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大鼠肝胆小管质膜中隐匿性钠钾ATP酶活性:其来源于基底外侧的证据

Cryptic Na+,K(+)-ATPase activity in rat liver canalicular plasma membranes: evidence for its basolateral origin.

作者信息

Sellinger M, Barrett C, Malle P, Gordon E R, Boyer J L

机构信息

Liver Center, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

Hepatology. 1990 Feb;11(2):223-9. doi: 10.1002/hep.1840110211.

Abstract

Controversy exists concerning the localization of the enzyme Na+,K(+)-ATPase to canalicular membranes in hepatocytes. Most studies find enzyme activity only at the basolateral plasma membrane domain of the hepatocyte. However, Na+,K(+)-ATPase activity has been detected recently in a canalicular membrane fraction prepared by Mg++ precipitation, suggesting that differences in membrane domain fluidity account for these discrepancies. To reinvestigate this question, we used free-flow electrophoresis to further purify canalicular liver plasma membranes originally separated by sucrose density centrifugation. With this technique, canalicular membranes devoid of Na+,K(+)-ATPase activity by routine assay were separated into six subfractions. More than 80% of the activities of canalicular marker enzymes was recovered in two subfractions closest to the anode, which were totally devoid of Na+,K(+)-ATPase activity. However, Na+,K(+)-ATPase activity could now be detected in the four other fractions that contained only small amounts of canalicular marker enzymes. The basolateral marker enzyme, glucagon-stimulated adenyl cyclase, comigrated with this cryptic Na+,K(+)-ATPase activity. Furthermore, addition of 6 mumol/L [12-(2-methoxyethoxy)-ethyl-8-(cis-2-n-octylcyclopropyl)-octanoate ], a membrane-fluidizing agent, to the original canalicular membrane preparation and to all subfractions did not stimulate or unmask latent Na+,K(+)-ATPase activity. Finally, when canalicular membranes isolated by Mg++ precipitation were subjected to free-flow electrophoresis, they could not be separated from the more positively charged Na+,K(+)-ATPase-containing fractions, probably because of alterations in surface charge. Together these findings suggest that Na+,K(+)-ATPase is a basolateral enzyme, that represents a small contaminant when present in canalicular liver plasma membranes and that methodological differences may account for previous discrepancies.

摘要

关于Na +,K(+)-ATP酶在肝细胞胆小管膜上的定位存在争议。大多数研究仅在肝细胞的基底外侧质膜区域发现酶活性。然而,最近在通过Mg ++沉淀制备的胆小管膜组分中检测到了Na +,K(+)-ATP酶活性,这表明膜区域流动性的差异是造成这些差异的原因。为了重新研究这个问题,我们使用自由流动电泳进一步纯化最初通过蔗糖密度离心分离的胆小管肝质膜。通过这项技术,常规检测无Na +,K(+)-ATP酶活性的胆小管膜被分离成六个亚组分。超过80%的胆小管标记酶活性在最靠近阳极的两个亚组分中被回收,这两个亚组分完全没有Na +,K(+)-ATP酶活性。然而,现在在仅含有少量胆小管标记酶的其他四个组分中可以检测到Na +,K(+)-ATP酶活性。基底外侧标记酶,胰高血糖素刺激的腺苷酸环化酶,与这种隐匿的Na +,K(+)-ATP酶活性一起迁移。此外,向原始胆小管膜制剂和所有亚组分中添加6 μmol/L [12-(2-甲氧基乙氧基)-乙基-8-(顺式-2-正辛基环丙基)-辛酸酯],一种膜流化剂,不会刺激或揭示潜在的Na +,K(+)-ATP酶活性。最后,当通过Mg ++沉淀分离的胆小管膜进行自由流动电泳时,它们无法与带正电荷更多的含Na +,K(+)-ATP酶的组分分离,这可能是由于表面电荷的改变。这些发现共同表明,Na +,K(+)-ATP酶是一种基底外侧酶,当存在于胆小管肝质膜中时是一种小污染物,并且方法学差异可能是以前差异的原因。

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