED AT 250 WORDS)
脑微血管内皮细胞在调节血液与脑间质之间的离子和液体移动中起重要作用。已表明星形胶质细胞可诱导内皮细胞形成血脑屏障特性,包括紧密连接的形成以及酶和离子转运系统表达的增加和不对称分布。先前的研究表明,牛主动脉内皮细胞拥有一个高度活跃的钠 - 钾 - 氯共转运系统,该系统参与细胞内体积调节。本研究旨在评估脑微血管内皮细胞的钠 - 钾 - 氯共转运活性,并确定星形胶质细胞条件培养基(CM)是否影响这些细胞的钠 - 钾 - 氯共转运活性。我们发现脑微血管内皮细胞表现出强大的钠 - 钾 - 氯共转运活性,占总钾流入量的50%。共转运体的活性受到升高细胞内钙的试剂和高渗的刺激,并受到升高3',5'-环磷酸腺苷、3',5'-环磷酸鸟苷或激活蛋白激酶C的试剂的抑制。将细胞暴露于原代星形胶质细胞或C6胶质细胞的CM中,但不包括A7r5或A10血管平滑肌细胞的CM,也会增加共转运活性。然而,这种效应需要暴露于CM超过1小时,与血管加压素、钙离子载体和高渗的效应相加,并被蛋白质合成抑制剂环己酰亚胺阻断。(摘要截短于250字)