Differences between femoral artery and vein smooth muscle cells in volume-regulated chloride channels

The purpose of the present study was to compare the differences between the role of volume-regulated Cl – channels (VRCCs) in veins and arteries. We used the whole cell patch clamp and fluorescence imaging techniques to evaluate swelling-induced Cl – current (I Cl,vol ) and changes in the intracellu...

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Published inCanadian journal of physiology and pharmacology Vol. 90; no. 11; pp. 1516 - 1526
Main Authors KANG, Xiao-Long, MIN ZHANG, JIE LIU, LV, Xiao-Fei, TANG, Yong-Bo, GUAN, Yong-Yuan
Format Journal Article
LanguageEnglish
Published Plattsburgh, NY NRC Research Press 01.11.2012
National Research Council of Canada
Canadian Science Publishing NRC Research Press
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Summary:The purpose of the present study was to compare the differences between the role of volume-regulated Cl – channels (VRCCs) in veins and arteries. We used the whole cell patch clamp and fluorescence imaging techniques to evaluate swelling-induced Cl – current (I Cl,vol ) and changes in the intracellular concentrations of Cl – ([Cl – ] i ) induced by hypotonic solutions in rat femoral artery cells (FASMCs) and vein smooth muscle cells (FVSMCs). I Cl,vol and [Cl – ] i decline induced by hypotonic solution were more prominent in FASMCs than in FVSMCs. I Cl,vol and the alterations in [Cl – ] i were gradually increased as the number of cell passages increased. However, the regulatory function of tyrosine protein phosphorylation in volume-regulated chloride movement is prominent in veins. The expression of ClC-3 was higher in FASMCs than in FVSMCs. VRCC activity is more pronounced in rat femoral arteries than in veins. VRCC activity and tyrosine protein phosphorylation regulative function increase gradually as vascular cells switch from contractile to proliferative phenotypes.
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ISSN:0008-4212
1205-7541
DOI:10.1139/y2012-117