ERK5 activation of MEF2-mediated gene expression plays a critical role in BDNF-promoted survival of developing but not mature cortical neurons

被引:140
作者
Liu, LD
Cavanaugh, JE
Wang, YP
Sakagami, H
Mao, ZX
Xia, ZG [1 ]
机构
[1] Univ Washington, Dept Environm Hlth, Seattle, WA 98195 USA
[2] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
[3] Univ Washington, Grad Program Neurobiol & Behav, Seattle, WA 98195 USA
[4] Univ Washington, Grad Program Mol & Cell Biol, Seattle, WA 98195 USA
[5] Rhode Isl Hosp, Dept Med, Liver Res Ctr, Providence, RI 02903 USA
[6] Brown Univ Med, Providence, RI 02903 USA
关键词
D O I
10.1073/pnas.1332804100
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
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 PO. Furthermore, expression of a dominant-negative ERK5 induced apoptosis in E17 but not PO 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.
引用
收藏
页码:8532 / 8537
页数:6
相关论文
共 48 条
[1]   Transcriptional control of muscle development by myocyte enhancer factor-2 (MEF2) proteins [J].
Black, BL ;
Olson, EN .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 :167-196
[2]  
Casaccia-Bonnefil P, 1999, ADV EXP MED BIOL, V468, P275
[3]  
Castellino Alexander M., 1996, Cytokine and Growth Factor Reviews, V7, P297, DOI 10.1016/S1359-6101(96)00038-X
[4]   Differential regulation of mitogen-activated protein kinases ERK1/2 and ERK5 by neurotrophins, neuronal activity, and cAMP in neurons [J].
Cavanaugh, JE ;
Ham, J ;
Hetman, M ;
Poser, S ;
Yan, C ;
Xia, ZG .
JOURNAL OF NEUROSCIENCE, 2001, 21 (02) :434-443
[5]   HUMAN CYTOMEGALOVIRUS-IE1 TRANSACTIVATES THE ALPHA-PROMOTER-ENHANCER VIA AN 18-BASE-PAIR REPEAT ELEMENT [J].
CHERRINGTON, JM ;
MOCARSKI, ES .
JOURNAL OF VIROLOGY, 1989, 63 (03) :1435-1440
[6]   ACTIVATION OF MAP KINASE KINASE IS NECESSARY AND SUFFICIENT FOR PC12 DIFFERENTIATION AND FOR TRANSFORMATION OF NIH 3T3 CELLS [J].
COWLEY, S ;
PATERSON, H ;
KEMP, P ;
MARSHALL, CJ .
CELL, 1994, 77 (06) :841-852
[7]  
Datta SR, 1998, HORM SIGNALING, V1, P257
[8]   Extracellular signal regulated kinase 5 (ERK5) is required for the differentiation of muscle cells [J].
Dinev, D ;
Jordan, BWA ;
Neufeld, B ;
Lee, JD ;
Lindemann, D ;
Rapp, UR ;
Ludwig, S .
EMBO REPORTS, 2001, 2 (09) :829-834
[9]   Granulocyte colony-stimulating factor induces Erk5 activation, which is differentially regulated by protein-tyrosine kinases and protein kinase C - Regulation of cell proliferation and survival [J].
Dong, F ;
Gutkind, JS ;
Larner, AC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (14) :10811-10816
[10]   Identification of substrates and regulators of mitogen-activated protein kinase ERK5 using chimeric protein kinases [J].
English, JM ;
Pearson, G ;
Baer, R ;
Cobb, MH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (07) :3854-3860