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Local calcium transients triggered by single L-type calcium channel currents in cardiac cells.

, , , and . Science, 268 (5213): 1042--1045 (May 1995)

Abstract

Excitation-contraction coupling was studied in mammalian cardiac cells in which the opening probability of L-type calcium (Ca$^2+$) channels was reduced. Confocal microscopy during voltage-clamp depolarization revealed distinct local transients in the concentration of intracellular calcium ions (Ca$^2+$i). When voltage was varied, the latency to occurrence and the relative probability of occurrence of local Ca$^2+$i transients varied as predicted if Ca$^2+$ release from the sarcoplasmic reticulum (SR) was linked tightly to Ca$^2+$ flux through L-type Ca$^2+$ channels but not to that through the Na-Ca exchanger or to average Ca$^2+$i. Voltage had no effect on the amplitude of local Ca$^2+$i transients. Thus, the most efficacious "Ca$^2+$ signal" for activating Ca$^2+$ release from the SR may be a transient microdomain of high Ca$^2+$i beneath an individual, open L-type Ca$^2+$ channel.

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