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PMID: 7905783 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

P-glycoprotein-associated Cl- currents are activated by cell swelling but do not contribute to cell volume regulation.

Cancer research ·Vol. 54 ·No. 3 ·1994-02-01 ·Pages 618-22

Altenberg GA, Deitmer JW, Glass DC, Reuss L

Abstract

P-glycoprotein-associated Cl- conductance is activated by cell swelling; the ensuing Cl- efflux is thought to contribute to cell volume regulation. We tested this hypothesis in human breast cancer cells transfected with human mdr1 complementary DNA, which display P-glycoprotein-associated, swelling-activated Cl- currents. The Cl- electrochemical driving force favors Cl- efflux, but there was no appreciable Cl- loss or regulatory volume decrease (both assessed with fluorescent dyes) during the exposure to hyposmotic solution. Calculations indicate that the swelling-activated Cl- current is insufficient to cause a significant Cl- efflux. Hence, regulatory volume decrease is not a function of P-glycoprotein.

Related Genes
MeSH Terms
ATP Binding Cassette Transporter, Subfamily B, Member 1 Breast Neoplasms/metabolism,pathology,physiopathology Carrier Proteins/physiology Cell Membrane Permeability Cell Size/physiology Chloride Channels/physiology Chlorides/metabolism,pharmacokinetics Drug Resistance Electrochemistry Female Humans Hypotonic Solutions Intracellular Fluid/metabolism Kinetics Membrane Glycoproteins/physiology Membrane Potentials/physiology Potassium/metabolism Transfection Tumor Cells, Cultured
Chemicals
ATP Binding Cassette Transporter, Subfamily B, Member 1 Carrier Proteins Chloride Channels Chlorides Hypotonic Solutions Membrane Glycoproteins Potassium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Altenberg G A
Department of Physiology and Biophysics, University of Texas Medical Branch, Galveston 77555-0641.
Deitmer J W
Glass D C
Reuss L
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1994-02-01
Pages
618-22
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NIDDK NIH HHS · DK08865 · United States
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