Antiapoptotic role of the p38 mitogen-activated protein kinase-myocyte enhancer factor 2 transcription factor pathway during neuronal differentiation

被引:173
作者
Okamoto, S
Krainc, D
Sherman, K
Lipton, SA
机构
[1] Burnham Inst, Ctr Neurosci & Aging, La Jolla, CA 92037 USA
[2] Brigham & Womens Hosp, Cerebrovasc & Neurosci Res Inst, Boston, MA 02115 USA
[3] Childrens Hosp, Div Neurosci, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
关键词
D O I
10.1073/pnas.130502697
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Myocyte enhancer factor 2 (MEF2) is in the MADS (MCM1-agamous-deficiens-serum response factor) family of transcription factors. Although MEF2 is known as a myogenic factor, the expression pattern of the MEF2 family of genes (MEF2A-D) in developing brain also suggests a role in neurogenesis. Here we show that transfection with MEF2C. the predominant form in mammalian cerebral cortex, induces a mixed neuronal/myogenic phenotype in undifferentiated P19 precursor cells. During retinoic acid-induced neurogenesis of these cells, a dominant negative form of MEF2 enhances apoptosis but does not affect cell division. The mitogen-activated protein kinase p38 alpha activates MEF2C. Dominant negative p38 alpha also enhances apoptotic death of differentiating neurons, but these cells can be rescued from apoptosis by coexpression of constitutively active MEF2C. These findings suggest that the p38 alpha/MEF2 pathway prevents cell death during neuronal differentiation.
引用
收藏
页码:7561 / 7566
页数:6
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