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Volume-activated chloride current is not related to P-glycoprotein overexpression.

作者信息

Dong Y, Chen K G, Durán G E, Kouyama K, Chao A C, Sikic B I, Gollapudi S V, Gupta S, Gardner P

机构信息

Department of Molecular Pharmacology, Stanford University, California 94305.

出版信息

Cancer Res. 1994 Oct 1;54(19):5029-32.

PMID:7923110
Abstract

It has been suggested that P-glycoprotein (P-gp), an ATP-dependent transporter responsible for classical multidrug resistance, is also a volume-regulated chloride channel. We reexamined this hypothesis by use of whole-cell patch clamp recordings of three matched pairs of cell lines, which were either drug-sensitive or drug-resistant due to P-gp overexpression. We demonstrate here that volume-regulated chloride-selective currents can be induced in cells with or without P-gp expression. Overexpression of either P-gp or cystic fibrosis transmembrane conductance regulator, the protein product of the CF gene and another member of the ATP-dependent transporters, is associated with a hypotonicity-induced, rapid onset, transient current prior to onset of the volume-sensitive chloride-selective current, an apparent nonspecific effect related to the overexpression of an integral membrane protein. These results suggest that there is no relationship between P-gp and the chloride channel activated by cell swelling.

摘要

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