Cardiac calcium channels in planar lipid bilayers. L-type channels and calcium-permeable channels open at negative membrane potentials.
Open Access
- 1 July 1988
- journal article
- research article
- Published by Rockefeller University Press in The Journal of general physiology
- Vol. 92 (1) , 27-54
- https://doi.org/10.1085/jgp.92.1.27
Abstract
Planar lipid bilayer recordings were used to study Ca channels from bovine cardiac sarcolemmal membranes. Ca channel activity was recorded in the absence of nucleotides or soluble enzymes, over a range of membrane potentials and ionic conditions that cannot be achieved in intact cells. The dihydropyridine-sensitive L-type Ca channel, studied in the presence of Bay K 8644, was identified by a detailed comparison of its properties in artificial membranes and in intact cells. L-type Ca channels in bilayers showed voltage dependence of channel activation and inactivation, open and closed times, and single-channel conductances in Ba2+ and Ca2+ very similar to those found in cell-attached patch recordings. Open channels were blocked by micromolar concentrations of external Cd2+. In this cell-free system, channel activity tended to decrease during the course of an experiment, reminiscent of Ca2+ channel "rundown" in whole-cell and excised-patch recordings. A purely voltage-dependent component of inactivation was observed in the absence of Ca2+ stores or changes in intracellular Ca2+. Millimolar internal Ca2+ reduced unitary Ba2+ influx but did not greatly increase the rate or extent of inactivation or the rate of channel rundown. In symmetrical Ba2+ solutions, unitary conductance saturated as the Ba2+ concentration was increased up to 500 mM. The bilayer recordings also revealed activity of a novel Ca2+-permeable channel, termed "B-type" because it may contribute a steady background current at negative membrane potentials, which is distinct from L-type or T-type Ca channels previously reported. Unlike L-type channels, B-type channels have a small unitary Ba2+ conductance (7 pS), but do not discriminate between Ba2+ and Ca2+, show no obvious sensitivity to Bay K 8644, and do not run down. Unlike either L- or T-type channels, B-type channels did not require a depolarization for activation and displayed mean open times of greater than 100 ms.This publication has 63 references indexed in Scilit:
- Calcium and barium permeable channels fromAplysia nervous system reconstituted in lipid bilayersThe Journal of Membrane Biology, 1987
- Mechanisms of calcium channel modulation by β-adrenergic agents and dihydropyridine calcium agonistsJournal of Molecular and Cellular Cardiology, 1986
- Insulation of the conduction pathway of muscle transverse tubule calcium channels from the surface charge of bilayer phospholipid.The Journal of general physiology, 1986
- Sarcoplasmic reticulum contains adenine nucleotide-activated calcium channelsNature, 1985
- β-Adrenergic modulation of calcium channels in frog ventricular heart cellsNature, 1984
- Novel dihydropyridines with positive inotropic action through activation of Ca2+ channelsNature, 1983
- Mechanism of calcium channel blockade by verapamil, D600, diltiazem and nitrendipine in single dialysed heart cellsNature, 1983
- A binding-site model for calcium channel inactivation that depends on calcium entryProceedings of the Royal Society of London. B. Biological Sciences, 1982
- Properties of single calcium channels in cardiac cell cultureNature, 1982
- Reconstitution in planar lipid bilayers of a Ca2+-dependent K+ channel from transverse tubule membranes isolated from rabbit skeletal muscle.Proceedings of the National Academy of Sciences, 1982