Thromb Haemost 1989; 61(01): 010-014
DOI: 10.1055/s-0038-1646518
Original Article
Schattauer GmbH Stuttgart

Impaired Energy Metabolism in Platelets from Patients with Wiskott-Aldrich Syndrome

Adrie J M Verhoeven
The Department of Haematology, University Hospital Utrecht, The Netherlands
,
Irene E A van Oostrum
The Department of Haematology, University Hospital Utrecht, The Netherlands
,
Hans van Haarlem
The Department of Haematology, University Hospital Utrecht, The Netherlands
,
Jan-Willem N Akkerman
The Department of Haematology, University Hospital Utrecht, The Netherlands
› Author Affiliations
Further Information

Publication History

Received 13 July 1988

Accepted after revision 10 October 1988

Publication Date:
24 July 2018 (online)

Summary

The platelet function defect seen in patients with Wiskott- Aldrich syndrome (WAS) has been ascribed to abnormal mitochondrial energy generation. The present study reveals a reduced energy content and low adenylate energy charge in platelets from two WAS-patients. Energy consumption in the resting platelets is slightly beyond the normal range, especially when ATP-resynthesis is primarily glycolytic. When platelets are stimulated with thrombin, the increase in energy consumption is 40-60% lower than in controls, both when energy is produced in glycolysis as when the mitochondria supply most of the energy. Analysis of the electron transport chain reveals no abnormalities. In contrast, the balance between glycolytic and mitochondrial ATP resynthesis is disturbed with a lowered contribution of oxidative ATP production. No such abnormalities are found in two WAS-carriers with the exception of a slight impairment in energy consumption during stimulation with thrombin. Thus, the platelet malfunction in WAS may be caused by a defect in the regulation of energy generation.

 
  • References

  • 1 Baldini MG. Nature of the platelet defect in the Wiskott-Aldrich syndrome. Ann N Y Acad Sci 1972; 201: 437-444
  • 2 Grottum KA, Hovig T, Holmsen H, Foss Abrahamsen A, Jeremia M, Seip M. Wiskott-Aldrich Syndrome: Qualitative platelet defects and short platelet survival. Br J Haematol 1969; 17: 373-388
  • 3 Kuramoto H, Steiner M, Baldini MG. Lack of platelet response to stimulation of the Wiskott-Aldrich syndrome. N Engl J Med 1970; 282: 475-479
  • 4 Marone G, Albini F, Di Martino L, Quattrin S, Poto S, Condorelli M. The Wiskott-Aldrich syndrome: studies of platelets, basophils and polymorphonuclear leucocytes. Br J Haematol 1986; 62: 737-745
  • 5 Shapiro RS, Gerrard JM, Perry GS, White JG, Krivit W, Kersey JH. Wiskott-Aldrich syndrome: detection of carrier state by metabolic stress of platelets. Lancet I 1978; 121: 123
  • 6 Gerrard JM, Blease RM, Perry GS, Krivit W, Shapiro RS, Kersey JH, Spector B, White JG. Further studies of a metabolic stress test in Wiskott-Aldrich syndrome carriers. Am J Pediatric Hematol 1980; 2: 25-30
  • 7 Akkerman JW, van Brederode W, Gorter G, Zegers BJ, Kuis W. Wiskott-Aldrich syndrome: studies on a possible defect in mitochondrial ATP resynthesis in platelets. Br J Haematol 1982; 51: 561-568
  • 8 Rijksen G, Akkerman JW, van den Wall BakeA W L, Pott Hofstede D, Staal GE J. Generalized hexokinase deficiency in the blood cells of a patient with nonspherocytic hemolytic anemia. Blood 1983; 61: 12-18
  • 9 Akkerman JW, Rijksen G, Gorter G, Staal GE J. Platelet functions and energy metabolism in a patient with hexokinase deficiency. Blood 1984; 63: 147-153
  • 10 Walsh PN. Albumin density gradient separation and washing of platelets and the study of platelet coagulant activities. Br J Haematol 1972; 22: 205-217
  • 11 Aharony D, Smith JB, Silver MJ. Regulation of arachidonate- induced platelet aggregation by the lipoxygenase product, 12-hydroperoxy eicosatetraenoic acid. Biochim Biophys Acta 1982; 718: 193-200
  • 12 Daniel JL, Molish IR, Holmsen H. Radioactive labeling of the adenine nucleotide pool of cells as a method to distinguish amongintracellular compartments. Studies on human platelets Biochim Biophys Acta 1980; 632: 444-553
  • 13 Holmsen H, Day HJ, Setkowsky CA. Behaviour of adenine nucleotides during the platelet release reaction induced by ADP and adrenaline. Biochem J 1972; 129: 67-82
  • 14 Atkinson DE. Cellular Energy Metabolism and Its Regulation. Academic Press; New York: 1977. pp 40-50
  • 15 Akkerman JW, Gorter G, Schrama L, Holmsen HA. Novel technique for rapid determination of energy consumption in platelets. Demonstration of different energy consumption associated with three secretory responses Biochemistry 1983; 210: 145-155
  • 16 Verhoeven AJ M, Mommersteeg ME, Akkerman JW N. Quantification of energy consumption in platelets during thrombin-induced aggregation and secretion. Tight coupling between platelet responses and the increment in energy consumption Biochem J 1984; 221: 777-787
  • 17 Verhoeven AJ M, Gorter G, Mommersteeg ME, Akkerman JW N. The energetics of early platelet responses. Energy consumption during shape change and aggregation with special reference to protein phosphorylation and the polyphosphoinositide cycle Biochem J 1985; 228: 451-462
  • 18 Verhoeven AJ M, Mommersteeg ME, Akkerman JW N. Balanced contribution of glycolytic and adenylate pool in supply of metabolic energy in platelets. J Biol Chem 1985; 260: 2621-2624
  • 19 Verhoeven AJ M, Mommersteeg ME, Akkerman JW N. Comparative studies on the energetics of platelet responses induced by different agonists. Biochem J 1986; 236: 879-887
  • 20 Karpatkin S. Studies on human platelet glycolysis Effect of glucose, cyanide, insulin, citrate, and agglutination and contraction on platelet glycolysis. J Clin Invest 1967; 46: 409-417
  • 21 Akkerman JW, Ebberink RH M, Lips JP M, Christiaens GC M L. Rapid separation of cytosol and particle fraction of human platelets by digitonin-induced cell damage. Br J Haematol 1980; 44: 291-300
  • 22 Pickett WC, Cohen P. Influence of medium tonicity on respiration by suspensions of human platelets. Am J Physiol 1976; 231: 185-190
  • 23 Holmsen H, Robkin L. Hydrogen peroxide lowers ATP levels in platelets without altering adenylate energy charge and platelet function. J Biol Chem 1977; 252: 1752-1757
  • 24 Akkerman JW N, Gorter G, Holmsen H. Reversibility of the inhibition of platelet responses by ATP-deprivationClose correlation between responses and adenylate energy charge during transient substrate depletion. Biochim Biophys Acta 1983; 760: 34-41
  • 25 Bustamante E, Morris HP, Pedersen PL. Energy metabolism of tumor cells. Requirement for a form of hexokinase with a propensity for mitochondrial binding J Biol Chem 1981; 256: 8699-8704
  • 26 Wilson JE. Brain hexokinase, the prototype ambiquitous enzyme. In Current Topics in Cellular Regulation. Horecker BL, Stadtmann ER. (eds) Academic Press; New York: 1980. Vol 16 pp 1-54
  • 27 Fiek C, Benz R, Roos N, Brdiczka D. Evidence for identitiy between hexokinase-binding protein and the mitochondrial porin in the outer membrane of rat liver mitochondria. Biochim Biophys Acta 1982; 668: 429-440
  • 28 Rijksen G, Staal GE, Beks PJ, Streefkerk M, Akkerman J WN. Compartmentation of hexokinase in human blood cells.Characterization of soluble and particulate enzymes. Biochim Biophys Acta 1982; 719: 431-437