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P2嘌呤受体刺激内皮前列环素生成需要p42和p44丝裂原活化蛋白激酶的磷酸化和激活。

Phosphorylation and activation of p42 and p44 mitogen-activated protein kinase are required for the P2 purinoceptor stimulation of endothelial prostacyclin production.

作者信息

Patel V, Brown C, Goodwin A, Wilkie N, Boarder M R

机构信息

Department of Cell Physiology and Pharmacology, University of Leicester, U.K.

出版信息

Biochem J. 1996 Nov 15;320 ( Pt 1)(Pt 1):221-6. doi: 10.1042/bj3200221.

Abstract

Extracellular ATP and ADP, released from platelets and other sites stimulate the endothelial production of prostacyclin (PGI2) by acting on G-protein-coupled P2Y2 and P2Y2 purinoceptors, contributing to the maintenance of a non-thrombogenic surface. The mechanism, widely described as being dependent on elevated cytosolic [Ca2+], also requires protein tyrosine phosphorylation. Here we show that activation of both these P2 receptor types leads to the tyrosine phosphorylation and activation of both the p42 and p44 forms of mitogen-activated protein kinase (MAPK). 2-Methylthio-ATP and UTP, selectively activating P2Y1 and P2Y2 purinoceptors respectively, and ATP, a non-selective agonist at these two receptors, stimulate the tyrosine phosphorylation of both p42mapk and p44mapk, as revealed by Western blots with an antiserum specific for the tyrosine-phosphorylated forms of the enzymes. By using separation on Resource Q columns, peptide kinase activity associated with the phosphorylated MAPK enzymes distributes into two peaks, one mainly p42mapk and one mainly p44mapk, both of which are stimulated by ATP with respect to kinase activity and phospho-MAPK immunoreactivity. Stimulation of P2Y1 or P2Y2 purinoceptors leads to a severalfold increase in PGI2 efflux; this was blocked in a dose-dependent manner by the selective MAPK kinase inhibitor PD98059. This drug also blocked the agonist-stimulated increase in phospho-MAPK immunoreactivity for both p42mapk and p44mapk but left the phospholipase C response to P2 agonists essentially unchanged. Olomoucine has been reported to inhibit p44mapk activity. Here we show that in the same concentration range olomoucine inhibits activity in both peaks from the Resource Q column and also the agonist stimulation of 6-keto-PGF1, but has no effect on agonist-stimulated phospho-MAPK immunoreactivity. These results provide direct evidence for the involvement of p42 and p44 MAPK in the PGI2 response of intact endothelial cells: we have shown that both the endothelial P2Y purinoceptors are linked to activation of MAPK, and that activation of this pathway is a requirement for the stimulation by ATP/ADP of endothelial PGI2 production.

摘要

从血小板和其他部位释放的细胞外ATP和ADP,通过作用于G蛋白偶联的P2Y2嘌呤受体,刺激内皮细胞生成前列环素(PGI2),有助于维持非血栓形成表面。这种机制,广泛描述为依赖于胞质[Ca2+]升高,也需要蛋白质酪氨酸磷酸化。在这里,我们表明这两种P2受体类型的激活导致有丝分裂原激活蛋白激酶(MAPK)的p42和p44形式的酪氨酸磷酸化和激活。分别选择性激活P2Y1和P2Y2嘌呤受体的2-甲硫基-ATP和UTP,以及这两种受体的非选择性激动剂ATP,刺激p42mapk和p44mapk的酪氨酸磷酸化,这通过用针对该酶酪氨酸磷酸化形式的抗血清进行的蛋白质印迹法得以揭示。通过在Resource Q柱上进行分离,与磷酸化MAPK酶相关的肽激酶活性分布为两个峰,一个主要是p42mapk,一个主要是p44mapk,就激酶活性和磷酸化MAPK免疫反应性而言,两者都受到ATP的刺激。刺激P2Y1或P2Y2嘌呤受体导致PGI2流出增加数倍;这被选择性MAPK激酶抑制剂PD98059以剂量依赖性方式阻断。该药物还阻断了激动剂刺激的p42mapk和p44mapk的磷酸化MAPK免疫反应性增加,但使磷脂酶C对P2激动剂的反应基本不变。据报道,olomoucine可抑制p44mapk活性。在这里,我们表明在相同浓度范围内,olomoucine抑制Resource Q柱上两个峰的活性以及激动剂对6-酮-PGF1的刺激,但对激动剂刺激的磷酸化MAPK免疫反应性没有影响。这些结果为p42和p44 MAPK参与完整内皮细胞的PGI2反应提供了直接证据:我们已经表明内皮P2Y嘌呤受体都与MAPK的激活有关,并且该途径的激活是ATP/ADP刺激内皮PGI2产生的必要条件。

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