Prostaglandin F2α Stimulates Tyrosine Phosphorylation and Mitogen-Activated Protein Kinase in Osteoblastic MC3T3-E1 Cells via Protein Kinase C Activation.

Prostaglandin F2α Stimulates Tyrosine Phosphorylation and Mitogen-Activated Protein Kinase in Osteoblastic MC3T3-E1 Cells via Protein Kinase C Activation.
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前列腺素 F2α 通过蛋白激酶 C 激活刺激成骨细胞 MC3T3-E1 细胞中的酪氨酸磷酸化和丝裂原激活蛋白激酶。

DOI:
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发表时间:
1997
期刊:
影响因子:
4.8
通讯作者:
M. Kumegawa
M. Kumegawa
中科院分区:
医学2区
文献类型:
--
作者:
Y. Hakeda;M. Shiokawa;H. Mano;T. Kameda;L. Raisz;M. Kumegawa

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PGF2alpha stimulates the proliferation of clonal osteoblastic MC3T3-E1 cells via PGF2alpha receptor linked to phospholipase C activation. To elucidate intracellular events elicited by this receptor, we examined the effects of PGF2alpha on tyrosine phosphorylation and mitogen-activated protein kinase (MAPK) activity in MC3T3-E1 cells. PGF2alpha rapidly raised the level of phosphotyrosine of cellular proteins with Mr values of 62, 68, 72, 76, 82, 125, and 150 kDa. This PGF2alpha-induced tyrosine phosphorylation of proteins (except for pp62) was blocked by down-regulating protein kinase C (PKC) by 12-O-tetradecanoylphorbol 13-acetate pretreatment and by GF 109203X, a potent specific PKC inhibitor. The addition of PGF2alpha also transiently activated MAPK in the same range of concentrations that stimulated tyrosine phosphorylation. In addition, PGF2alpha augmented the MAPK kinase kinase activity of Raf-1, whereas basal activity of MAPK/extracellular signal-regulated protein kinase kinase was less than that of Raf-1 and was little affected by PGF2alpha. Like the tyrosine phosphorylation, these activations of Raf-1 and MAPK activities were reduced by inhibition and down-regulation of PKC. Genistein, a potent inhibitor of tyrosine kinases, did not block the Raf-1 induced by PGF2alpha, indicating a tyrosine kinase-independent pathway for Raf-1 activation. However, the tyrosine kinase inhibitor partially inhibited the MAPK activity, suggesting an involvement of another Raf-1-independent kinase cascade for activation of MAPK by PGF2alpha. Fluprostenol, a specific agonist of PGF2alpha receptor, mimicked the actions of PGF2alpha consistent with a PGF2alpha receptor pathway. Thus, the action of PGF2alpha on osteoblastic MC3T3-E1 cells appears to involve a single receptor that uses diverse interacting signal transduction systems.
前列腺素刺激的 UMR-106 细胞中 cAMP 和钙信使系统的关系。
DOI: --
发表时间: 1988
期刊: The Journal of biological chemistry
影响因子: --
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Yamaguchi,DT;Hahn,TJ;Beeker,TG;Kleeman,CR;Muallem,S
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前列腺素 F2 α 诱导的 MC3T3-E1 成骨细胞有丝分裂:蛋白激酶 C 介导的酪氨酸磷酸化的作用。
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