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

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

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Review

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

C F Higgins. J Physiol. 1995 Jan.

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.

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References

    1. FEBS Lett. 1992 Jun 15;304(2-3):233-6 - PubMed
    1. Nature. 1992 Mar 19;356(6366):238-41 - PubMed
    1. Cell. 1992 Oct 2;71(1):23-32 - PubMed
    1. EMBO J. 1992 Dec;11(12):4291-303 - PubMed
    1. Nature. 1992 Dec 24-31;360(6406):759-62 - PubMed

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