References
Allbritton, N.L., Meyer, T. 1993. Localized calcium spikes and propagating calcium waves. Cell Calcium 14:691–697
Anholt, R.R.H. 1994. Signal integration in the nervous system: adenylate cyclases as molecular coincidence detectors. Trends Neurosci. 17:37–41
Atri, A., Amundsen, J., Clapham, D., Sneyd, J. 1993. A singlepool model for intracellular calcium oscillations and waves in the Xenopus laevis oocyte. Biophys. J. 65:1727–1739
Berridge, M.J. 1993. Inositol trisphosphate and calcium signalling. Nature 361:315–325
Berridge, M.J. 1993. A tale of two messengers. Nature 365:388–389
Berridge, M.J., Dupont, G. 1994. Spatial and temporal signalling by calcium. Curr. Op. Cell Biol. 6:267–274
Berridge, M.J., Irvine, R.F. 1984. Inositol trisphosphate, a novel second messenger in cellular signal transduction. Nature 312:315–321
Bezprozvanny, I., Ehrlich, B.E. 1993. Divalent cation conduction of the inositol 1,4,5-trisphosphate gated calcium channels of canine cerebellum. Biophys. J. 64:A328
Bezprozvanny, I., Watras, J., Ehrlich, B.E. 1991. Bell-shaped calcium-response curves for Ins(1,4,5)0115–01 and calcium-gated channels from endoplasmic reticulum of cerebellum. Nature 351:751–754
Blondel, O., Takeda, J., Janssen, H., Seino, S., Bell, G.I. 1993. Sequence and functional characterization of a third inositol trisphosphate receptor subtype, IP3R-3, expressed in pancreatic islets, kidney, gastrointestinal tract, and other tissues. J. Biol. Chem. 268:11356–11363
Brillantes, A-M.B., Ondrias, K., Jayaraman, T., Scott, A., Kobrinsky, S.E., Ehrlich, B.E., Marks, A.R. 1994. FKBP12 optimises function of the cloned expressed calcium release channel (ryanodine receptor). Biophys. J. 66:A19
Burgess, G.M., Irvine, R.F., Berridge, M.J., McKinney, J.S., Putney, J.W., Jr. 1984. Actions of inositol phosphates on calcium pools in guinea pig hepatocytes. Biochem. J. 224:741–746
Champeil, P., Combettes, L., Berthon, B., Doucet, E., Orlowski, S., Claret, M. 1989. Fast kinetics of calcium release induced by myo-inositol trisphosphate in permeabilized rat hepatocytes. J. Biol. Chem. 264:17665–17673
Chen S.R.W., Vaughan, D.M., Airey, J.A., Coronado, R., MacLennan, D.H. 1993. Functional expression of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit skeletal muscle sarcoplasmic reticulum in COS-1 cells. Biochemistry 32:3743–3753
Chen, S.R.W., Zhang, L., MacLennan, D.H. 1993. Antibodies as probes for Ca2+ activation sites on the Ca2+ release channel (ryanodine receptor) of rabbit skeletal muscle sarcoplasmic reticulum. J. Biol. Chem. 268:13414–13421
Combettes, L., Claret, M., Champeil, P. 1992. Do submaximal InsP3 concentrations only induce partial release discharge of permeabilized hepatocyte calcium pools because of the concomitant reduction of intraluminal Ca2+ concentration? FEBS Lett. 301:287–290
Danoff, S.K., Ferris, C.D., Donath, C., Fischer, G.A., Munemitsu, S., Ullrich, A., Snyder, S.H., Ross, C.A. 1991. Inositol 1,4,5-trisphosphate receptors: distinct neuronal and nonneuronal forms derived by alternative splicing differ in phosphorylation. Proc. Natl. Acad. Sci. USA 88:2951–2955
Danoff, S.K., Supattapone, S., Snyder, S.H. 1988. Characterization of a membrane protein from brain mediating the inhibition of inositol 1,4,5-trisphosphate receptor binding by calcium. Biochem. J. 254:701–705
DiPolo, I.L., Marty, A. 1994. Calcium-induced calcium release in cerebellar Purkinje cells. Neuron 12:663–673
Fabiato, A., Fabiato, F. 1979. Use of chlorotetracycline fluorescence to demonstrate Ca2+-induced release of Ca2+ from sarcoplasmic reticulum of skinned cardiac cells. Nature 281:146–148
Ferris, C.D., Cameron, A.M., Huganir, R.L., Snyder, S.H. 1992. Quantal calcium release by purified reconstituted inositol 1,4,5-trisphosphate receptors. Nature 356:350–352
Ferris, C.D., Huganir, R.L., Bredt, D.S., Cameron, A.M., Snyder, S.H. 1991. Inositol trisphosphate receptor: phosphorylation by protein kinase C and calcium calmodulin-dependent protein kinases in reconstituted lipid vesicles. Proc. Natl. Acad. Sci. USA 88:2232–2235
Ferris, C.D., Huganir, R.L., Supattapone, S., Snyder, S.H. 1989. Purified inositol 1,4,5-trisphosphate receptor mediates calcium flux in reconstituted lipid vesicles. Nature 342:87–89
Ferris, C.D., Snyder, S.H. 1992. Inositol 1,4,5-trisphosphateactivated calcium channels. Ann. Rev. Physiol. 54:469–488
Finch, E.A., Turner, T.J., Goldin, S.M. 1991. Calcium as a coagonist of inositol 1,4,5-trisphosphate-induced calcium release. Science 252:443–446
Friel, D.D., Tsien, R.W. 1992. A caffeine- and ryanodinesensitive Ca2+ store in bullfrog sympathetic neurones modulates effects of Ca2+ entry on [Ca2+]i. J. Physiol. 450:217–246
Furuichi, T., Shiota, C., Mikoshiba, K. 1990. Distribution of inositol 1,4,5-trisphosphate receptor mRNA in mouse tissues. FEBS Lett. 267:85–88
Furuichi, T., Yoshikawa, S., Miyawaki, A., Wada, K., Maeda, M., Mikoshiba, K. 1989. Primary structure and functional expression of the inositol 1,4,5-trisphosphate-binding protein P400. Nature 342:32–38
Galione, A. 1993. Cyclic ADP-ribose: a new way to control calcium. Science 259:325–326
Galione, A., McDougall, A., Busa, W.B., Willmott, N., Gillot, I., Whitaker, M. 1993. Redundant mechanisms of calcium-induced calcium release underlying calcium waves during fertilization of sea urchin eggs. Science 261:348–352
Györke, S., Palade, P. 1994. Ca2+-dependent negative control mechanism for Ca2+-induced Ca2+ release in crayfish muscle. J. Physiol. 476:315–322
Hill, T.D., Campos-Gonzalez, R., Kindman, H., Boynton, A.L. 1988. Inhibition of inositol trisphosphate-stimulated calcium mobilization by calmodulin antagonists in rat liver epithelial cells. J. Biol. Chem. 263:16479–16484
Iino, M. 1990. Biphasic Ca2+ dependence of inositol 1,4,5-trisphosphate-induced Ca release in smooth muscle cells of the guinea pig taenia caeci. J. Gen. Physiol. 95:1103–1122
Iino, M., Endo, M. 1992. Calcium-dependent immediate feedback control of inositol 1,4,5-trisphosphate-induced Ca2+ release. Nature 360:76–78
Iino, M., Yamazawa, T., Miyashita, Y., Endo, M., Kasai, H. 1993. Critical intracellular Ca2+ concentration for all-or-none Ca2+ spiking in single smooth muscle cells. EMBO J. 12:5287–5291
Ikemoto, N., Antoniu, B., Kang, J-J., Mészáros, L.G., Ronjat, M. 1991. Intravesicular calcium transient during calcium release from sarcoplasmic reticulum. Biochemistry 30:5230–5237
Irvine, R.F. 1990. “Quantal” Ca2+ release and the control of Ca2+ entry by inositol phosphates—a possible mechanism. FEBS Lett. 262:5–9
Jaffe, L.F. 1991. The path of calcium in cytosolic calcium oscillations: a unifying hypothesis. Proc. Natl. Acad. Sci. USA 88:9883–9887
Javaraman, T., Brillantes, A.M., Timerman, A.P., Fleischer, S., Erdjument-Bromage, H., Tempst, P., Marks, A.R. 1992. FK506 binding protein associated with the calcium release channel (ryanodine receptor). J. Biol. Chem. 267:9474–9477
Jean, T., Klee, C.B. 1986. Calcium modulation of inositol 1,4,5-trisphosphate-induced calcium release from neuroblastoma x glioma hybrid (NG108–15) microsomes. J. Biol. Chem. 261:16414–16420
Kalinoski, D.L., Aldinger, S.B., Boyle, A.G., Huque, T., Maracek, J.F., Prestwich, G.D., Restrepo, D. 1992. Characterization of a novel inositol 1,4,5-trisphosphate receptor in isolated olfactory neurones. Biochem. J. 281:449–456
Khan, A.A., Steiner, J.P., Snyder, S.H. 1992. Plasma membrane inositol 1,4,5-trisphosphate receptor of lymphocytes: selective enrichment in sialic acid and unique binding specificity. Proc. Natl. Acad. Sci. USA 89:2849–2853
Kume S., Muto, A., Aruga, J., Nakagawa, T., Michikawa, T., Furuichi, T., Nakade, S., Okano, H., Mikoshiba, K. 1993. The Xenopus IP3 receptor: structure, function and localization in oocytes and eggs. Cell 75:555–570
Lai, F.A., Meissner, G. 1989. The muscle ryanodine receptor and its intrinsic Ca2+ channel activity. J. Bioenerg. Biomembr. 21:227–246
Lee, H.C. 1993. Potentiation of calcium- and caffeine-induced calcium release by cyclic ADP ribose. J. Biol. Chem. 268:293–299
Lee, H.C., Aarhus, R., Graeff, R., Gurnack, M.E., Walseth, T.F. 1994. Cyclic ADP ribose activation of the ryanodine receptor is mediated by calmodulin. Nature 370:307–309
Loomis-Husselbee, J.W., Dawson, A.P. 1993. A steady-state mechanism can account for the properties of inositol 2,4,5-trisphosphate-stimulated Ca2+ release from permeabilized L1210 cells. Biochem. J. 289:861–866
Lytton, J., Nigam, S.R. 1992. Intracellular calcium: molecules and pools. Curr. Op. Cell. Biol. 4:220–226
Maranto, A.R. 1994. Primary structure, ligand binding, and localization of the human type 3 inositol 1,4,5-trisphosphate receptor expressed in intestinal epithelium. J. Biol. Chem. 269:1222–1230
Marshall, I.C.B., Taylor, C.W. 1993. Regulation of inositol 1,4,5-trisphosphate receptors. J. Exp. Biol. 184:161–182
Marshall, I.C.B., Taylor, C.W. 1993. Biphasic effects of cytosolic calcium on Ins(1,4,5)P3-stimulated Ca2+ mobilization in hepatocytes. J. Biol. Chem. 268:13214–13220
Marshall, I.C.B., Taylor, C.W. 1994. Two calcium-binding sites mediate the interconversion of liver inositol 1,4,5-trisphosphate receptors between three conformational states. Biochem. J. 301:591–598
McPherson, P.S., Campbell, K.P. 1993. The ryanodine receptor/Ca2+ release channel. J. Biol. Chem. 268:13765–13768
Meyer, T., Holowka, D., Stryer, L. 1988. Highly cooperative opening of calcium channels by inositol 1,4,5-trisphosphate. Science 240:653–656
Meyer, T., Stryer, L. 1990. Transient calcium release induced by successive increments of inositol 1,4,5-trisphosphate. Proc. Natl. Acad. Sci. USA 87:3841–3845
Michell, R.H. 1975. Inositol phospholipids and cell surface receptor function. Biochim. Biophys. Acta 415:81–147
Michikawa, T., Hamanaka, H., Otsu, H., Yamamoto, A., Miyawaki, A., Furuichi, T., Tashiro, Y., Mikoshiba, K. 1994. Transmembrane topology and sites of N-glycosylation of inositol 1,4,5-trisphosphate receptor. J. Biol. Chem. 269:9184–9189
Mignery, G.A., Johnston, P.A., Südhof, T.C. 1992. Mechanism of Ca2+ inhibition of inositol 1,4,5-trisphosphate (InsP3) binding to the cerebellum InsP3 receptor. J. Biol. Chem. 267:7450–7455
Mignery, G.A., Südhof, T.C. 1990. The ligand binding site and transduction mechanism in the inositol-1,4,5-trisphosphate receptor. EMBO J. 9:3893–3898
Mignery, G.A., Südhof, T.C., Takei, K., De Camilli, P. 1989. Putative receptor for inositol 1,4,5-trisphosphate similar to ryanodine receptor. Nature 342:192–195
Mikoshiba, K. 1993. Inositol 1,4,5-trisphosphate receptor. Trends Pharmacol. Sci 14:86–89
Miller, C. 1992. Hunting for the pore of voltage-gated channels. Curr. Biol. 2:573–575
Missiaen, L., De Smedt, H., Droogmans, G., Casteels, R. 1992. Ca2+ release induced by inositol 1,4,5-trisphosphate is a steadystate phenomenon controlled by luminal Ca2+ in permeabilized cells. Nature 357:599–602
Missiaen, L., De Smedt, H., Parys, J.B., Casteels, R. 1994. Coactivation of inositol trisphosphate-induced Ca2+ release by cytosolic Ca2+ is loading-dependent. J. Biol. Chem. 269:7238–7242
Missiaen, L., Taylor, C.W., Berridge, M.J. 1992. Luminal Ca2+ promoting spontaneous Ca2+ release from inositol trisphosphatesensitive stores of rat hepatocytes. J. Physiol. 455:623–640
Miyawaki, A., Furuichi, T., Maeda, N., Mikoshiba, K. 1990. Expressed cerebellar-type inositol 1,4,5-trisphosphate receptor, P400, has calcium release activity in a fibroblast L cell line. Neuron 5:11–18
Mourey, R.J., Verma, A., Supattapone. S., Snyder, S.H. 1990. Purification and characterization of the inositol 1,4,5-trisphosphate receptor protein from rat vas deferens. Biochem. J. 270: 383–389
Muallem, S., Pandol, S.J., Beeker, T.G. 1989. Hormone-evoked calcium release from intracellular stores is a quantal process. J. Biol. Chem. 264:205–212
Nahorski, S.R., Potter, B.V.L. 1989. Molecular recognition of inositol polyphosphates by intracellular receptors and metabolic enzymes. Trends Pharmacol. Sci. 10:139–144
Nakade, S., Rhee, S.K., Hamanaka, H., Mikoshiba, K. 1994. Cyclic AMP-dependent phosphorylation of an immunoaffinitypurified homotetrameric inositol 1,4,5-trisphosphate receptor (type 1) increases Ca2+ flux in reconstituted lipid vesicles. J. Biol. Chem. 269:6735–6742
Nakagawa. T., Okano, H., Furuichi, T., Aruga, J., Mikoshiba, K. 1991. The subtypes of the mouse inositol 1,4,5-trisphosphate receptor are expressed in tissue-specific and developmentally specific manner. Proc. Natl. Acad. Sci. USA 88:6244–6248
Nelson, T.E., Nelson, K.E. 1990. Intra- and extraluminal sarcoplasmic reticulum membrane regulatory sites for Ca2+-induced Ca2+ release. FEBS Lett. 263:292–294
Nunn, D.L., Taylor, C.W. 1992. Luminal Ca2+ increases the sensitivity of Ca2+ stores to inositol 1,4,5-trisphosphate. Mol. Pharmacol. 41:115–119
Oldershaw, K.A., Taylor, C.W. 1993. Luminal Ca2+ increases the affinity of inositol 1,4,5-trisphosphate for its receptor. Biochem. J. 292:631–633
Parys. J.B., Missiaen, L., De Smedt, H., Casteels, R. 1993. Loading dependence of inositol 1,4,5-trisphosphate-induced Ca2+ release in the clonal cell line A7r5. J. Biol. Chem. 268:25206–25212
Pietri, F., Hilly, M., Mauger, J-P. 1990. Calcium mediates the interconversion between two states of the liver inositol 1,4,5-trisphosphate receptor. J. Biol. Chem. 265:17478–17485
Putney, J.W., Jr., Bird, G.St.J. 1993. The inositol phosphatecalcium signalling system in nonexcitable cells. Endocr. Rev. 14:610–631
Rapp, P.E., Mees, A.I., Sparrow, C.T. 1981. Frequency encoded biochemical regulation is more accurate than amplitude dependent control. J. Theor. Biol. 90:531–544
Renard-Rooney, D.C., Hajnóczky, G., Seitz, M.B., Schneider, T.G., Thomas, A.P. 1993. Imaging of inositol 1,4,5-trisphosphate-induced Ca2+ fluxes in single permeabilized hepatocytes: demonstration of both quantal and nonquantal patterns of Ca2+ release. J. Biol. Chem. 268:23601–23610
Richardson, A., Taylor, C.W. 1993. Effects of Ca2+ chelators on purified inositol 1,4,5-trisphosphate (InsP3) receptors and InsP3-stimulated Ca2+ mobilization. J. Biol. Chem. 268:11528–11533
Rizzuto, R., Brini, M., Murgia, M., Pozzan, T. 1993. Microdomains with high Ca2+ close to IP3-sensitive channels that are sensed by neighbouring mitochondria. Science 262:744–747
Rooney, T.A., Thomas, A.P. 1993. Intracellular calcium waves generated by Ins(1,4,5)P3-dependent mechanisms. Cell Calcium 14:674–690
Rossier, M.F., Bird, G.St.J., Putney, J.W., Jr. 1991. Subcellular distribution of the calcium-storing inositol 1,4,5-trisphosphatesensitive organelle in rat liver. Possible linkage to the plasma membrane through actin microfilaments. Biochem. J. 274:643–650
Sayers, L.G., Brown, G.R., Michell, R.H., Michelangeli, F. 1993. The effects of thimerosal on calcium uptake and inositol 1,4,5-trisphosphate-induced calcium release in cerebellar microsomes. Biochem. J. 289:883–887
Shuttleworth, T.J. 1992. Ca2+release from inositol trisphosphatesensitive stores is not modulated by intraluminal [Ca2+]. J. Biol. Chem. 267:3573–3576
Sitsapesan, R., Williams, A.J. 1994. Regulation of the gating of the sheep cardiac sarcoplasmic reticulum Ca2+-release channel by luminal Ca2+. J. Membrane Biol. 137:215–226
Smith, J.S., Imagawa, T., Jianje, M., Fill, M, Campbell, K.P., Coronado, R. 1988. Purified ryanodine receptor from rabbit skeletal muscle is the calcium-release channel of sarcoplasmic reticulum. Biophys. J. 92:1–26
Sorrentino, V., Volpe. P. 1993. Ryanodine receptors: how many, where, and why? Trends Pharmacol. Sci. 14:98–103
Spät, A., Bradford, P.G., McKinney, J.S., Rubin, R.P., Putney, J.W., Jr. 1986. A saturable receptor for 32P-inositol- 1,4,5-trisphosphate in hepatocytes and neutrophils. Nature 319:514–516
Stern, M.D. 1992. Buffering of calcium in the vicinity of a channel pore. Cell Calcium 13:183–192
Streb, H., Irvine, R.F., Berridge, M.J., Schulz, I. 1983. Release of Ca2+ from a nonmitochondrial store of pancreatic acinar cells by inositol-1,4,5-trisphosphate. Nature 306:67–69
Suematsu, E., Hirata, M., Hashimoto, T., Kuriyama, H. 1984. Inositol 1,4,5-trisphosphate releases Ca2+ from intracellular store sites in skinned single cells of porcine coronary artery. Biochem. Biophys. Res. Commun. 120:481–485
Supattapone, S., Worley, P.F., Baraban, J.M., Snyder, S.H. 1988. Solubilization, purification, and characterization of an inositol trisphosphate receptor. J. Biol. Chem. 263:1530–1534
Suárez-Isla, B.A., Alcayaga, C., Marengo, J.J., Bull, R. 1991. Activation of inositol trisphosphate-sensitive Ca2+ channels of sarcoplasmic reticulum from frog skeletal muscle. J. Physiol. 441:575–591
Südhof, T.C., Newton, C.L., Archer, B.T. III, Ushkaryov, Y.A., Mignery, G.A. 1991. Structure of a novel InsP3 receptor. EMBO J. 10:3199–3206
Takeshima, H., Nishi, M., Iwabe, N., Miyata, T., Hoso, T.ya., Masai, I., Hotta, Y. 1994. Isolation and characterization of a gene for a ryanodine receptor/calcium release channel in Drosophila melanogaster. FEBS Lett. 337:81–87
Taylor, C.W. 1992. Kinetics of inositol 1,4,5-trisphosphatestimulated Ca2+ mobilization. Adv. Second Mess. Phos. Res. 26:109–142
Taylor, C.W., Marshall, I.C.B. 1992. Calcium and inositol 1,4,5-trisphosphate receptors: a complex relationship. Trends Biochem. Sci. 17:403–407
Taylor, C.W., Richardson, A. Structure and function of inositol trisphosphate receptors. In: Intracellular Messengers, C.W. Taylor, editor. Pergamon Oxford 1993, p, 199–254
Tinker, A., Williams, A.J. 1992. Divalent cation conduction in the ryanodine receptor channel of sheep cardiac muscle sarcoplasmic reticulum. J. Gen. Physiol. 100:479–493
Tsien, R.W., Tsien, R.Y. 1990. Calcium channels, stores and oscillations. Annu. Rev. Cell Biol. 6:715–760
Wang, J., Best, P.M. 1992. Inactivation of the sarcoplasmic reticulum calcium channel by protein kinase. Nature 359:739–741
Watras, J., Bezprozvanny, I., Ehrlich, B.E. 1991. Inositol 1,4,5-trisphosphate-gated channels in cerebellum: presence of multiple subconductance states. J. Neurosci. 11:3239–3249
Yamamoto-Hino, M., Sugiyama, T., Hikichi, K., Mattei, M.G., Hasegawa, K., Sekine, S., Sakurada, K., Miyawaki, A., Furuichi, T., Hasegawa, M., Mikoshiba, K. (1993). Cloning and characterization of human type 2 and type 3 inositol 1,4,5-trisphosphate receptors. Receptors and Channels (in press)
Yao, T., Parker, I. 1993. Inositol trisphosphate-mediated Ca2+ influx into Xenopus oocytes triggers Ca2+ liberation from intracellular stores. J. Physiol. 468:275–296
Yao, Y., Parker, I. 1994. Ca2+ influx modulation of temporal and spatial patterns of inositol trisphosphate-mediated Ca2+ liberation in Xenopus oocytes. J. Physiol. 476:17–28
Yoshikawa, S., Tanimura, T., Miyawaki, A., Nakamura, M., Yuzaki, M., Furuichi, T., Mikoshiba, K. 1992. Molecular cloning of and characterization of the inositol 1,4,5-trisphosphate receptor in Drosophila melanogaster. J. Biol. Chem. 267:16613–16619
Zhang, B-X., Zhao, H., Muallem, S. 1993. Ca2+-dependent kinase and phosphatase control inositol 1,4,5-trisphosphate-mediated Ca2+ release. J. Biol. Chem. 268:10997–11001
Zhao, H., Muallem, S. 1990. Inhibition of inositol 1,4,5-trisphosphate-mediated Ca2+ release by Ca2+ in cells from peripheral tissues. J. Biol. Chem. 265:21419–21422
Author information
Authors and Affiliations
Additional information
Work from the authors' laboratory is supported by the Wellcome Trust, and the Medical, and Agricultural and Food Research Councils. CWT is a Lister Institute Research Fellow.
Rights and permissions
About this article
Cite this article
Taylor, C.W., Traynor, D. Calcium and inositol trisphosphate receptors. J. Membarin Biol. 145, 109–118 (1995). https://doi.org/10.1007/BF00237369
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF00237369