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. 1997 Jul;73(1):141–156. doi: 10.1016/S0006-3495(97)78055-X

Heterogeneity of Ca2+ gating of skeletal muscle and cardiac ryanodine receptors.

J A Copello 1, S Barg 1, H Onoue 1, S Fleischer 1
PMCID: PMC1180916  PMID: 9199779

Abstract

The single-channel activity of rabbit skeletal muscle ryanodine receptor (skeletal RyR) and dog cardiac RyR was studied as a function of cytosolic [Ca2+]. The studies reveal that for both skeletal and cardiac RyRs, heterogeneous populations of channels exist, rather than a uniform behavior. Skeletal muscle RyRs displayed two extremes of behavior: 1) low-activity RyRs (LA skeletal RyRs, approximately 35% of the channels) had very low open probability (Po < 0.1) at all [Ca2+] and remained closed in the presence of Mg2+ (2 mM) and ATP (1 mM); 2) high-activity RyRs (HA skeletal RyRs) had much higher activity and displayed further heterogeneity in their Po values at low [Ca2+] (< 50 nM), and in their patterns of activation by [Ca2+]. Hill coefficients for activation (nHa) varied from 0.8 to 5.2. Cardiac RyRs, in comparison, behaved more homogeneously. Most cardiac RyRs were closed at 100 nM [Ca2+] and activated in a cooperative manner (nHa ranged from 1.6 to 5.0), reaching a high Po (> 0.6) in the presence and absence of Mg2+ and ATP. Heart RyRs were much less sensitive (10x) to inhibition by [Ca2+] than skeletal RyRs. The differential heterogeneity of heart versus skeletal muscle RyRs may reflect the modulation required for calcium-induced calcium release versus depolarization-induced Ca2+ release.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Armisén R., Sierralta J., Vélez P., Naranjo D., Suárez-Isla B. A. Modal gating in neuronal and skeletal muscle ryanodine-sensitive Ca2+ release channels. Am J Physiol. 1996 Jul;271(1 Pt 1):C144–C153. doi: 10.1152/ajpcell.1996.271.1.C144. [DOI] [PubMed] [Google Scholar]
  2. Ashley R. H., Williams A. J. Divalent cation activation and inhibition of single calcium release channels from sheep cardiac sarcoplasmic reticulum. J Gen Physiol. 1990 May;95(5):981–1005. doi: 10.1085/jgp.95.5.981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Barg S., Copello J. A., Fleischer S. Different interactions of cardiac and skeletal muscle ryanodine receptors with FK-506 binding protein isoforms. Am J Physiol. 1997 May;272(5 Pt 1):C1726–C1733. doi: 10.1152/ajpcell.1997.272.5.C1726. [DOI] [PubMed] [Google Scholar]
  4. Bezprozvanny I., Watras J., Ehrlich B. E. Bell-shaped calcium-response curves of Ins(1,4,5)P3- and calcium-gated channels from endoplasmic reticulum of cerebellum. Nature. 1991 Jun 27;351(6329):751–754. doi: 10.1038/351751a0. [DOI] [PubMed] [Google Scholar]
  5. Bull R., Marengo J. J. Sarcoplasmic reticulum release channels from frog skeletal muscle display two types of calcium dependence. FEBS Lett. 1993 Oct 4;331(3):223–227. doi: 10.1016/0014-5793(93)80341-q. [DOI] [PubMed] [Google Scholar]
  6. Chamberlain B. K., Levitsky D. O., Fleischer S. Isolation and characterization of canine cardiac sarcoplasmic reticulum with improved Ca2+ transport properties. J Biol Chem. 1983 May 25;258(10):6602–6609. [PubMed] [Google Scholar]
  7. Chamberlain B. K., Volpe P., Fleischer S. Calcium-induced calcium release from purified cardiac sarcoplasmic reticulum vesicles. General characteristics. J Biol Chem. 1984 Jun 25;259(12):7540–7546. [PubMed] [Google Scholar]
  8. Chu A., Fill M., Stefani E., Entman M. L. Cytoplasmic Ca2+ does not inhibit the cardiac muscle sarcoplasmic reticulum ryanodine receptor Ca2+ channel, although Ca(2+)-induced Ca2+ inactivation of Ca2+ release is observed in native vesicles. J Membr Biol. 1993 Jul;135(1):49–59. doi: 10.1007/BF00234651. [DOI] [PubMed] [Google Scholar]
  9. Coronado R., Morrissette J., Sukhareva M., Vaughan D. M. Structure and function of ryanodine receptors. Am J Physiol. 1994 Jun;266(6 Pt 1):C1485–C1504. doi: 10.1152/ajpcell.1994.266.6.C1485. [DOI] [PubMed] [Google Scholar]
  10. Dulhunty A. F., Junankar P. R., Eager K. R., Ahern G. P., Laver D. R. Ion channels in the sarcoplasmic reticulum of striated muscle. Acta Physiol Scand. 1996 Mar;156(3):375–385. doi: 10.1046/j.1365-201X.1996.193000.x. [DOI] [PubMed] [Google Scholar]
  11. Fabiato A. Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum. Am J Physiol. 1983 Jul;245(1):C1–14. doi: 10.1152/ajpcell.1983.245.1.C1. [DOI] [PubMed] [Google Scholar]
  12. Fabiato A. Computer programs for calculating total from specified free or free from specified total ionic concentrations in aqueous solutions containing multiple metals and ligands. Methods Enzymol. 1988;157:378–417. doi: 10.1016/0076-6879(88)57093-3. [DOI] [PubMed] [Google Scholar]
  13. Fleischer S., Inui M. Biochemistry and biophysics of excitation-contraction coupling. Annu Rev Biophys Biophys Chem. 1989;18:333–364. doi: 10.1146/annurev.bb.18.060189.002001. [DOI] [PubMed] [Google Scholar]
  14. Hain J., Nath S., Mayrleitner M., Fleischer S., Schindler H. Phosphorylation modulates the function of the calcium release channel of sarcoplasmic reticulum from skeletal muscle. Biophys J. 1994 Nov;67(5):1823–1833. doi: 10.1016/S0006-3495(94)80664-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Hain J., Onoue H., Mayrleitner M., Fleischer S., Schindler H. Phosphorylation modulates the function of the calcium release channel of sarcoplasmic reticulum from cardiac muscle. J Biol Chem. 1995 Feb 3;270(5):2074–2081. doi: 10.1074/jbc.270.5.2074. [DOI] [PubMed] [Google Scholar]
  16. Harrison S. M., Bers D. M. The effect of temperature and ionic strength on the apparent Ca-affinity of EGTA and the analogous Ca-chelators BAPTA and dibromo-BAPTA. Biochim Biophys Acta. 1987 Aug 13;925(2):133–143. doi: 10.1016/0304-4165(87)90102-4. [DOI] [PubMed] [Google Scholar]
  17. Landaw E. M., DiStefano J. J., 3rd Multiexponential, multicompartmental, and noncompartmental modeling. II. Data analysis and statistical considerations. Am J Physiol. 1984 May;246(5 Pt 2):R665–R677. doi: 10.1152/ajpregu.1984.246.5.R665. [DOI] [PubMed] [Google Scholar]
  18. Laver D. R., Roden L. D., Ahern G. P., Eager K. R., Junankar P. R., Dulhunty A. F. Cytoplasmic Ca2+ inhibits the ryanodine receptor from cardiac muscle. J Membr Biol. 1995 Sep;147(1):7–22. doi: 10.1007/BF00235394. [DOI] [PubMed] [Google Scholar]
  19. Lee Y. S., Ondrias K., Duhl A. J., Ehrlich B. E., Kim D. H. Comparison of calcium release from sarcoplasmic reticulum of slow and fast twitch muscles. J Membr Biol. 1991 Jun;122(2):155–163. doi: 10.1007/BF01872638. [DOI] [PubMed] [Google Scholar]
  20. Ma J. Desensitization of the skeletal muscle ryanodine receptor: evidence for heterogeneity of calcium release channels. Biophys J. 1995 Mar;68(3):893–899. doi: 10.1016/S0006-3495(95)80265-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Marengo J. J., Bull R., Hidalgo C. Calcium dependence of ryanodine-sensitive calcium channels from brain cortex endoplasmic reticulum. FEBS Lett. 1996 Mar 25;383(1-2):59–62. doi: 10.1016/0014-5793(96)00222-0. [DOI] [PubMed] [Google Scholar]
  22. Mayrleitner M., Timerman A. P., Wiederrecht G., Fleischer S. The calcium release channel of sarcoplasmic reticulum is modulated by FK-506 binding protein: effect of FKBP-12 on single channel activity of the skeletal muscle ryanodine receptor. Cell Calcium. 1994 Feb;15(2):99–108. doi: 10.1016/0143-4160(94)90048-5. [DOI] [PubMed] [Google Scholar]
  23. Meissner G. Adenine nucleotide stimulation of Ca2+-induced Ca2+ release in sarcoplasmic reticulum. J Biol Chem. 1984 Feb 25;259(4):2365–2374. [PubMed] [Google Scholar]
  24. Meissner G. Ryanodine receptor/Ca2+ release channels and their regulation by endogenous effectors. Annu Rev Physiol. 1994;56:485–508. doi: 10.1146/annurev.ph.56.030194.002413. [DOI] [PubMed] [Google Scholar]
  25. Nagasaki K., Kasai M. Fast release of calcium from sarcoplasmic reticulum vesicles monitored by chlortetracycline fluorescence. J Biochem. 1983 Oct;94(4):1101–1109. doi: 10.1093/oxfordjournals.jbchem.a134453. [DOI] [PubMed] [Google Scholar]
  26. O'Brien J., Valdivia H. H., Block B. A. Physiological differences between the alpha and beta ryanodine receptors of fish skeletal muscle. Biophys J. 1995 Feb;68(2):471–482. doi: 10.1016/S0006-3495(95)80208-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Ogawa Y. Role of ryanodine receptors. Crit Rev Biochem Mol Biol. 1994;29(4):229–274. doi: 10.3109/10409239409083482. [DOI] [PubMed] [Google Scholar]
  28. Percival A. L., Williams A. J., Kenyon J. L., Grinsell M. M., Airey J. A., Sutko J. L. Chicken skeletal muscle ryanodine receptor isoforms: ion channel properties. Biophys J. 1994 Nov;67(5):1834–1850. doi: 10.1016/S0006-3495(94)80665-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Pessah I. N., Waterhouse A. L., Casida J. E. The calcium-ryanodine receptor complex of skeletal and cardiac muscle. Biochem Biophys Res Commun. 1985 Apr 16;128(1):449–456. doi: 10.1016/0006-291x(85)91699-7. [DOI] [PubMed] [Google Scholar]
  30. Rousseau E., Meissner G. Single cardiac sarcoplasmic reticulum Ca2+-release channel: activation by caffeine. Am J Physiol. 1989 Feb;256(2 Pt 2):H328–H333. doi: 10.1152/ajpheart.1989.256.2.H328. [DOI] [PubMed] [Google Scholar]
  31. Rousseau E., Pinkos J., Savaria D. Functional sensitivity of the native skeletal Ca(2+)-release channel to divalent cations and the Mg-ATP complex. Can J Physiol Pharmacol. 1992 Mar;70(3):394–402. doi: 10.1139/y92-049. [DOI] [PubMed] [Google Scholar]
  32. Saito A., Seiler S., Chu A., Fleischer S. Preparation and morphology of sarcoplasmic reticulum terminal cisternae from rabbit skeletal muscle. J Cell Biol. 1984 Sep;99(3):875–885. doi: 10.1083/jcb.99.3.875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Schindler H. Planar lipid-protein membranes: strategies of formation and of detecting dependencies of ion transport functions on membrane conditions. Methods Enzymol. 1989;171:225–253. doi: 10.1016/s0076-6879(89)71014-4. [DOI] [PubMed] [Google Scholar]
  34. Sitsapesan R., Williams A. J. Gating of the native and purified cardiac SR Ca(2+)-release channel with monovalent cations as permeant species. Biophys J. 1994 Oct;67(4):1484–1494. doi: 10.1016/S0006-3495(94)80622-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Smith J. S., Coronado R., Meissner G. Single channel measurements of the calcium release channel from skeletal muscle sarcoplasmic reticulum. Activation by Ca2+ and ATP and modulation by Mg2+. J Gen Physiol. 1986 Nov;88(5):573–588. doi: 10.1085/jgp.88.5.573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Sorrentino V., Volpe P. Ryanodine receptors: how many, where and why? Trends Pharmacol Sci. 1993 Mar;14(3):98–103. doi: 10.1016/0165-6147(93)90072-r. [DOI] [PubMed] [Google Scholar]
  37. Timerman A. P., Jayaraman T., Wiederrecht G., Onoue H., Marks A. R., Fleischer S. The ryanodine receptor from canine heart sarcoplasmic reticulum is associated with a novel FK-506 binding protein. Biochem Biophys Res Commun. 1994 Jan 28;198(2):701–706. doi: 10.1006/bbrc.1994.1101. [DOI] [PubMed] [Google Scholar]
  38. Timerman A. P., Ogunbumni E., Freund E., Wiederrecht G., Marks A. R., Fleischer S. The calcium release channel of sarcoplasmic reticulum is modulated by FK-506-binding protein. Dissociation and reconstitution of FKBP-12 to the calcium release channel of skeletal muscle sarcoplasmic reticulum. J Biol Chem. 1993 Nov 5;268(31):22992–22999. [PubMed] [Google Scholar]
  39. Timerman A. P., Onoue H., Xin H. B., Barg S., Copello J., Wiederrecht G., Fleischer S. Selective binding of FKBP12.6 by the cardiac ryanodine receptor. J Biol Chem. 1996 Aug 23;271(34):20385–20391. doi: 10.1074/jbc.271.34.20385. [DOI] [PubMed] [Google Scholar]
  40. Timerman A. P., Wiederrecht G., Marcy A., Fleischer S. Characterization of an exchange reaction between soluble FKBP-12 and the FKBP.ryanodine receptor complex. Modulation by FKBP mutants deficient in peptidyl-prolyl isomerase activity. J Biol Chem. 1995 Feb 10;270(6):2451–2459. doi: 10.1074/jbc.270.6.2451. [DOI] [PubMed] [Google Scholar]
  41. Tripathy A., Xu L., Mann G., Meissner G. Calmodulin activation and inhibition of skeletal muscle Ca2+ release channel (ryanodine receptor). Biophys J. 1995 Jul;69(1):106–119. doi: 10.1016/S0006-3495(95)79880-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Tsien R. Y. New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures. Biochemistry. 1980 May 27;19(11):2396–2404. doi: 10.1021/bi00552a018. [DOI] [PubMed] [Google Scholar]
  43. Witcher D. R., Kovacs R. J., Schulman H., Cefali D. C., Jones L. R. Unique phosphorylation site on the cardiac ryanodine receptor regulates calcium channel activity. J Biol Chem. 1991 Jun 15;266(17):11144–11152. [PubMed] [Google Scholar]
  44. Zahradníková A., Bak J., Mészáros L. G. Heterogeneity of the cardiac calcium release channel as assessed by its response to ADP-ribose. Biochem Biophys Res Commun. 1995 May 16;210(2):457–463. doi: 10.1006/bbrc.1995.1682. [DOI] [PubMed] [Google Scholar]
  45. Zahradníková A., Zahradník I. Description of modal gating of the cardiac calcium release channel in planar lipid membranes. Biophys J. 1995 Nov;69(5):1780–1788. doi: 10.1016/S0006-3495(95)80048-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Zorzato F., Sacchetto R., Margreth A. Identification of two ryanodine receptor transcripts in neonatal, slow-, and fast-twitch rabbit skeletal muscles. Biochem Biophys Res Commun. 1994 Sep 30;203(3):1725–1730. doi: 10.1006/bbrc.1994.2385. [DOI] [PubMed] [Google Scholar]

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