Liu Lidong, Cavanaugh Jane E, Wang Yupeng, Sakagami Hiroyuki, Mao Zixu, Xia Zhengui
Department of Environmental Health, University of Washington, Seattle, WA 98195-7234, USA.
Proc Natl Acad Sci U S A. 2003 Jul 8;100(14):8532-7. doi: 10.1073/pnas.1332804100. Epub 2003 Jun 25.
Extracellular signal-regulated kinase 5 (ERK5) is a member of the mitogen-activated protein kinase family whose biological function in the CNS has not been defined. In contrast to ERK1 and ERK2, which are activated by neurotrophins (NTs), cAMP, and neuronal activity in cortical neurons, ERK5 is activated only by NTs. Here, we report that ERK5 expression is high in the brain during early embryonic development but declines as the brain matures to almost undetectable levels by postnatal day (P) 49. Interestingly, expression of a dominant-negative ERK5 blocked brain-derived neurotrophic factor protection against trophic withdrawal in primary cortical neurons cultured from embryonic day (E) 17 but not P0. Furthermore, expression of a dominant-negative ERK5 induced apoptosis in E17 but not P0 cortical neurons maintained in the presence of serum. We also present evidence that ERK5 protection of E17 cortical neurons may be mediated through myocyte enhancer factor 2-induced gene expression. These data suggest that ERK5 activation of myocyte enhancer factor 2-induced gene expression may play an important and novel role in the development of the CNS by mediating NT-promoted survival of embryonic neurons.
细胞外信号调节激酶5(ERK5)是丝裂原活化蛋白激酶家族的成员,其在中枢神经系统中的生物学功能尚未明确。与在皮质神经元中被神经营养因子(NTs)、cAMP和神经元活动激活的ERK1和ERK2不同,ERK5仅被NTs激活。在此,我们报告ERK5在胚胎发育早期大脑中的表达很高,但随着大脑成熟,到出生后第49天(P49)时其表达下降至几乎检测不到的水平。有趣的是,显性负性ERK5的表达阻断了脑源性神经营养因子对从胚胎第17天(E17)而非出生后第0天(P0)培养的原代皮质神经元营养剥夺的保护作用。此外,显性负性ERK5的表达在存在血清的情况下诱导E17而非P0皮质神经元发生凋亡。我们还提供证据表明ERK5对E17皮质神经元的保护作用可能通过肌细胞增强因子2诱导的基因表达介导。这些数据表明,ERK5激活肌细胞增强因子2诱导的基因表达可能通过介导NTs促进胚胎神经元存活,在中枢神经系统发育中发挥重要且新颖的作用。