Abstract
Fast two-dimensional confocal microscopy and the Ca(2+) indicator fluo-4 were used to study excitation-contraction (E-C) coupling in cat atrial myocytes which lack transverse tubules and contain both subsarcolemmal junctional (j-SR) and central nonjunctional (nj-SR) sarcoplasmic reticulum. Action potentials elicited by field stimulation induced transient increases of intracellular Ca(2+) concentration ([Ca(2+)](i)) that were highly inhomogeneous. Increases started at distinct subsarcolemmal release sites spaced approximately 2 microm apart. The amplitude and the latency of Ca(2+) release from these sites varied from beat to beat. Subsarcolemmal release fused to build a peripheral ring of elevated [Ca(2+)](i), which actively propagated to the center of the cells via Ca(2+)-induced Ca(2+) release. Resting myocytes exhibited spontaneous Ca(2+) release events, including Ca(2+) sparks and local (microscopic) or global (macroscopic) [Ca(2+)](i) waves. The microscopic [Ca(2+)](i) waves propagated in a saltatory fashion along the sarcolemma ("coupled" Ca(2+) sparks) revealing the sequential activation of Ca(2+) release sites of the j-SR. Moreover, during global [Ca(2+)](i) waves, Ca(2+) release was evident from individual nj-SR sites. Ca(2+) release sites were arranged in a regular three-dimensional grid as deduced from the functional data and shown by immunostaining of ryanodine receptor Ca(2+) release channels. The longitudinal and transverse distances between individual Ca(2+) release sites were both approximately 2 microm. Furthermore, electron microscopy revealed a continuous sarcotubular network and one peripheral coupling of j-SR with the sarcolemma per sarcomere. The results demonstrate directly that, in cat atrial myocytes, the action potential-induced whole-cell [Ca(2+)](i) transient is the spatio-temporal summation of Ca(2+) release from subsarcolemmal and central sites. First, j-SR sites are activated in a stochastic fashion by the opening of voltage-dependent sarcolemmal Ca(2+) channels. Subsequently, nj-SR sites are activated by Ca(2+)-induced Ca(2+) release propagating from the periphery.
Full Text
The Full Text of this article is available as a PDF (3.8 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Berlin J. R. Spatiotemporal changes of Ca2+ during electrically evoked contractions in atrial and ventricular cells. Am J Physiol. 1995 Sep;269(3 Pt 2):H1165–H1170. doi: 10.1152/ajpheart.1995.269.3.H1165. [DOI] [PubMed] [Google Scholar]
- Blatter L. A., Hüser J., Ríos E. Sarcoplasmic reticulum Ca2+ release flux underlying Ca2+ sparks in cardiac muscle. Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):4176–4181. doi: 10.1073/pnas.94.8.4176. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cannell M. B., Cheng H., Lederer W. J. Spatial non-uniformities in [Ca2+]i during excitation-contraction coupling in cardiac myocytes. Biophys J. 1994 Nov;67(5):1942–1956. doi: 10.1016/S0006-3495(94)80677-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carl S. L., Felix K., Caswell A. H., Brandt N. R., Ball W. J., Jr, Vaghy P. L., Meissner G., Ferguson D. G. Immunolocalization of sarcolemmal dihydropyridine receptor and sarcoplasmic reticular triadin and ryanodine receptor in rabbit ventricle and atrium. J Cell Biol. 1995 May;129(3):673–682. doi: 10.1083/jcb.129.3.673. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cheng H., Cannell M. B., Lederer W. J. Propagation of excitation-contraction coupling into ventricular myocytes. Pflugers Arch. 1994 Oct;428(3-4):415–417. doi: 10.1007/BF00724526. [DOI] [PubMed] [Google Scholar]
- Cheng H., Lederer M. R., Xiao R. P., Gómez A. M., Zhou Y. Y., Ziman B., Spurgeon H., Lakatta E. G., Lederer W. J. Excitation-contraction coupling in heart: new insights from Ca2+ sparks. Cell Calcium. 1996 Aug;20(2):129–140. doi: 10.1016/s0143-4160(96)90102-5. [DOI] [PubMed] [Google Scholar]
- Cheng H., Lederer W. J., Cannell M. B. Calcium sparks: elementary events underlying excitation-contraction coupling in heart muscle. Science. 1993 Oct 29;262(5134):740–744. doi: 10.1126/science.8235594. [DOI] [PubMed] [Google Scholar]
- Cleemann L., Wang W., Morad M. Two-dimensional confocal images of organization, density, and gating of focal Ca2+ release sites in rat cardiac myocytes. Proc Natl Acad Sci U S A. 1998 Sep 1;95(18):10984–10989. doi: 10.1073/pnas.95.18.10984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cordeiro J. M., Spitzer K. W., Giles W. R., Ershler P. E., Cannell M. B., Bridge J. H. Location of the initiation site of calcium transients and sparks in rabbit heart Purkinje cells. J Physiol. 2001 Mar 1;531(Pt 2):301–314. doi: 10.1111/j.1469-7793.2001.0301i.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Genka C., Ishida H., Ichimori K., Hirota Y., Tanaami T., Nakazawa H. Visualization of biphasic Ca2+ diffusion from cytosol to nucleus in contracting adult rat cardiac myocytes with an ultra-fast confocal imaging system. Cell Calcium. 1999 Mar;25(3):199–208. doi: 10.1054/ceca.1999.0026. [DOI] [PubMed] [Google Scholar]
- Györke I., Györke S. Regulation of the cardiac ryanodine receptor channel by luminal Ca2+ involves luminal Ca2+ sensing sites. Biophys J. 1998 Dec;75(6):2801–2810. doi: 10.1016/S0006-3495(98)77723-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hatem S. N., Bénardeau A., Rücker-Martin C., Marty I., de Chamisso P., Villaz M., Mercadier J. J. Different compartments of sarcoplasmic reticulum participate in the excitation-contraction coupling process in human atrial myocytes. Circ Res. 1997 Mar;80(3):345–353. doi: 10.1161/01.res.80.3.345. [DOI] [PubMed] [Google Scholar]
- Hüser J., Lipsius S. L., Blatter L. A. Calcium gradients during excitation-contraction coupling in cat atrial myocytes. J Physiol. 1996 Aug 1;494(Pt 3):641–651. doi: 10.1113/jphysiol.1996.sp021521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hüser J., Wang Y. G., Sheehan K. A., Cifuentes F., Lipsius S. L., Blatter L. A. Functional coupling between glycolysis and excitation-contraction coupling underlies alternans in cat heart cells. J Physiol. 2000 May 1;524(Pt 3):795–806. doi: 10.1111/j.1469-7793.2000.00795.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lipp P., Hüser J., Pott L., Niggli E. Spatially non-uniform Ca2+ signals induced by the reduction of transverse tubules in citrate-loaded guinea-pig ventricular myocytes in culture. J Physiol. 1996 Dec 15;497(Pt 3):589–597. doi: 10.1113/jphysiol.1996.sp021792. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lipp P., Pott L., Callewaert G., Carmeliet E. Simultaneous recording of Indo-1 fluorescence and Na+/Ca2+ exchange current reveals two components of Ca2(+)-release from sarcoplasmic reticulum of cardiac atrial myocytes. FEBS Lett. 1990 Nov 26;275(1-2):181–184. doi: 10.1016/0014-5793(90)81467-3. [DOI] [PubMed] [Google Scholar]
- López-López J. R., Shacklock P. S., Balke C. W., Wier W. G. Local, stochastic release of Ca2+ in voltage-clamped rat heart cells: visualization with confocal microscopy. J Physiol. 1994 Oct 1;480(Pt 1):21–29. doi: 10.1113/jphysiol.1994.sp020337. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mackenzie L., Bootman M. D., Berridge M. J., Lipp P. Predetermined recruitment of calcium release sites underlies excitation-contraction coupling in rat atrial myocytes. J Physiol. 2001 Feb 1;530(Pt 3):417–429. doi: 10.1111/j.1469-7793.2001.0417k.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McNutt N. S., Fawcett D. W. The ultrastructure of the cat myocardium. II. Atrial muscle. J Cell Biol. 1969 Jul;42(1):46–67. doi: 10.1083/jcb.42.1.46. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Niggli E. Localized intracellular calcium signaling in muscle: calcium sparks and calcium quarks. Annu Rev Physiol. 1999;61:311–335. doi: 10.1146/annurev.physiol.61.1.311. [DOI] [PubMed] [Google Scholar]
- Pott L., Lipp P., Callewaert G., Carmeliet E. Spatial properties of Ca2+ transients in cardiac myocytes studied by simultaneous measurement of Na(+)-Ca2+ exchange current and indo-1 fluorescence. Ann N Y Acad Sci. 1991;639:354–365. doi: 10.1111/j.1749-6632.1991.tb17324.x. [DOI] [PubMed] [Google Scholar]
- REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Santana L. F., Cheng H., Gómez A. M., Cannell M. B., Lederer W. J. Relation between the sarcolemmal Ca2+ current and Ca2+ sparks and local control theories for cardiac excitation-contraction coupling. Circ Res. 1996 Jan;78(1):166–171. doi: 10.1161/01.res.78.1.166. [DOI] [PubMed] [Google Scholar]
- Scriven D. R., Dan P., Moore E. D. Distribution of proteins implicated in excitation-contraction coupling in rat ventricular myocytes. Biophys J. 2000 Nov;79(5):2682–2691. doi: 10.1016/S0006-3495(00)76506-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shacklock P. S., Wier W. G., Balke C. W. Local Ca2+ transients (Ca2+ sparks) originate at transverse tubules in rat heart cells. J Physiol. 1995 Sep 15;487(Pt 3):601–608. doi: 10.1113/jphysiol.1995.sp020903. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sipido K. R., Wier W. G. Flux of Ca2+ across the sarcoplasmic reticulum of guinea-pig cardiac cells during excitation-contraction coupling. J Physiol. 1991 Apr;435:605–630. doi: 10.1113/jphysiol.1991.sp018528. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Soeller C., Cannell M. B. Examination of the transverse tubular system in living cardiac rat myocytes by 2-photon microscopy and digital image-processing techniques. Circ Res. 1999 Feb 19;84(3):266–275. doi: 10.1161/01.res.84.3.266. [DOI] [PubMed] [Google Scholar]
- Song L. S., Sham J. S., Stern M. D., Lakatta E. G., Cheng H. Direct measurement of SR release flux by tracking 'Ca2+ spikes' in rat cardiac myocytes. J Physiol. 1998 Nov 1;512(Pt 3):677–691. doi: 10.1111/j.1469-7793.1998.677bd.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tanaka H., Sekine T., Kawanishi T., Nakamura R., Shigenobu K. Intrasarcomere [Ca2+] gradients and their spatio-temporal relation to Ca2+ sparks in rat cardiomyocytes. J Physiol. 1998 Apr 1;508(Pt 1):145–152. doi: 10.1111/j.1469-7793.1998.145br.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wier W. G., Balke C. W. Ca(2+) release mechanisms, Ca(2+) sparks, and local control of excitation-contraction coupling in normal heart muscle. Circ Res. 1999 Oct 29;85(9):770–776. doi: 10.1161/01.res.85.9.770. [DOI] [PubMed] [Google Scholar]
- Wu J. Y., Vereecke J., Carmeliet E., Lipsius S. L. Ionic currents activated during hyperpolarization of single right atrial myocytes from cat heart. Circ Res. 1991 Apr;68(4):1059–1069. doi: 10.1161/01.res.68.4.1059. [DOI] [PubMed] [Google Scholar]