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Received August 21, 2001
Accepted after revision November 15, 2001
1 Department of Physiology and Cell Biology and COBRE Program, University of Nevada School of Medicine, Reno, Nevada 89557-0046, USA
* To whom correspondence should be addressed. E-mail: burt{at}physio.unr.edu.
Calcium-activated chloride currents (ICl(Ca)) have been recorded in various smooth muscle cells but, to date, there has been no information as to the molecular nature of the channel underlying this conductance. We have characterised native ICl(Ca) in freshly dispersed smooth muscle cells isolated from murine portal vein using whole-cell voltage-clamp. ICl(Ca) exhibited time-dependent activation at depolarised potentials and rapid deactivation upon repolarisation. The reversal potential of ICl(Ca) was close to the theoretical equilibrium potential (ECl) and was shifted by replacement of external Cl- by SCN- or isethionate. Dithiothreitol (DTT, 1 mm), a blocker of CLCA1, had no effect on the ICl(Ca) current in myocytes. RT-PCR demonstrated the expression of mCLCA1 transcripts, but not mCLCA3 transcripts, in various murine smooth muscle cells including portal vein, as well as cardiomyocytes, and the levels of mCLCA1 transcriptional expression were quantified by real time quantitative RT-PCR. Stable transfection of HEK293 cells with the cDNA encoding mCLCA1 cloned from murine portal vein smooth muscle yielded a current with notable differences in Ca2+-sensitivity, channel kinetics and modulation by DTT from the native ICl(Ca). However, there was some similarity in the pore properties and these data suggest that mCLCA1 alone does not comprise the Cl- channel in portal vein smooth muscle cells.
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