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与多药耐药P-糖蛋白相关的容积激活氯电流

Volume-activated chloride currents associated with the multidrug resistance P-glycoprotein.

作者信息

Higgins C F

机构信息

Nuffield Department of Clinical Biochemistry, University of Oxford, John Radcliffe Hospital.

出版信息

J Physiol. 1995 Jan;482(P):31S-36S. doi: 10.1113/jphysiol.1995.sp020562.

Abstract

The ability to regulate volume is an important property of most, if not all cells. In epithelial cells, amongst others, cell volume-activated chloride channels are central to this response. The molecular identities of these channels are not yet known. Expression of the human multidrug resistance P-glycoprotein (P-gp) has been associated with cell volume-regulated chloride currents, although the nature of this association is the subject of debate. Recent data indicate that P-gp acts by regulating the activation of an endogenous channel protein. In this review, evidence associating P-gp with cell volume-activated chloride currents, and the possible mechanisms by which this might be achieved, are discussed.

摘要

调节体积的能力是大多数(即便不是全部)细胞的一项重要特性。在众多细胞类型中,上皮细胞的细胞体积激活氯通道对于这种反应至关重要。这些通道的分子身份尚不清楚。人类多药耐药P-糖蛋白(P-gp)的表达与细胞体积调节氯电流有关,尽管这种关联的本质仍存在争议。最近的数据表明,P-gp通过调节内源性通道蛋白的激活来发挥作用。在这篇综述中,我们讨论了将P-gp与细胞体积激活氯电流相关联的证据,以及实现这种关联的可能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12c1/1334234/23d02a2c56f5/jphysiol00332-0085-a.jpg

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