Skip to main content
Log in

Characterization of inositolpolyphosphate binding to myocardial membranes

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

Although it is well-accepted that the phosphatidylinositol signalling transduction pathway, producing inositol-1,4,5-P3 (InsP3) and inositol-1,3,4,5-P4 (InsP4) as second messengers, functions in heart muscle, virtually nothing is known about the roles of the higher inositol polyphosphates such as inositolhexakisphosphate (InsP6). This study demonstrates that InSP6 has the ability to bind intracellularly, with different binding characteristics, to different myocardial membranes. Binding to purified sarcoplasmic reticulum (SR) membranes, purified sarcolemmal (SL) membranes as well as to viable mitochondria were characterized. Binding to all these membranes display high as well as low affinity binding sites, with differing affinities. Kd values of binding to SR were 32 and 383 nM, to SL 61 and 1312 nM, while those of mitochondrial binding were 230 and 2200 nM respectively.

InsP4 binding was also investigated and displayed the following characteristics: to SR, one low affinity binding site (Kd = 203 nM) and to SL, a high as well as a low affinity binding site with Kd values of 41 and 2075 nM respectively. Presence of InsP3, the second messenger for SR calcium release, at concentrations of 1 nM, elevated the binding of InsP4 to SR and SL by a mean of 30% and 20% respectively.

Fractionation of SR and SL membranes on sucrose density gradients, after solubilization with CHAPS, indicated that InsP6 bound to two separate protein peaks in both these membranes, while InsP4 bound to only one. In SR membranes, InsP4 bound preferentially to a protein separating at high sucrose density while it bound to a protein separating at low sucrose density in SL membranes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Berridge MJ: Inositol trisphosphate and calcium signalling. Nature 361: 315–325,1993

    Article  CAS  PubMed  Google Scholar 

  2. Putney JWJ Jr, Bird GStJ: The inositol phosphate-calcium signalling system in nonexcitable cells. Endocrine Rev 14: 510–631, 1993

    Google Scholar 

  3. Berridge MJ, Irvine RF: Inositol phosphates and cell signalling. Nature 341: 197–205, 1989

    Google Scholar 

  4. Menniti FS, Oliver KG, Nogimori K, Obie JF, Shears SB, Putney JW Jr: Origins of myo-Inositol tetrakisphosphates in agonist-stimulated rat pancreatoma cells. Stimulation by bombesin of myo-Inositol 1,3,4,5,6-pentakis-phosphate breakdown to myo-Inositol 3,4,5,6tetrakisphosphate. J Biol Chem 265: 11167–11176, 1990

    Google Scholar 

  5. Oliver KG, Putney JW, Obie JF, Shears SB: The interconversion of inositol 1,3,4,5,6-pentakisphosphate and inositol tetrakisphosphate in AR4–21 cells. J Biol Chem 267: 21528–21534, 1992

    Google Scholar 

  6. Menniti FS, Miller RN, Putney JW Jr, Shears SB: Turnover of inositol polyphosphate pyrophosphates in pancreatoma cells. J Biol Chem 268: 3850–3856,1993

    Google Scholar 

  7. Sasakawa N, Nakaki T, Kashima R, Kanba S, Kato R: Stimulus induced accumulation of inositol tetrakis-, pentakis- and hexakisphosphates in NIE-115 Neuroblastoma cells. J Neurochem 58: 2116–2123, 1992

    Google Scholar 

  8. Vallejo M, Jackson T, Lightman S, Hanley MR: Occurrence and extracellular actions of inositol pentakis- and hexakisphosphates in mammalian brain. Nature 330: 656–658, 1987

    Google Scholar 

  9. Nicoletti F, Bruno V, Fiore L, Cavallaro S, Canonico PL: Inositol hexakisphosphate (phytic acid) enhances Ca2+ influx and D-[3H] aspartate release in cultured cerebellar neurons. J Neurochem 53: 1026–1030,1989

    Google Scholar 

  10. Sortino MA, Nicoletti F, Canonico PL: Inositolhexakisphosphate stimulates 45Cal4uptake in anterior pituitary cells in culture. Eur J Pharmacol 189:115–118,1990

    Google Scholar 

  11. Regunathan S, Reis DJ, Wahlestedt C: Specific binding of inositol hexakisphosphate (phytic acid) to adrenal chromaffm cell membranes and effects on calcium-dependent catecholamine release. Biochem Pharmacol 43: 1331–1336, 1992

    Google Scholar 

  12. Scholz J, Troll U, Sandig P, Schmitz W Scholz H, SchulteAm Esch J: Existence and alpha, -adrenergic stimulation of inositol polyphosphates in mammalian heart. Mol Pharm 42: 134–140, 1992

    Google Scholar 

  13. Rao PS, Lui X, Das DK, Weinstein GS, Tyras DH: Protection of ischaemic heart from reperfusion injury by myo-Inositol hexaphosphate, a natural anti-oxidant. Ann Thorac Surg 52: 908–912, 1991

    Google Scholar 

  14. Hawkins PT, Reynolds DJM, Poyner DR, Hanley MR: Identification of 2 novel inositol phosphate recognition site: Specific [3H]Inositol hexakisphosphate binding to brain regions and cerebellar membranes. Biochem Biophys Res Commun 167: 819–827, 1990

    Google Scholar 

  15. Theibert AB, Esteves VA, Ferris CD, Danoff SIC, Barrow RK, Prestwich GD, Snyder SH: Inositol 1,3,4,5-tetrakisphosphate and Inositol hexakisphosphate receptor proteins: Isolation and characterization from rat brain. Proc Natl Acad Sci 88: 3165–3169, 1991

    Google Scholar 

  16. Timerman AP, Mayrleitner MM, Lukas TJ, Chadwick CC, Saito A, Watterson DM, Schindler H, Fleischer S: Inositol polyphosphate receptor and clathrin assembly protein AP-2 are related proteins that form potassium-selective ion channels in planar lipid bilayers. Proc Soc Natl Acad Sci 89: 8976–8980, 1992

    Google Scholar 

  17. Voglmaier SM, Keen JH, Murphy J-E, Ferris CD, Prestwich GD, Snyder SH, Theibert AB: Inositol hexakisphosphate receptor identified as the clathrin assembly protein AP-2. Biochem Biophys Res Commun 187: 158–163,1992

    Google Scholar 

  18. Poyner DR, Cooke F, Hanley MR, Reynolds JM, Hawkins PT: Characterization of metal ion-induced [3H] inositol hexakisphosphate binding to rat cerebellar membranes. J Biol Chem 268: 1032–1038, 1993

    Google Scholar 

  19. Kijima Y, Fleischer, S: Two types of Inositol trisphosphate binding in cardiac microsomes. Biochem Biophys Res Commun 189: 728–735, 1992

    Google Scholar 

  20. Theibert AB, Supattapone S, Worley PF, Baraban JM, Meek JL, Snyder SH: Demonstration of inositol 1,3,4,5-tetrakispbosphate receptor binding. Biochem Biophys Res Comm 148: 1283–1289,1987

    Google Scholar 

  21. Sordahl CA, Johnson C, Blailock ZR, Schwartz A: The mitochondrion. Methods of Pharmacology 1: 247–286, 1971

    Google Scholar 

  22. Feher JJ, Davis, MD: Isolation of rat cardiac sarcoplasmic reticulum with improved CO2+ uptake and ryanodine binding. J Mol Cell Cardiol 23:249–258,1991

    Google Scholar 

  23. Philipson DK, Bets DM, Nishimoto AY The role of phospholipids in the Ca2+ binding of isolated cardiac sarcolemma. J Mol Cell Cardiol 12:1159–1173,1980

    Google Scholar 

  24. Venter H, Genade S, Mouton R, Huisamen B, Harper I, Lochner A: Myocardial membrane cholesterol: Effects of ischaemia. J Mol Cell Cardiol 23: 1271–1286, 1991

    Google Scholar 

  25. Wiid IJF, Huisamen B: An inexpensive approach to ultracentrifugation of small volume suspensions. BioTechniques 14: 564, 1993

    Google Scholar 

  26. Lowry AO, Rosenbrough NJ, Farr AL, Randall RJ: Protein with the folin phenol reagent. J Biol Chem 193: 265–275, 1951

    CAS  PubMed  Google Scholar 

  27. Kaplan RS, Pedersen PL: Determination of microgram quantities of protein in the presence of milligram levels of lipid with amido black 10B. Analyt Biochem 150: 97–104, 1985

    Google Scholar 

  28. Nicoletti F, Bruno V, Cavallaro S, Copani A, Sortino WA, Canonico PL: Specific binding sites for inositolhexakisphosphate in brain and anterior pituitary Mol Pharmacol 37: 689–693, 1990

    Google Scholar 

  29. Chadwick CC, Timerman AP, Saito A, Mayrleitner M, Schindler, H, Fleischer S: Structural and functional characterization of an inositol polyphosphate receptor from cerebellum. J Biol Chem 267: 3473–3481, 1992

    Google Scholar 

  30. Irvine RF: Inositol tetrakisphosphate as a second messenger: confusions, contradictions, and a potential resolution. BioEssays 13: 419–427

  31. Irvine RF, Cullen PJ: Will the real IP4 receptor please stand up? Current Biol 3: 540–543, 1993

    Google Scholar 

  32. Huisamen B, Opie LH, Lochner A: Demonstration of a specific [3H]Ins(1,4,5)P3 binding site in rat heart sarcoplasmic reticulum. J Mol Cell Cardiol 26: 341–349, 1994

    Google Scholar 

  33. Quist EE, Foresman BhH, Vasan R, Quist CW: Inositol tetrakisphosphate stimulates a novel ATP-independent Ca2+ uptake mechanism in cardiac junctional sarcoplasmic reticulum. Biochem Biophys Res Commun 204: 69–75, 1994

    Google Scholar 

  34. Klotz IM: Numbers of receptor sites from Scatchard graphs: facts and fantasies. Science 217: 1247–1249, 1982

    Google Scholar 

  35. Mayrleitner M, Schafer R, Fleischer S: IP3 receptor purified from liver plasma membrane is an (1,4,5)IP3 activated and (1,3,4,5)IP4 inhibited calcium permeable ion channel. Cell Calcium 17: 141–153, 1995

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Huisamen, B., Ellis, E., van Dyk, M. et al. Characterization of inositolpolyphosphate binding to myocardial membranes. Mol Cell Biochem 162, 1–9 (1996). https://doi.org/10.1007/BF00250989

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00250989

Key words

Navigation