A Comparison Of Calcium-Activated Potassium Channel Currents In Cell-Attached And Excised Patches

• Type of Material: Article
• Authors: Barry S. Pallotta, University of North Carolina at Chapel Hill; John R Hepler, Emory University; Scott A. Oglesby, University of North Carolina at Chapel Hill; Kendall Harden, University of North Carolina at Chapel Hill
• Language: English
• Date: 1987-06-01
• Publisher: Rockefeller University Press
• Publication Version: Final Published Version
• Copyright Statement: © 1987, Rockefeller University Press., All rights reserved.
• Final Published Version (URL): http://dx.doi.org/10.1085/jgp.89.6.985
• Title of Journal or Parent Work: Journal of General Physiology
• ISSN: 0022-1295
• Volume: 89
• Issue: 6
• Start Page: 985
• End Page: 997
• Keywords: Life Sciences & Biomedicine; Physiology; Science & Technology

Abstract

Single channel currents from Ca-activated K channels were recorded from cell-attached patches, which were then excised from 1321N1 human astrocytoma cells. Cells were depolarized with K (110 mM) so that the membrane potential was known in both patch configurations, and the Ca ionophore A23187 or ionomycin (20-100 µM) was used to equilibrate intracellular and extracellular [Ca] (0.3 or µM). Measurements of intracellular [Ca] with the fluorescent Ca indicator quin2 verified that [Ca] equilibration apparently occurred in our experiments. Under these conditions, where both membrane potential and intracellular [Ca] were known, we found that the dependence of the channel percent open time on membrane potential and [Ca] was similar in both the cell-attached and excised patch configuration for several minutes after excision. Current-voltage relations were also similar, and autocorrelation functions constructed from the single channel currents revealed no obvious change in channel gating upon patch excision. These findings suggest that the results of studies that use excised membrane patches can be extrapolated to the K-depolarized cell-attached configuration, and that the relation between [Ca] and channel activity can be used to obtain a quantitative measure of [Ca] near the membrane intracellular surface.