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Multiphasic generation of diacylglycerol in thrombin-activated human platelets.

机译:凝血酶激活的人类血小板中多酰基甘油的二相生成。

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摘要

The diacylglycerol (DAG)/protein kinase C pathway plays an important role in platelet aggregation and granule secretion. In this study, we examined the detailed kinetics of DAG formation in response to platelet stimulation. Both alpha- and gamma-thrombin caused multiphasic generation of DAG mass, with DAG production reaching peaks at 0.3-0.6 min intervals. A sub-threshold concentration of gamma-thrombin (1.5 nM) produced oscillations of DAG, but peak DAG levels rapidly returned to baseline (unstimulated) values. Intermediate concentrations of gamma-thrombin (8-30 nM) resulted in prominent phases of DAG production whose troughs became significantly elevated compared with baseline levels. This delayed accumulation of DAG coincided in time with the onset of secretion and irreversible aggregation. In contrast, stimulation of platelets with collagen resulted in delayed single-phase DAG production. The kinetics of DAG production in stimulated platelets may control both the timing and the degree of DAG accumulation. This may ensure that protein kinase C is activated optimally at the onset of secondary aggregation and secretion. This is the first report of oscillating DAG production in a biological system.
机译:二酰基甘油(DAG)/蛋白激酶C途径在血小板聚集和颗粒分泌中起重要作用。在这项研究中,我们检查了响应血小板刺激的DAG形成的详细动力学。 α-凝血酶和γ-凝血酶均引起多相DAG物质的产生,DAG的产生以0.3-0.6分钟的间隔达到峰值。亚阈值浓度的γ-凝血酶(1.5 nM)产生了DAG振荡,但DAG峰值水平迅速返回到基线(未刺激)值。中等浓度的γ-凝血酶(8-30 nM)导致DAG产生的突出阶段,其谷底与基线水平相比明显升高。 DAG的这种延迟积累与分泌的发生和不可逆的聚集在时间上相吻合。相反,用胶原蛋白刺激血小板导致延迟的单相DAG产生。受激血小板中DAG产生的动力学可以控制DAG积累的时机和程度。这可以确保蛋白激酶C在次级聚集和分泌开始时被最佳激活。这是在生物系统中振荡DAG生产的第一份报告。

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