Regulation of calcium release is gated by calcium current, not gating charge, in cardiac myocytes
- PMID: 2543067
- DOI: 10.1126/science.2543067
Regulation of calcium release is gated by calcium current, not gating charge, in cardiac myocytes
Abstract
In skeletal muscle, intramembrane charge movement initiates the processes that lead to the release of calcium from the sarcoplasmic reticulum. In cardiac muscle, in contrast, the similarity of the voltage dependence of developed tension and intracellular calcium transients to that of calcium current suggests that the calcium current may gate the release of calcium. Nevertheless, a mechanism similar to that of skeletal muscle continues to be postulated for cardiac muscle. By using rapid exchange (20 to 50 milliseconds) of the extracellular solutions in rat ventricular myocytes in which the intracellular calcium transients or cell shortening were measured, it has now been shown that the influx of calcium through the calcium channel is a mandatory link in the processes that couple membrane depolarization to the release of calcium. Thus, intramembrane charge movement does not contribute to the release of calcium in heart muscle.
Comment in
-
Does voltage affect excitation-contraction coupling in the heart?Science. 1989 Dec 22;246(4937):1640. doi: 10.1126/science.2627235. Science. 1989. PMID: 2627235 No abstract available.
Similar articles
-
Cross-signaling between L-type Ca2+ channels and ryanodine receptors in rat ventricular myocytes.J Gen Physiol. 1996 Nov;108(5):435-54. doi: 10.1085/jgp.108.5.435. J Gen Physiol. 1996. PMID: 8923268 Free PMC article.
-
Role of Ca2+ channel in cardiac excitation-contraction coupling in the rat: evidence from Ca2+ transients and contraction.J Physiol. 1991 Jan;432:283-312. doi: 10.1113/jphysiol.1991.sp018385. J Physiol. 1991. PMID: 1653321 Free PMC article.
-
Functional coupling of Ca2+ channels and ryanodine receptors in cardiac myocytes.Proc Natl Acad Sci U S A. 1995 Jan 3;92(1):121-5. doi: 10.1073/pnas.92.1.121. Proc Natl Acad Sci U S A. 1995. PMID: 7816800 Free PMC article.
-
Action potential duration modulates calcium influx, Na(+)-Ca2+ exchange, and intracellular calcium release in rat ventricular myocytes.Ann N Y Acad Sci. 1996 Apr 15;779:417-29. doi: 10.1111/j.1749-6632.1996.tb44817.x. Ann N Y Acad Sci. 1996. PMID: 8659858 Review.
-
Ca regulation in cardiac muscle.Med Sci Sports Exerc. 1991 Oct;23(10):1157-62. Med Sci Sports Exerc. 1991. PMID: 1661831 Review.
Cited by
-
Ca2+ current-gated focal and local Ca2+ release in rat atrial myocytes: evidence from rapid 2-D confocal imaging.J Physiol. 2002 Sep 1;543(Pt 2):439-53. doi: 10.1113/jphysiol.2002.024190. J Physiol. 2002. PMID: 12205180 Free PMC article.
-
Increased PKA activity and its influence on isoprenaline-stimulated L-type Ca2+ channels in the heart from ovariectomized rats.Br J Pharmacol. 2005 Apr;144(7):972-81. doi: 10.1038/sj.bjp.0706123. Br J Pharmacol. 2005. PMID: 15685204 Free PMC article.
-
CRISPR/Cas9 Gene editing of RyR2 in human stem cell-derived cardiomyocytes provides a novel approach in investigating dysfunctional Ca2+ signaling.Cell Calcium. 2018 Jul;73:104-111. doi: 10.1016/j.ceca.2018.04.009. Epub 2018 Apr 27. Cell Calcium. 2018. PMID: 29730419 Free PMC article.
-
Sodium current-induced calcium signals in isolated guinea-pig ventricular myocytes.J Physiol. 1994 Feb 1;474(3):439-46. doi: 10.1113/jphysiol.1994.sp020035. J Physiol. 1994. PMID: 8014905 Free PMC article.
-
Calcium signaling consequences of RyR2 mutations associated with CPVT1 introduced via CRISPR/Cas9 gene editing in human-induced pluripotent stem cell-derived cardiomyocytes: Comparison of RyR2-R420Q, F2483I, and Q4201R.Heart Rhythm. 2021 Feb;18(2):250-260. doi: 10.1016/j.hrthm.2020.09.007. Epub 2020 Sep 12. Heart Rhythm. 2021. PMID: 32931925 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources