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ATP 激活的氯离子通道被一种针对 P 糖蛋白的抗体所抑制。

ATP-activated chloride channel inhibited by an antibody to P glycoprotein.

作者信息

Zhang J J, Jacob T J

机构信息

Department of Physiology, University of Wales, Cardiff, United Kingdom.

出版信息

Am J Physiol. 1994 Oct;267(4 Pt 1):C1095-102. doi: 10.1152/ajpcell.1994.267.4.C1095.

Abstract

In this report, we present the characteristics of a Cl- channel found in lens fiber cells. The single channel has a conductance of 17 pS, a linear current-voltage curve, is activated by ATP or strong depolarization and is blocked by verapamil, quinidine, 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid, 5-nitro-2-(3- phenylpropylamino)benzoate, dideoxyforskolin, and tamoxifen. These properties are similar to those reported for a volume-activated Cl- channel associated with the multidrug resistance (MDR) gene product, P glycoprotein (24). Confirming this connection, we demonstrate that our lens Cl- channel is inhibited by an antibody to P glycoprotein. The data we present here may, therefore, be the first characterization of the single channel activity of the Cl- channel associated with P glycoprotein.

摘要

在本报告中,我们展示了在晶状体纤维细胞中发现的一种氯离子通道的特性。该单通道电导为17皮安,电流-电压曲线呈线性,可被ATP或强去极化激活,并被维拉帕米、奎尼丁、4,4'-二异硫氰基芪-2,2'-二磺酸、5-硝基-2-(3-苯丙基氨基)苯甲酸酯、双脱氧佛司可林和他莫昔芬阻断。这些特性与报道的与多药耐药性(MDR)基因产物P糖蛋白相关的容积激活氯离子通道的特性相似(24)。为证实这种联系,我们证明我们的晶状体氯离子通道被抗P糖蛋白抗体抑制。因此,我们在此展示的数据可能是与P糖蛋白相关的氯离子通道单通道活性的首次特征描述。

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