Pasquet J M, Dachary-Prigent J, Nurden A T
UMR 5533 CNRS, Hôpital Cardiologique, 33604 Pessac, France.
Biochem J. 1998 Aug 1;333 ( Pt 3)(Pt 3):591-9. doi: 10.1042/bj3330591.
Phosphatidylserine exposure and microvesicle release give rise to procoagulant activity during platelet activation. We have previously shown that whereas the Ca2+ ionophore A23187 and 2,5-di-(t-butyl)-1, 4-benzohydroquinone, a Ca2+-ATPase inhibitor, induce phosphatidylserine exposure, only the former triggers microvesicle release. We now report that microvesicle formation with ionophore A23187 is specifically associated with mu-calpain activation, increased protein tyrosine phosphatase (PTP) activity and decreased tyrosine phosphorylation. The degree to which calpain and individual PTPs were activated in response to A23187 depended on the extent of bivalent cation chelation in the external medium. EGTA (2 mM) blocked or severely retarded their activation, and addition of extracellular Ca2+ in excess (2 mM) resulted in virtually immediate tyrosine dephosphorylation. Dephosphorylation was correlated with an increase in total PTP activity in platelet lysates. In platelets stimulated by a combination of thrombin and collagen, only the subpopulation undergoing microvesicle release and isolated by their binding to annexin-V-coated magnetic beads exhibited protein tyrosine dephosphorylation. Detection of PTP activity in an 'in-gel' assay showed the Ca2+-dependent appearance of active low-molecular-mass bands at 38, 36 and 27 kDa. Individual PTPs varied in their protease sensitivity to changes in intracellular Ca2+ levels. For example, PTP1B was a more sensitive substrate than SH2-domain-containing tyrosine phosphatase-1 for mu-calpain cleavage. Incubation of platelets with the PTP inhibitors, phenylarsine oxide and benzylphosphonic acid acetoxymethyl ester, led to increased tyrosine phosphorylation and the surface expression of aminophospholipids but little microvesicle formation. Furthermore, microvesicle release in response to ionophore A23187 was inhibited. We conclude that platelet microvesicle formation is associated with extensive protein tyrosine dephosphorylation.
在血小板活化过程中,磷脂酰丝氨酸暴露和微泡释放会引发促凝血活性。我们之前已经表明,虽然钙离子载体A23187和Ca²⁺ -ATP酶抑制剂2,5 -二 -(叔丁基)-1,4 -苯二酚可诱导磷脂酰丝氨酸暴露,但只有前者能触发微泡释放。我们现在报告,用离子载体A23187形成微泡与μ - 钙蛋白酶激活、蛋白酪氨酸磷酸酶(PTP)活性增加以及酪氨酸磷酸化减少特别相关。响应A23187时,钙蛋白酶和单个PTP的激活程度取决于外部介质中二价阳离子螯合的程度。EGTA(2 mM)会阻断或严重延迟它们的激活,而过量添加细胞外Ca²⁺(2 mM)实际上会立即导致酪氨酸去磷酸化。去磷酸化与血小板裂解物中总PTP活性的增加相关。在由凝血酶和胶原蛋白联合刺激的血小板中,只有通过与膜联蛋白V包被的磁珠结合而分离出的经历微泡释放的亚群表现出蛋白酪氨酸去磷酸化。“凝胶内”分析中PTP活性的检测显示,在38、36和27 kDa处出现了Ca²⁺ 依赖性的活性低分子量条带。单个PTP对细胞内Ca²⁺ 水平变化的蛋白酶敏感性各不相同。例如,对于μ - 钙蛋白酶裂解,PTP1B比含SH2结构域的酪氨酸磷酸酶 - 1更敏感。用PTP抑制剂氧化苯胂和苄基膦酸乙酰氧基甲酯孵育血小板会导致酪氨酸磷酸化增加以及氨基磷脂的表面表达增加,但微泡形成很少。此外,对离子载体A23187的微泡释放受到抑制。我们得出结论,血小板微泡形成与广泛的蛋白酪氨酸去磷酸化相关。