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Am J Physiol Cell Physiol 267: C1080-C1086, 1994;
0363-6143/94 $5.00
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AJP - Cell Physiology, Vol 267, Issue 4 C1080-C1086, Copyright © 1994 by American Physiological Society


ARTICLES

Large Ca(2+)-activated K+ channels responsive to angiotensin II in cultured human mesangial cells

J. D. Stockand and S. C. Sansom
Department of Medicine, University of Texas Health Science Center at Houston 77225.

The patch-clamp method was used to determine the properties and response to angiotensin II (ANG II) of K+ channels in subpassages of human mesangial cell cultures. In cell-attached patches, with 140 mM KCl in the bath and cell potential equal to 40 mV, the open probability (Po) of large K+ channels (MKCa) was 0.8 with 0.5 mM Ca2+ in the bath and < 0.05 if the bath Ca2+ concentration was reduced to 1.0 microM. Open and closed dwell-time histograms of MKCa displayed both fast and slow time constants. Addition of ANG II (100 nM) to the bath solution (Ca2+ = 1.0 microM) increased the Po of MKCa in cyclic bursts by decreasing the time constant of the slow closed state. In excised inside-out patches, the mean single-channel conductance of MKCa was 206 pS in symmetrical 140 mM KCl. The selectivity sequence, established in asymmetrical cationic solutions, was K+ (1.0) > Rb+ (0.54) > NH+4 (0.11) > > Cs+ = Na+ (< 0.05). The Po of MKCa was increased by depolarizing potentials and high bath Ca2+. The Boltzmann distribution was consistent with an effective valence of 1.0, and the Hill coefficient for Ca2+ activation was 0.52. We conclude that MKCa has properties similar to large Ca(2+)-activated K+ channels and may act to repolarize the membrane of mesangial cells in response to an agonist-induced mobilization of intracellular Ca2+.


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