The cyclic adenosine monophosphate-dependent protein kinase (PKA) is required for the sustained activation of mitogen-activated kinases and gene expression by nerve growth factor

被引:122
作者
Yao, H
York, RD
Misra-Press, A
Carr, DW
Stork, PJS
机构
[1] Oregon Hlth Sci Univ, Vollum Inst Adv Biomed Res, Portland, OR 97201 USA
[2] Oregon Hlth Sci Univ, Dept Mol Microbiol & Immunol, Portland, OR 97201 USA
[3] Oregon Hlth Sci Univ, Grad Program Neurosci, Portland, OR 97201 USA
[4] Oregon Hlth Sci Univ, Dept Pathol, Portland, OR 97201 USA
[5] Oregon Hlth Sci Univ, Dept Cell & Dev Biol, Portland, OR 97201 USA
[6] Oregon Hlth Sci Univ, Vet Affairs Med Ctr, Portland, OR 97201 USA
[7] Oregon Hlth Sci Univ, Div Endocrinol, Portland, OR 97201 USA
关键词
D O I
10.1074/jbc.273.14.8240
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Induction of neuronal differentiation of the rat pheochromocytoma cell line, PC12 cells, by nerve growth factor (NGF) requires activation of the mitogen-activated protein (MAP) kinase or extracellular signal-regulated kinase (ERK). cAMP-dependent protein kinase (protein kinase A (PKA)) also call induce differentiation of these cells. Like NGF, the ability of PKA. to differentiate PC12 cells is associated with a sustained activation of ERKs, Here we show that maximal sustained activation of ERK1 by NGF requires PKA, Inhibitors of PKA partially blocked activation of ERK1 by NGF but had no effect on activation of ERK1 by EGF. Inhibition of PRA also reduced the ability of NGF and cAMP, but not EGF, to activate the transcription factor Elk-1, reduced the induction of both immediate early and late genes after NGF treatment, and blocked the nuclear translocation of ERK1 induced by NGF. We propose that PKA is an important contributor to the activation of ERK1 by NGF and is required for maximal induction of gene expression by NGF.
引用
收藏
页码:8240 / 8247
页数:8
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