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在 Ca2+存在的情况下,蛋白激酶 C 的亚最大抑制恢复了 ADP 诱导的血小板致密颗粒分泌。

Submaximal inhibition of protein kinase C restores ADP-induced dense granule secretion in platelets in the presence of Ca2+.

机构信息

Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.

出版信息

J Biol Chem. 2011 Jun 17;286(24):21073-82. doi: 10.1074/jbc.M110.187138. Epub 2011 Apr 13.

Abstract

Protein kinase C (PKC) is a family of serine/threonine kinases that play isoform-specific inhibitory and stimulatory roles in platelet activation. We show here that the pan-PKC inhibitor Ro31-8220 can be used to dissect these events following platelet activation by ADP. Submaximal concentrations of Ro31-8220 potentiated aggregation and dense granule secretion to ADP in plasma anticoagulated with citrate, in D-Phe-Pro-Arg-chloromethyl ketone-anticoagulated plasma, which has physiological levels of Ca(2+), and in washed platelets. Potentiation was retained on inhibition of cyclooxygenase and was associated with an increase in intracellular Ca(2+). Potentiation of aggregation and secretion was abolished by a maximally effective concentration of Ro31-8220, consistent with a critical role of PKC in secretion. ADP-induced secretion was potentiated in the presence of an inhibitor of PKCβ but not in the presence of available inhibitors of other PKC isoforms in human and mouse platelets. ADP-induced secretion was also potentiated in mouse platelets deficient in PKCε but not PKC. These results demonstrate that partial blockade of PKC potentiates aggregation and dense granule secretion by ADP in association with increased Ca(2+). This provides a molecular explanation for the inability of ADP to induce secretion in plasma in the presence of physiological Ca(2+) concentrations, and it reveals a novel role for PKC in inhibiting platelet activation by ADP in vivo. These results also demonstrate isoform-specific inhibitory effects of PKC in platelets.

摘要

蛋白激酶 C(PKC)是丝氨酸/苏氨酸激酶家族,在血小板激活中发挥同工型特异性抑制和刺激作用。我们在此表明,泛 PKC 抑制剂 Ro31-8220 可用于在 ADP 激活血小板后解析这些事件。在柠檬酸抗凝的血浆中、在具有生理 Ca2+浓度的 D-Phe-Pro-Arg-氯甲基酮抗凝的血浆中和在洗涤过的血小板中,亚最大浓度的 Ro31-8220 增强了对 ADP 的聚集和致密颗粒分泌。在抑制环氧化酶的情况下,增强作用得以保留,并且与细胞内 Ca2+的增加有关。最大有效浓度的 Ro31-8220 可消除聚集和分泌的增强作用,这与 PKC 在分泌中的关键作用一致。在人血小板和鼠血小板中,PKCβ抑制剂存在时,ADP 诱导的分泌增强,但其他 PKC 同工型的可用抑制剂存在时,ADP 诱导的分泌增强。在缺乏 PKCε但不缺乏 PKC 的鼠血小板中,ADP 诱导的分泌也增强。这些结果表明,PKC 的部分阻断与 Ca2+增加一起增强了 ADP 诱导的聚集和致密颗粒分泌。这为在生理 Ca2+浓度存在下 ADP 不能诱导血浆中分泌提供了分子解释,并且揭示了 PKC 在体内抑制 ADP 诱导的血小板激活中的新作用。这些结果还证明了 PKC 在血小板中的同工型特异性抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e31/3122168/926e943a96a6/zbc0281165820001.jpg

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