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. 2000 Jan 15;345(Pt 2):357–363.

Ca2+-calmodulin inhibits Ca2+ release mediated by type-1, -2 and -3 inositol trisphosphate receptors.

C E Adkins 1, S A Morris 1, H De Smedt 1, I Sienaert 1, K Török 1, C W Taylor 1
PMCID: PMC1220765  PMID: 10620513

Abstract

InsP(3) binding to type-1, but not type-3, InsP(3) receptors is inhibited by calmodulin in a Ca(2+)-independent fashion [Cardy and Taylor (1998) Biochem. J. 334, 447-455], and Ca(2+) mobilization by type-1 InsP(3) receptors of cerebellum is inhibited by calmodulin [Patel, Morris, Adkins, O'Beirne and Taylor (1997) Proc. Natl. Acad. Sci. U.S.A. 94, 11627-11632]. Using cell types expressing predominantly type-1, -2 or -3 InsP(3) receptors, we show that InsP(3)-evoked Ca(2+) mobilization from each is similarly inhibited by calmodulin. In SH-SY5Y cells, which express largely type-1 receptors, calmodulin (IC(50) approximately 15 microM) inhibited InsP(3)-evoked Ca(2+) release only in the presence of Ca(2+). The inhibition was unaffected by calcineurin inhibitors. The effect of calmodulin did not result from enhanced metabolism of InsP(3) because calmodulin also decreased the sensitivity of the Ca(2+) stores to adenophostin A, a non-metabolizable InsP(3)-receptor agonist. Protein kinase A-catalysed phosphorylation of type-1 InsP(3) receptors was unaffected by Ca(2+)-calmodulin. Using a scintillation proximity assay to measure (125)I-calmodulin binding to glutathione S-transferase-fusion proteins, we identified two regions of the type-1 InsP(3) receptor (cyt1, residues -6 to 159; and cyt11, residues 1499-1649) that bound (125)I-calmodulin. The higher-affinity site (cyt11) was also photoaffinity labelled with N-hydroxysuccinimidyl-4-azidobenzoate (HSAB)-calmodulin. We speculate that Ca(2+)-independent binding of calmodulin to a site within the first 159 residues of the type-1 InsP(3) receptor inhibits InsP(3) binding and may thereby regulate the kinetics of Ca(2+) release. Ca(2+)-dependent inhibition of Ca(2+) release by calmodulin is mediated by a different site: it may reside on an accessory protein that associates with all three receptor subtypes, or Ca(2+)-calmodulin binding to a site lying between residues 1499 and 1649 of the type-1 receptor may inhibit Ca(2+) release from any tetrameric receptor that includes a type-1 subunit.

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Selected References

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  1. Bredt D. S., Ferris C. D., Snyder S. H. Nitric oxide synthase regulatory sites. Phosphorylation by cyclic AMP-dependent protein kinase, protein kinase C, and calcium/calmodulin protein kinase; identification of flavin and calmodulin binding sites. J Biol Chem. 1992 Jun 5;267(16):10976–10981. [PubMed] [Google Scholar]
  2. Cameron A. M., Steiner J. P., Roskams A. J., Ali S. M., Ronnett G. V., Snyder S. H. Calcineurin associated with the inositol 1,4,5-trisphosphate receptor-FKBP12 complex modulates Ca2+ flux. Cell. 1995 Nov 3;83(3):463–472. doi: 10.1016/0092-8674(95)90124-8. [DOI] [PubMed] [Google Scholar]
  3. Carafoli E. The Ca2+ pump of the plasma membrane. J Biol Chem. 1992 Feb 5;267(4):2115–2118. [PubMed] [Google Scholar]
  4. Cardy T. J., Taylor C. W. A novel role for calmodulin: Ca2+-independent inhibition of type-1 inositol trisphosphate receptors. Biochem J. 1998 Sep 1;334(Pt 2):447–455. doi: 10.1042/bj3340447. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cardy T. J., Traynor D., Taylor C. W. Differential regulation of types-1 and -3 inositol trisphosphate receptors by cytosolic Ca2+. Biochem J. 1997 Dec 15;328(Pt 3):785–793. doi: 10.1042/bj3280785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chu A., Sumbilla C., Inesi G., Jay S. D., Campbell K. P. Specific association of calmodulin-dependent protein kinase and related substrates with the junctional sarcoplasmic reticulum of skeletal muscle. Biochemistry. 1990 Jun 26;29(25):5899–5905. doi: 10.1021/bi00477a003. [DOI] [PubMed] [Google Scholar]
  7. De Smedt H., Missiaen L., Parys J. B., Henning R. H., Sienaert I., Vanlingen S., Gijsens A., Himpens B., Casteels R. Isoform diversity of the inositol trisphosphate receptor in cell types of mouse origin. Biochem J. 1997 Mar 1;322(Pt 2):575–583. doi: 10.1042/bj3220575. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Dong Y., Kunze D. L., Vaca L., Schilling W. P. Ins(1,4,5)P3 activates Drosophila cation channel Trpl in recombinant baculovirus-infected Sf9 insect cells. Am J Physiol. 1995 Nov;269(5 Pt 1):C1332–C1339. doi: 10.1152/ajpcell.1995.269.5.C1332. [DOI] [PubMed] [Google Scholar]
  9. Edwardson J. M., An S., Jahn R. The secretory granule protein syncollin binds to syntaxin in a Ca2(+)-sensitive manner. Cell. 1997 Jul 25;90(2):325–333. doi: 10.1016/s0092-8674(00)80340-2. [DOI] [PubMed] [Google Scholar]
  10. Ehlers M. D., Zhang S., Bernhadt J. P., Huganir R. L. Inactivation of NMDA receptors by direct interaction of calmodulin with the NR1 subunit. Cell. 1996 Mar 8;84(5):745–755. doi: 10.1016/s0092-8674(00)81052-1. [DOI] [PubMed] [Google Scholar]
  11. Ferris C. D., Huganir R. L., Bredt D. S., Cameron A. M., Snyder S. H. Inositol trisphosphate receptor: phosphorylation by protein kinase C and calcium calmodulin-dependent protein kinases in reconstituted lipid vesicles. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2232–2235. doi: 10.1073/pnas.88.6.2232. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gnegy M. E. Calmodulin in neurotransmitter and hormone action. Annu Rev Pharmacol Toxicol. 1993;33:45–70. doi: 10.1146/annurev.pa.33.040193.000401. [DOI] [PubMed] [Google Scholar]
  13. Kakiuchi S., Yasuda S., Yamazaki R., Teshima Y., Kanda K., Kakiuchi R., Sobue K. Quantitative determinations of calmodulin in the supernatant and particulate fractions of mammalian tissues. J Biochem. 1982 Oct;92(4):1041–1048. doi: 10.1093/oxfordjournals.jbchem.a134019. [DOI] [PubMed] [Google Scholar]
  14. Lan L., Bawden M. J., Auld A. M., Barritt G. J. Expression of Drosophila trpl cRNA in Xenopus laevis oocytes leads to the appearance of a Ca2+ channel activated by Ca2+ and calmodulin, and by guanosine 5'[gamma-thio]triphosphate. Biochem J. 1996 Jun 15;316(Pt 3):793–803. doi: 10.1042/bj3160793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lee A., Wong S. T., Gallagher D., Li B., Storm D. R., Scheuer T., Catterall W. A. Ca2+/calmodulin binds to and modulates P/Q-type calcium channels. Nature. 1999 May 13;399(6732):155–159. doi: 10.1038/20194. [DOI] [PubMed] [Google Scholar]
  16. Lee H. C., Aarhus R., Graeff R. M. Sensitization of calcium-induced calcium release by cyclic ADP-ribose and calmodulin. J Biol Chem. 1995 Apr 21;270(16):9060–9066. doi: 10.1074/jbc.270.16.9060. [DOI] [PubMed] [Google Scholar]
  17. Liu M., Chen T. Y., Ahamed B., Li J., Yau K. W. Calcium-calmodulin modulation of the olfactory cyclic nucleotide-gated cation channel. Science. 1994 Nov 25;266(5189):1348–1354. doi: 10.1126/science.266.5189.1348. [DOI] [PubMed] [Google Scholar]
  18. Maeda N., Kawasaki T., Nakade S., Yokota N., Taguchi T., Kasai M., Mikoshiba K. Structural and functional characterization of inositol 1,4,5-trisphosphate receptor channel from mouse cerebellum. J Biol Chem. 1991 Jan 15;266(2):1109–1116. [PubMed] [Google Scholar]
  19. Marchant J. S., Beecroft M. D., Riley A. M., Jenkins D. J., Marwood R. D., Taylor C. W., Potter B. V. Disaccharide polyphosphates based upon adenophostin A activate hepatic D-myo-inositol 1,4,5-trisphosphate receptors. Biochemistry. 1997 Oct 21;36(42):12780–12790. doi: 10.1021/bi971397v. [DOI] [PubMed] [Google Scholar]
  20. Marchant J. S., Taylor C. W. Rapid activation and partial inactivation of inositol trisphosphate receptors by inositol trisphosphate. Biochemistry. 1998 Aug 18;37(33):11524–11533. doi: 10.1021/bi980808k. [DOI] [PubMed] [Google Scholar]
  21. Means A. R., Dedman J. R. Calmodulin--an intracellular calcium receptor. Nature. 1980 May 8;285(5760):73–77. doi: 10.1038/285073a0. [DOI] [PubMed] [Google Scholar]
  22. Michikawa T., Hirota J., Kawano S., Hiraoka M., Yamada M., Furuichi T., Mikoshiba K. Calmodulin mediates calcium-dependent inactivation of the cerebellar type 1 inositol 1,4,5-trisphosphate receptor. Neuron. 1999 Aug;23(4):799–808. doi: 10.1016/s0896-6273(01)80037-4. [DOI] [PubMed] [Google Scholar]
  23. Missiaen L., Parys J. B., Weidema A. F., Sipma H., Vanlingen S., De Smet P., Callewaert G., De Smedt H. The bell-shaped Ca2+ dependence of the inositol 1,4, 5-trisphosphate-induced Ca2+ release is modulated by Ca2+/calmodulin. J Biol Chem. 1999 May 14;274(20):13748–13751. doi: 10.1074/jbc.274.20.13748. [DOI] [PubMed] [Google Scholar]
  24. Nunn D. L., Taylor C. W. Luminal Ca2+ increases the sensitivity of Ca2+ stores to inositol 1,4,5-trisphosphate. Mol Pharmacol. 1992 Jan;41(1):115–119. [PubMed] [Google Scholar]
  25. Patel S., Morris S. A., Adkins C. E., O'Beirne G., Taylor C. W. Ca2+-independent inhibition of inositol trisphosphate receptors by calmodulin: redistribution of calmodulin as a possible means of regulating Ca2+ mobilization. Proc Natl Acad Sci U S A. 1997 Oct 14;94(21):11627–11632. doi: 10.1073/pnas.94.21.11627. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Phillips A. M., Bull A., Kelly L. E. Identification of a Drosophila gene encoding a calmodulin-binding protein with homology to the trp phototransduction gene. Neuron. 1992 Apr;8(4):631–642. doi: 10.1016/0896-6273(92)90085-r. [DOI] [PubMed] [Google Scholar]
  27. Richardson A., Taylor C. W. Effects of Ca2+ chelators on purified inositol 1,4,5-trisphosphate (InsP3) receptors and InsP3-stimulated Ca2+ mobilization. J Biol Chem. 1993 Jun 5;268(16):11528–11533. [PubMed] [Google Scholar]
  28. Seiler S., Wegener A. D., Whang D. D., Hathaway D. R., Jones L. R. High molecular weight proteins in cardiac and skeletal muscle junctional sarcoplasmic reticulum vesicles bind calmodulin, are phosphorylated, and are degraded by Ca2+-activated protease. J Biol Chem. 1984 Jul 10;259(13):8550–8557. [PubMed] [Google Scholar]
  29. Sienaert I., Missiaen L., De Smedt H., Parys J. B., Sipma H., Casteels R. Molecular and functional evidence for multiple Ca2+-binding domains in the type 1 inositol 1,4,5-trisphosphate receptor. J Biol Chem. 1997 Oct 10;272(41):25899–25906. doi: 10.1074/jbc.272.41.25899. [DOI] [PubMed] [Google Scholar]
  30. Sipma H., De Smet P., Sienaert I., Vanlingen S., Missiaen L., Parys J. B., De Smedt H. Modulation of inositol 1,4,5-trisphosphate binding to the recombinant ligand-binding site of the type-1 inositol 1,4, 5-trisphosphate receptor by Ca2+ and calmodulin. J Biol Chem. 1999 Apr 23;274(17):12157–12162. doi: 10.1074/jbc.274.17.12157. [DOI] [PubMed] [Google Scholar]
  31. Swatton J. E., Morris S. A., Cardy T. J., Taylor C. W. Type 3 inositol trisphosphate receptors in RINm5F cells are biphasically regulated by cytosolic Ca2+ and mediate quantal Ca2+ mobilization. Biochem J. 1999 Nov 15;344(Pt 1):55–60. [PMC free article] [PubMed] [Google Scholar]
  32. Takahashi S., Kinoshita T., Takahashi M. Adenophostins A and B: potent agonists of inositol-1,4,5-trisphosphate receptor produced by Penicillium brevicompactum. Structure elucidation. J Antibiot (Tokyo) 1994 Jan;47(1):95–100. doi: 10.7164/antibiotics.47.95. [DOI] [PubMed] [Google Scholar]
  33. 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]
  34. Török K., Trentham D. R. Mechanism of 2-chloro-(epsilon-amino-Lys75)-[6-[4-(N,N- diethylamino)phenyl]-1,3,5-triazin-4-yl]calmodulin interactions with smooth muscle myosin light chain kinase and derived peptides. Biochemistry. 1994 Nov 1;33(43):12807–12820. doi: 10.1021/bi00209a012. [DOI] [PubMed] [Google Scholar]
  35. Wang J., Best P. M. Inactivation of the sarcoplasmic reticulum calcium channel by protein kinase. Nature. 1992 Oct 22;359(6397):739–741. doi: 10.1038/359739a0. [DOI] [PubMed] [Google Scholar]
  36. 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]
  37. Wojcikiewicz R. J., Nahorski S. R. Chronic muscarinic stimulation of SH-SY5Y neuroblastoma cells suppresses inositol 1,4,5-trisphosphate action. Parallel inhibition of inositol 1,4,5-trisphosphate-induced Ca2+ mobilization and inositol 1,4,5-trisphosphate binding. J Biol Chem. 1991 Nov 25;266(33):22234–22241. [PubMed] [Google Scholar]
  38. Yakel J. L. Calcineurin regulation of synaptic function: from ion channels to transmitter release and gene transcription. Trends Pharmacol Sci. 1997 Apr;18(4):124–134. doi: 10.1016/s0165-6147(97)01046-8. [DOI] [PubMed] [Google Scholar]
  39. Yamada M., Miyawaki A., Saito K., Nakajima T., Yamamoto-Hino M., Ryo Y., Furuichi T., Mikoshiba K. The calmodulin-binding domain in the mouse type 1 inositol 1,4,5-trisphosphate receptor. Biochem J. 1995 May 15;308(Pt 1):83–88. doi: 10.1042/bj3080083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Yoshikawa F., Iwasaki H., Michikawa T., Furuichi T., Mikoshiba K. Trypsinized cerebellar inositol 1,4,5-trisphosphate receptor. Structural and functional coupling of cleaved ligand binding and channel domains. J Biol Chem. 1999 Jan 1;274(1):316–327. doi: 10.1074/jbc.274.1.316. [DOI] [PubMed] [Google Scholar]
  41. Yoshikawa F., Uchiyama T., Iwasaki H., Tomomori-Satoh C., Tanaka T., Furuichi T., Mikoshiba K. High efficient expression of the functional ligand binding site of the inositol 1,4,5-triphosphate receptor in Escherichia coli. Biochem Biophys Res Commun. 1999 Apr 21;257(3):792–797. doi: 10.1006/bbrc.1999.0498. [DOI] [PubMed] [Google Scholar]
  42. Zühlke R. D., Pitt G. S., Deisseroth K., Tsien R. W., Reuter H. Calmodulin supports both inactivation and facilitation of L-type calcium channels. Nature. 1999 May 13;399(6732):159–162. doi: 10.1038/20200. [DOI] [PubMed] [Google Scholar]

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