Metabolism - Clinical and Experimental
Volume 44, Issue 7 , Pages 865-868 , July 1995

Inositol phosphates modulate human red blood cell Ca2+—adenosine triphosphatase activity in vitro by a guanine nucleotide regulatory protein

  • Faith B. Davis

      Affiliations

    • Division of Molecular and Cellular Medicine, Department of Medicine, Albany Medical College, Albany, USA
    • Stratton Department of Veterans Affairs Medical Center, Albany, USA
    • Department of Medicine, State University of New York at Buffalo School of Medicine and Biomedical Sciences, Buffalo, NY, USA
  • ,
  • Paul J. Davis

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Paul J. Davis, MD, Professor of Medicine, Department of Medicine A-57, Albany Medical College, Albany, NY 12208.
    • Division of Molecular and Cellular Medicine, Department of Medicine, Albany Medical College, Albany, USA
    • Stratton Department of Veterans Affairs Medical Center, Albany, USA
    • Department of Medicine, State University of New York at Buffalo School of Medicine and Biomedical Sciences, Buffalo, NY, USA
  • ,
  • Susan D. Blas

      Affiliations

    • Division of Molecular and Cellular Medicine, Department of Medicine, Albany Medical College, Albany, USA
    • Stratton Department of Veterans Affairs Medical Center, Albany, USA
    • Department of Medicine, State University of New York at Buffalo School of Medicine and Biomedical Sciences, Buffalo, NY, USA
  • ,
  • Denise Z. Gombas

      Affiliations

    • Division of Molecular and Cellular Medicine, Department of Medicine, Albany Medical College, Albany, USA
    • Stratton Department of Veterans Affairs Medical Center, Albany, USA
    • Department of Medicine, State University of New York at Buffalo School of Medicine and Biomedical Sciences, Buffalo, NY, USA

Received 7 February 1994 ,Accepted 9 November 1994.

References 

  1. Scharff O. Calmodulin and its role in cellular activation. Cell Calcium. 1981;2:1–27
  2. James P, Maeda M, Fischer R, et al.  Identification and primary structure of a calmodulin binding domain of the Ca2+ pump of human erythrocytes. J Biol Chem. 1988;263:2905–2910
  3. Niggli V, Adunyah ES, Carafoli E. Acidic phospholipids, unsaturated fatty acids, and limited proteolysis mimic the effect of calmodulin on the purified erythrocyte Ca2+-ATPase. J Biol Chem. 1981;256:8588–8592
  4. Davis FB, Davis PJ, Blas SD, et al.  Action of long-chain fatty acids in vitro on Ca2+-stimulatable, Mg2+-dependent ATPase activity in human red cell membranes. Biochem J. 1987;248:511–516
  5. Davis FB, Davis PJ, Nat G, et al.  The effect of in vivo glucose administration on human erythrocyte Ca2+-ATPase activity and on enzyme responsiveness in vitro to thyroid hormone and calmodulin. Diabetes. 1985;34:639–646
  6. Deziel MR, Safeer RS, Blas SD, et al.  Hexose-specific inhibition in vitro of human red cell Ca2+-ATPase activity. Biochim Biopbys Acta. 1992;1110:119–122
  7. Davis FB, Davis PJ, Lawrence WD, et al.  Specific inositol phosphates inhibit basal and calmodulin-stimulated Ca2+-ATPase activity in human erythrocyte membranes in vitro and inhibit binding of calmodulin to membranes. FASEB J. 1991;5:2992–2995
  8. Kuno N, Gardner P. Ion channels activated by inositol 1,4,5-trisphosphate in plasma membrane of human T-lymphocytes. Nature. 1987;326:301–304
  9. Penner R, Matthews G, Neher E. Regulation of calcium influx by second messengers in rat mast cells. Nature. 1988;334:499–504
  10. Mayr GW. Inositol 1,4-bisphosphate is an allosteric activator of muscle-type 6-phospho-fructo-1-kinase. Biochem J. 1989;259:463–470
  11. Berridge MJ. Temporal aspects of calcium signalling. In:  Nishizuka Y,  Endo M,  Tanaka C editor. The Biology and Medicine of Signal Transduction. New York, NY: Raven; 1990;p. 108–114
  12. Davis FB, Moffett MJ, Davis PJ, et al.  Inositol phosphates modulate binding of thyroid hormone to human red cell membranes in vitro. J Clin Endocrinol Metab. 1993;77:1427–1430
  13. Sundquist J, Blas SD, Hogan JE, et al.  The α1-adrenergic receptor in human erythrocyte membranes mediates interaction in vitro of epinephrine and thyroid hormone at the membrane Ca2+-ATPase. Cell Signal. 1992;4:795–799
  14. Davis PJ, Blas SD. In vitro stimulation of human red blood ell Ca2+-ATPase by thyroid hormone. Biochem Biophys Res Commun. 1981;99:1073–1080
  15. Davis FB, Davis PJ, Blas SD. Role of calmodulin in thyroid hormone stimulation in vitro of human erythrocyte Ca2+-ATPase activity. J Clin Invest. 1983;71:579–586
  16. Fiske CH, Subbarow Y. The colorimetric determination of phosphorus. J Biol Chem. 1925;66:375–400
  17. Lowry OH, Rosebrough NJ, Farr AL, et al.  Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193:265–275
  18. Ribeiro CMP, Dubay GR, Falck JR, et al.  Parathyroid hormone inhibits Na+-K+-ATPase through a cytochrome P-450 pathway. Am J Physiol. 1994;266:F497–F505
  19. Laemmli U. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970;227:680–685
  20. Majerus PW, Ross TS, Cunningham TW, et al.  Recent insights in phosphatidylinositol signaling. Cell. 1990;63:459–465
  21. Downes CP, Michell RH. The polyphosphoinositide phosphodiesterase of erythrocyte membrane. Biochem J. 1981;198:133–140
  22. Tremblay J, Cherkaoui L, Skuherska R, et al.  Increased inositol trisphosphate in erythrocytes of spontaneously hypertensive rats. J Hypertens. 1990;8:115–119
  23. Doughney C, McPherson MA, Goodchild MC, et al.  Increased phosphoinositide breakdown by phospholipase C in erythrocyte membranes from patients with cystic fibrosis. Clin Chim Acta. 1989;181:55–64
  24. Davis PJ, Davis FB, Lawrence WD. Thyroid hormone regulation of membrane Ca2+-ATPase activity. Endocr Res. 1989;15:651–682
  25. Davis FB, Cody V, Davis PJ, et al.  Stimulation by thyroid hormone analogues of red blood cell Ca2+-ATPase activity in vitro. J Biol Chem. 1983;258:12373–12377
  26. Mylotte KM, Cody V, Davis PJ, et al.  Milrinone and thyroid hormone stimulate myocardial membrane Ca2+-ATPase activity and share structural homologies. In: ed 12. Proc Natl Acad Sci USA. 82:1985;p. 7974–7978
  27. Warnick PR, Davis FB, Davis PJ, et al.  Differential activities of tolbutamide, tolazamide, and glyburide in vitro on rabbit myocardial membrane Ca2+-transporting ATPase activity. Diabetes. 1986;35:1044–1048
  28. Warnick PR, Davis FB, Mylotte KM, et al.  Calcium channel blocker inhibition of the calmodulin-dependent effects of thyroid hormone and milrinone on rabbit myocardial membrane Ca2+-ATPase activity. Biochem Pharmacol. 1988;37:2619–2623
  29. Deziel MR, Davis PJ, Davis FB, et al.  Interaction of amiodarone and its analogs with calmodulin. Arch Biochem Biophys. 1989;274:463–470
  30. Freissmuth M, Casey PJ, Gilman AG. G proteins control diverse pathways of transmembrane signaling. FASEB J. 1989;3:2125–2131
  31. Harden TK, Stephens L, Hawkins PT, et al.  Turkey erythrocyte membranes as a model for regulation of phospholipase C by guanine nucleotides. J Biol Chem. 1987;262:9057–9061
  32. Vaziri C, Downes CP. Association of a receptor and G-protein-regulated phospholipase C with the cytoskeleton. J Biol Chem. 1992;267:22973–22981
  33. English D, Akard LP, Taylor GS, et al.  Gp-regulated phosphoinositide hydrolysis in turkey and human erythrocytes exposed to fluoride ion: Relationship to calcium influx. J Lab Clin Med. 1992;119:87–98
  34. Iyengar R, Rich KA, Herberg JT, et al.  Identification of a new GTP-binding protein. J Biol Chem. 1987;262:9239–9245
  35. Carty DJ, Padrell E, Codina J, et al.  Distinct guanine nucleotide binding and release properties of the three Gi proteins. J Biol Chem. 1990;265:6268–6273
  36. DeFlora A, Damonte G, Sdraffa A, et al.  Heterogeneity of guanine nucleotide binding proteins in human red blood cell membranes. Adv Exp Med Biol. 1991;307:161–171
  37. Levine MA, Jap TS, Mauseth RS, et al.  Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: Biochemical, endocrine and genetic analysis of Albright's hereditary osteodystrophy in six kindreds. J Clin Endocrinol Metab. 1986;62:497–502
  38. Ribeiro-Neto F, Mattera R, Grenet D, et al.  Adenosine diphosphate ribosylation of G proteins by pertussis and cholera toxin in isolated membranes. In: Different requirements for and effects of guanine nucleotides and Mg2+. ed 12. Mol Endocrinol. 1:1987;p. 472–481

 Supported in part by Department of Veterans Affairs Merit Review funding (P.J.D.).

PII: 0026-0495(95)90238-4

Metabolism - Clinical and Experimental
Volume 44, Issue 7 , Pages 865-868 , July 1995