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乙醇通过一种蛋白激酶C依赖性机制增强丝裂原活化蛋白激酶的生长因子激活作用。

Ethanol enhances growth factor activation of mitogen-activated protein kinases by a protein kinase C-dependent mechanism.

作者信息

Roivainen R, Hundle B, Messing R O

机构信息

Department of Neurology, University of California, San Francisco 94110.

出版信息

Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):1891-5. doi: 10.1073/pnas.92.6.1891.

Abstract

Excessive alcohol consumption alters neuronal growth and causes striking elongation of axons and dendrites in several brain regions. This could result from increased sensitivity to neurotrophic factors, since ethanol markedly enhances nerve growth factor (NGF)- and basic fibroblast growth factor (bFGF)-stimulated neurite outgrowth in the neural cell line PC12. The mechanism by which ethanol enhances growth factor responses was investigated by examining activation of mitogen-activated protein kinases (MAP kinases), a key event in growth factor signaling. Ethanol (100 mM) increased NGF- and bFGF-induced activation of MAP kinases. This increase, like ethanol-induced increases in neurite outgrowth, was prevented by down regulation of beta, delta, and epsilon protein kinase C (PKC) isozymes. Since chronic ethanol exposure specifically upregulates delta and epsilon PKC, these findings suggest that ethanol promotes neurite growth by enhancing growth factor signal transduction through a delta or epsilon PKC-regulated pathway.

摘要

过量饮酒会改变神经元的生长,并导致几个脑区的轴突和树突显著延长。这可能是由于对神经营养因子的敏感性增加所致,因为乙醇能显著增强神经生长因子(NGF)和碱性成纤维细胞生长因子(bFGF)刺激神经母细胞瘤细胞系PC12中的神经突生长。通过检测丝裂原活化蛋白激酶(MAP激酶)的激活来研究乙醇增强生长因子反应的机制,MAP激酶的激活是生长因子信号传导中的关键事件。乙醇(100 mM)增加了NGF和bFGF诱导的MAP激酶激活。这种增加,就像乙醇诱导的神经突生长增加一样,可通过下调β、δ和ε蛋白激酶C(PKC)同工酶来阻止。由于长期暴露于乙醇会特异性地上调δ和ε PKC,这些发现表明乙醇通过δ或ε PKC调节的途径增强生长因子信号转导来促进神经突生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/080b/42388/cd64d2be758b/pnas01484-0109-a.jpg

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