Praetorius Jeppe, Nielsen Søren
The Water and Salt Research Center, Institute of Anatomy, Univ. of Aarhus, Wilhelm Meyers Allé, Bldg. 234, 8000 Aarhus C, Denmark.
Am J Physiol Cell Physiol. 2006 Jul;291(1):C59-67. doi: 10.1152/ajpcell.00433.2005. Epub 2006 Feb 15.
The choroid plexus epithelium secretes electrolytes and fluid in the brain ventricular lumen at high rates. Several channels and ion carriers have been identified as likely mediators of this transport in rodent choroid plexus. This study aimed to map several of these proteins to the human choroid plexus. Immunoperoxidase-histochemistry was employed to determine the cellular and subcellular localization of the proteins. The water channel, aquaporin (AQP) 1, was predominantly situated in the apical plasma membrane domain, although distinct basolateral and endothelial immunoreactivity was also observed. The Na(+)-K(+)-ATPase alpha(1)-subunit was exclusively localized apically in the human choroid plexus epithelial cells. Immunoreactivity for the Na(+)-K(+)-2Cl(-) cotransporter, NKCC1, was likewise confined to the apical plasma membrane domain of the epithelium. The Cl(-)/HCO(3)(-) exchanger, AE2, was localized basolaterally, as was the Na(+)-dependent Cl(-)/HCO(3)(-) exchanger, NCBE, and the electroneutral Na(+)-HCO(3)(-) cotransporter, NBCn1. No immunoreactivity was found toward the Na(+)-dependent acid/base transporters NHE1 or NBCe2. Hence, the human choroid plexus epithelium displays an almost identical distribution pattern of water channels and Na(+) transporters as the rat and mouse choroid plexus. This general cross species pattern suggests central roles for these transporters in choroid plexus functions such as cerebrospinal fluid production.
脉络丛上皮细胞以高速率在脑室腔中分泌电解质和液体。在啮齿动物脉络丛中,已确定几种通道和离子载体可能是这种转运的介质。本研究旨在将其中几种蛋白质定位到人类脉络丛。采用免疫过氧化物酶组织化学法来确定这些蛋白质的细胞和亚细胞定位。水通道水通道蛋白(AQP)1主要位于顶端质膜结构域,不过也观察到了明显的基底外侧和内皮免疫反应性。Na(+)-K(+)-ATP酶α(1)亚基仅顶端定位在人类脉络丛上皮细胞中。Na(+)-K(+)-2Cl(-)协同转运蛋白NKCC1的免疫反应性同样局限于上皮细胞的顶端质膜结构域。Cl(-)/HCO(3)(-)交换体AE2定位于基底外侧,Na(+)-依赖性Cl(-)/HCO(3)(-)交换体NCBE以及电中性Na(+)-HCO(3)(-)协同转运蛋白NBCn1也是如此。未发现针对Na(+)-依赖性酸碱转运蛋白NHE1或NBCe2的免疫反应性。因此,人类脉络丛上皮细胞显示出与大鼠和小鼠脉络丛几乎相同的水通道和Na(+)转运蛋白分布模式。这种一般的跨物种模式表明这些转运蛋白在脉络丛功能如脑脊液生成中起核心作用。