首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Expression of c-fos, c-jun, and c-jun N-terminal kinase (JNK) in a developmental model of induced apoptotic death in neurons of the substantia nigra.
【24h】

Expression of c-fos, c-jun, and c-jun N-terminal kinase (JNK) in a developmental model of induced apoptotic death in neurons of the substantia nigra.

机译:c-fos,c-jun和c-jun N末端激酶(JNK)在黑质黑质神经元诱导的细胞凋亡死亡的发育模型中的表达。

获取原文
获取原文并翻译 | 示例
           

摘要

The transcription factors c-fos and c-jun have been proposed to play a role in the initiation of programmed cell death in neurons. We have shown that programmed cell death, with the morphology of apoptosis, occurs in dopamine neurons of the substantia nigra (SN) during normal postnatal development and that this death event can be induced by early striatal target injury. We have investigated the relationship between c-fos and c-jun protein expression and induced death in neurons of the SN. Although c-fos is induced, it is unlikely to play a role in cell death, because its expression is not well correlated with apoptotic death either temporally or at a cellular level. Expression of c-jun, however, is both temporally and regionally correlated with induction of death, and, at a cellular level, it colocalizes with apoptotic morphology. The increased expression of c-jun is likely to be functionally significant, because it is associated with increased c-jun N-terminal kinase (JNK) and phosphorylated c-jun expression. JNK expression also colocalizes with apoptotic morphology. We conclude that c-jun is likely to play a role in the initiation of apoptotic cell death in these neurons.
机译:已经提出转录因子c-fos和c-jun在神经元中程序性细胞死亡的引发中起作用。我们已经显示,在正常的产后发育过程中,黑质(SN)的多巴胺神经元中发生了程序性细胞死亡,具有凋亡形态,并且这种死亡事件可能是由早期纹状体靶损伤引起的。我们已经研究了c-fos和c-jun蛋白表达与SN神经元诱导的死亡之间的关系。尽管诱导了c-fos,但它不太可能在细胞死亡中起作用,因为其表达在时间或细胞水平上均与凋亡性死亡没有很好的相关性。然而,c-jun的表达在时间和区域上均与诱导死亡相关,并且在细胞水平上与凋亡形态共定位。 c-jun表达的增加可能在功能上很重要,因为它与c-jun N末端激酶(JNK)和磷酸化c-jun表达的增加有关。 JNK表达也与凋亡形态共定位。我们得出结论,c-jun可能在这些神经元的凋亡细胞死亡的起始中发挥作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号