ATF3 enhances c-Jun-mediated neurite sprouting

被引:84
作者
Pearson, AG
Gray, CW
Pearson, JF
Greenwood, JA
During, MJ
Dragunow, M
机构
[1] Univ Auckland, Dept Pharmacol & Clin Pharmacol, Auckland 1, New Zealand
[2] Univ Auckland, Dept Stat, Auckland 1, New Zealand
[3] Univ Auckland, Dept Mol Med, Auckland 1, New Zealand
来源
MOLECULAR BRAIN RESEARCH | 2003年 / 120卷 / 01期
关键词
c-jun; ATF3; axonal regeneration; neurite; PC12; neuro-2a;
D O I
10.1016/j.molbrainres.2003.09.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The AP-1 transcription factor c-Jun is induced in axotomized neurons of the peripheral and central nervous systems, and in both cases upregulation of c-Jun expression has been correlated with axonal regeneration. More recently there has been interest in the c-Jun-related bZIP transcription factor, ATF3, and its function in neurons. ATF3 is also induced in nerve cells in response to axotomy and there is a correlation between increased ATF3 expression and upregulation of c-Jun in surviving neurons. Moreover, c-Jun is able to induce expression of ATF3. We investigated the effect of co-expressing c-Jun and ATF3 in two neuronal-like cell lines to model transcriptional events occurring in axotomized neurons undergoing regeneration. We show that expression of ATF3 with c-Jun significantly enhances c-Jun-mediated neurite sprouting, and that this phenotype is most likely mediated by a physical association of these two transcription factors. Our results suggest that a program of axonal regeneration is initiated when both c-Jun and ATF3 are upregulated in neurons in response to axotomy. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:38 / 45
页数:8
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