Thromb Haemost 2004; 92(01): 104-113
DOI: 10.1160/TH03-10-0631
Platelets and Blood Cells
Schattauer GmbH

Apoptotic-like mitochondrial events associated to phosphatidylserine exposure in blood platelets induced by local anaesthetics

Olivier Augereau
1   Physiologie Mitochondriale, Université Victor Segalen-Bordeaux 2, Bordeaux Cedex, France
,
Rodrigue Rossignol
1   Physiologie Mitochondriale, Université Victor Segalen-Bordeaux 2, Bordeaux Cedex, France
,
Francesca DeGiorgi
2   Signalisation et mécanisme moléculaire de l’apoptose, E347 INSERM, Institut Européen de Chimie-Biologie, Pessac, France
,
Jean-Pierre Mazat
1   Physiologie Mitochondriale, Université Victor Segalen-Bordeaux 2, Bordeaux Cedex, France
,
Thierry Letellier
1   Physiologie Mitochondriale, Université Victor Segalen-Bordeaux 2, Bordeaux Cedex, France
,
Jeanne Dachary-Prigent
1   Physiologie Mitochondriale, Université Victor Segalen-Bordeaux 2, Bordeaux Cedex, France
› Author Affiliations
Financial support: This work was supported by the Agence Française du Sang, the Groupe d’Etude sur l’Hémostase et la Thrombose, the Institut National pour la Santé et la Recherche Médicale, the Université de Bordeaux 2 and the Conseil Régional d’Aquitaine.
Further Information

Publication History

Received 16 October 2003

Accepted after revision 29 March 2004

Publication Date:
29 November 2017 (online)

Summary

Phosphatidylserine exposure in platelets is required for normal haemostasis and is also a hallmark of apoptosis. It results from activation of a phospholipid scramblase, which has been shown to be differently stimulated by Ca2+-influx and during apoptosis, thus suggesting that mitochondria may be involved in phosphatidylserine exposure in platelets. It is also well known that local anaesthetics can expose phosphatidylserine in platelets and affect the mitochondrial metabolism in other cells. Thus, the present study was undertaken to evaluate the specific involvement of mitochondria in phosphatidylserine exposure in platelets. For this purpose, we stimulated phosphatidylserine exposure by local anaesthetics and avoided any external Ca2+-influx by performing all experiments in the absence of added Ca2+. We report that phosphatidylserine exposure, induced by the lipophilic local anaesthetics dibucaine and tetracaine, was accompanied by depolarization of the mitochondrial membrane, cytochrome c release, calpain-processing of caspases 9 and 3 to active enzymes, as well as a prolonged increase in both cytosolic and mitochondrial Ca2+ concentrations. In contrast, in the absence of extracellular Ca2+, the Ca2+-ionophore A23187 induced a smaller transient increase in both cytosolic and mitochondrial Ca2+ concentrations, but did not induce any other phenomena, nor phosphatidylserine exposure. However, phosphatidylserine exposure and depolarization induced by dibucaine still occurred in spite of inhibition of intracellular Ca2+ elevation. Thus we conclude that phosphatidylserine exposure in platelets is associated with mitochondrial apoptotic-like events. Therefore, we propose that mitochondria engagement in an apoptotic pathway in platelets could lead to PS exposure without the participation of Ca2+.

 
  • References

  • 1 Zwaal RF. Membrane involvement in blood coagulation. Biochim Biophys Acta 1978; 515: 163-205.
  • 2 Williamson P, Kulick A, Zachowski A. et al. Ca2+ induces transbilayer redistribution of all major phospholipids in human erythrocytes. Biochemistry 1992; 14: 6355-60.
  • 3 Zwaal RF, Comfurius P, Bevers EM. Mechanism and function of changes in membrane-phospholipid asymmetry in platelets and erythrocytes. Biochem Soc Trans 1993; 21: 248-53.
  • 4 Basse F, Stout JG, Sims PJ. et al. Isolation of an erythrocyte membrane protein that mediates Ca2+-dependent transbilayer movement of phospholipid. J Biol Chem 1996; 271: 17205-10.
  • 5 Fadok VA, Bratton DL, Frasch SC. et al. The role of phosphatidylserine in recognition of apoptotic cells by phagocytes. Cell Death Differ 1998; 05: 549-50.
  • 6 Bertino AM, Qi XQ, Li J. et al. Apoptotic markers are increased in platelets stored at 37 degrees C. Transfusion 2003; 43: 857-66.
  • 7 Leytin V, Freedman J. Platelet apoptosis in stored platelet concentrates and other models. Transfus Apheresis Sci 2003; 28: 285-95.
  • 8 Wolf BB, Goldstein JC, Stennicke HR. et al. Calpain functions in a caspase-independent manner to promote apoptosis-like events during platelet activation. Blood 1999; 94: 1683-92.
  • 9 Scherbina A, Remold-O’-Donnell E. Role of caspase in a subset of human platelet activation responses. Blood 1999; 93: 4222-31.
  • 10 Bratton DL, Fadok VA, Richter DA. et al. Appearance of phosphatidylserine on apoptotic cells requires calcium-mediated nonspecific flip-flop and is enhanced by loss of the aminophospholipid translocase. J Biol Chem 1997; 272: 26159-65.
  • 11 Williamson P, Christie A, Kohlin T. et al. Phospholipid scramblase activation pathways in lymphocytes. Biochemistry 2001; 40: 8065-72.
  • 12 Verhallen PF, Bevers EM, Comfurius P. et al. Correlation between calpain-mediated cytoskeletal degradation and expression of platelet procoagulant activity. A role for the platelet membrane-skeleton in the regulation of membrane lipid asymmetry?. Biochem Biophys Acta 1987; 903: 206-17.
  • 13 Dachary-Prigent J, Freyssinet J-M, Pasquet J-M. et al. Annexin V as a probe of aminophospholipid exposure and platelet membrane vesiculation: a flow cytometry study showing a role for free sulfhydryl groups. Blood 1993; 08: 2554-65.
  • 14 Arita K, Utsumi T, Kato A. et al. Mechanism of dibucaine-induced apoptosis in promyelocytic leukemia cells (HL-60). Biochem Pharm 2000; 60: 905-15.
  • 15 He J, Xiao Y, Casiano CA. et al. Role of mitochondrial cytochrome c in cocaine-induced apoptosis in coronary artery endothelial cells. J Pharmacol Exp Therapy 2000; 295: 896-903.
  • 16 Sztark F, Tueux O, Erny P. et al. Effects of bupivacaine on cellular oxygen consumption and adenine nucleotide metabolism. Anesth Analg 1994; 78: 335-39.
  • 17 Grouselle M, Tueux O, Dabadie P. et al. Effect of local anaesthetics on mitochondrial membrane potential in living cells. Biochem J 1990; 271: 269-72.
  • 18 Sztark F, Malgat M, Dabadie P. et al. Comparison of the effects of bupivacaine and ropivacaine on heart cell mitochondrial bioenergetics. Anesthesiology 1998; 88: 1340-9.
  • 19 Pulselli R, Arcuri E, Paggi MG. et al. Changes in membrane potential induced by local anesthetic bupivacaine on mitochondria within Ehrlich ascites tumor cells. Oncol Res 1996; 08: 267-71.
  • 20 Garcia-Martin E, Escudero B, Fernandez-Salguero P. et al. Modulation of (Ca2+ +Mg2+)-ATPases and Ca2+ fluxes through the plasma membrane of synaptosomes and sarcoplasmic reticulum by local anaesthetics. Biochem Soc Trans 1989; 17: 960-2.
  • 21 Barghouthi SA, Puri RK, Eftink MR. Local anesthetic-phospholipid interactions. Effects of ionic strength, temperature, and phospholipid mixtures on the binding of dibucaine to phospholipids. Biophys Chem 1993; 46: 1-11.
  • 22 Papahadjopoulos D, Jacobson K, Poste G. et al. Effect of local anesthetics on membrane properties. Change in the fluidity of phospholipid bilayers. Biochim Biophys Acta 1975; 394: 504-19.
  • 23 Ronot X, Benel L, Adolphe M. et al. Mitochondrial analysis in living cells: the use of rhodamine 123 and flow cytometry. Biol Cell 1986; 57: 1-7.
  • 24 McIntyre JC, Sleight RG. Fluorescence assay for phospholipid membrane asymmetry. Biochemistry 1991; 30: 11819-27.
  • 25 Dachary-Prigent J, Pasquet JM, Freyssinet JM. et al. Calcium involvement in aminophospholipid exposure and microparticle formation during platelet activation: a study using Ca2+ ATPase inhibitors. Biochemistry 1995; 36: 11625-34.
  • 26 Chazotte B, Vanderkooi G. Multiple sites of inhibition of mitochondrial electron transport by local anaestheticss. Biochim Biophys Acta 1981; 636: 153-61.
  • 27 Chua BT, Guo K, Li P. Direct cleavage by the calcium-activated protease calpain can lead to inactivation of caspases. J Biol Chem 2000; 275: 5131-5.
  • 28 Ichas F, Mazat JP. From calcium signaling to cell death: two conformations for the mitochondrial permeability transition pore. Switching from low-to high-conductance state. Biochim Biophys Acta 1998; 1366: 33-50.
  • 29 Low PS, Lloyd DH, Stein TM. et al. Calcium displacement by local anaestheticss. J Biol Chem 1979; 254: 4119-25.
  • 30 Takara D, Sanchez GA, Alonso GL. Effect of carticaine on the sarcoplasmic reticulum triphosphatase. Naunyn Schmiedebergs Arch Pharmacol 2000; 362: 497-503.
  • 31 Zink W, Graf BM, Sinner B. et al. Differential effect of bupivacaine on intracellular Ca2+ regulation: potential mechanisms of its myotoxicity. Anesthesiology 2002; 97: 710-6.
  • 32 Dawson AP, Fulton DV. The action of nupervacaine on calcium efflux from rat liver mitochondria. Biochem J 1980; 188: 749-55.
  • 33 Jurkowitz MS, Geisbuhler T, Jung DW. et al. Ruthenium red-sensitive and -insensitive release of Ca2+ from uncoupled heart mitochondria. Arch Biochem Biophys 1983; 223: 120-8.
  • 34 Stout JG, Basse F, Luhm RA. et al. Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids. J Clin Invest 1997; 99: 2232-8.
  • 35 Meisenholder GW, Martin SJ, Green DR. et al. Events in apoptosis. Acidification is downstream of protease activation and BCL-2 protection. J Biol Chem 1996; 271: 16260-2.
  • 36 Rodeau JL, Flament S, Browaeys E. et al. Effect of procaine on membrane potential and intracellular pH in Xenopus laevis oocytes. Mol Membr Biol 1998; 15: 145-51.
  • 37 Frasch SC, Henson PM, Kailey JM. et al. Regulation of phospholipid scramblase activity during apoptosis and cell activation by protein kinase C delta. J Biol Chem 2000; 275: 23065-73.
  • 38 Kagan VE, Fabisiak JP, Shvedova AA. et al. Oxidative signaling pathway for externalization of plasma membrane phosphatidylserine during apoptosis. FEBS Lett 2000; 477: 1-7.
  • 39 Dachary-Prigent J, Pasquet JM, Freyssinaud E. et al. Aminophospholipid exposure, microvesiculation in the platelets of a patient with Scott syndrome : a study using phisiologic agonists and local anesthetics. Brit J Haematol 1997; 99: 959-67.
  • 40 Breslin DS, Martin G, Macleod DB. et al. Central nervous system toxicity following the administration of levobupivacaine for lumbar plexus block: A report of two cases. Reg Anesth Pain Med 2003; 28: 144-7.
  • 41 Zurbano MJ, Heras M, Rigol M. et al. Cocaine administration enhances platelet reactivity to subendothelial components: studies in a pig model. Eur J Clin Invest 1997; 27: 116-20.
  • 42 Closse C, Dachary-Prigent J, Boisseau MR. Phosphatidylserine-related adhesion of humain erythocytes to vascular endothelium. Brit J Haematol 1999; 107: 300-2.
  • 43 Hultin MB, Hennessey J, Morrison SA. Dibucaine elicits platelet procoagulant activity in factor VIII and factor X activation by a mechanism involving a sulphydryl-dependent enzyme. Thromb Res 1992; 68: 399-407.
  • 44 Heesch CM, Wilhem CR, Ristich J. et al. Cocaine activates platelets and inceases the formation of circulating platelets containing microaggregates in humains. Heart 2000; 83: 388-95.