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PC12细胞中丝裂原活化蛋白激酶(MAP激酶)级联反应的调控:B-Raf激活MEK-1(丝裂原活化蛋白激酶或细胞外信号调节激酶)并受环磷酸腺苷(cAMP)抑制。

Regulation of the MAP kinase cascade in PC12 cells: B-Raf activates MEK-1 (MAP kinase or ERK kinase) and is inhibited by cAMP.

作者信息

Peraldi P, Frödin M, Barnier J V, Calleja V, Scimeca J C, Filloux C, Calothy G, Van Obberghen E

机构信息

INSERM U 145, Faculté de Médecine, Nice, France.

出版信息

FEBS Lett. 1995 Jan 9;357(3):290-6. doi: 10.1016/0014-5793(94)01376-c.

Abstract

In PC12 cells, cAMP stimulates the MAP kinase pathway by an unknown mechanism. Firstly, we examined the role of calcium ion mobilization and of protein kinase C in cAMP-stimulated MAP kinase activation. We show that cAMP stimulates p44mapk independently of these events. Secondly, we studied the role of B-Raf in this process. We observed that NGF, PMA and cAMP induce the phosphorylation of B-Raf as well as an upward shift in its electrophoretic mobility. We show that B-Raf is activated following NGF and PMA treatment of PC12 cells, and that it can phosphorylate and activate MEK-1. However, cAMP inhibits B-Raf autokinase activity as well as its ability to phosphorylate and activate MEK-1. This inhibition is likely to be due to a direct effect since we found that PKA phosphorylates B-Raf in vitro. Further, we show that B-Raf binds to p21ras, but more important, this binding to p21ras is virtually abolished with B-Raf from PC12 cells treated with CPT-cAMP. Hence, these data indicate that the PKA-mediated phosphorylation of B-Raf hampers its interaction with p21ras, which is responsible for the PKA-mediated decrease in B-Raf activity. Finally, our work suggests that in PC12 cells, cAMP stimulates MAP kinase through the activation of an unidentified MEK kinase and/or the inhibition of a MEK phosphatase.

摘要

在PC12细胞中,环磷酸腺苷(cAMP)通过一种未知机制刺激丝裂原活化蛋白激酶(MAP激酶)信号通路。首先,我们研究了钙离子动员和蛋白激酶C在cAMP刺激的MAP激酶激活过程中的作用。我们发现,cAMP刺激p44mapk的过程与这些事件无关。其次,我们研究了B-Raf在这一过程中的作用。我们观察到,神经生长因子(NGF)、佛波酯(PMA)和cAMP均可诱导B-Raf的磷酸化及其电泳迁移率的上移。我们发现,在PC12细胞经NGF和PMA处理后,B-Raf被激活,并且它能够磷酸化并激活MEK-1。然而,cAMP抑制B-Raf自身激酶活性及其磷酸化和激活MEK-1的能力。这种抑制作用可能是直接作用的结果,因为我们发现蛋白激酶A(PKA)在体外可磷酸化B-Raf。此外,我们发现B-Raf与p21ras结合,但更重要的是,用环磷腺苷(CPT-cAMP)处理PC12细胞后,B-Raf与p21ras的这种结合几乎完全消失。因此,这些数据表明,PKA介导的B-Raf磷酸化阻碍了其与p21ras的相互作用,这正是PKA介导的B-Raf活性降低的原因。最后,我们的研究表明,在PC12细胞中,cAMP通过激活一种未明确的MEK激酶和/或抑制一种MEK磷酸酶来刺激MAP激酶。

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