首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Activation of cAMP-response-element-binding protein (CREB) after focal cerebral ischemia stimulates neurogenesis in the adult dentate gyrus.
【24h】

Activation of cAMP-response-element-binding protein (CREB) after focal cerebral ischemia stimulates neurogenesis in the adult dentate gyrus.

机译:局灶性脑缺血后cAMP反应元件结合蛋白(CREB)的激活刺激了成年齿状回的神经发生。

获取原文
获取原文并翻译 | 示例
           

摘要

New neurons are generated in adult mammalians and may contribute to repairing the brain after injury. Here, we show that the number of new neurons in the dentate gyrus of adult rats increased in cerebral ischemic stroke and correlated with activation of the cAMP-response-element-binding protein (CREB). Inhibition of endogenous CREB by expression of a dominant-negative mutant of CREB (CREB-S133A or CREB-R287L) blocked ischemia-induced neurogenesis in the dentate gyrus of adult rats, whereas expression of constitutively active CREB, VP16-CREB, increased the number of new neurons. Thus, our findings provide roles and regulatory mechanisms for CREB in adult neurogenesis and possibly suggest a practical strategy for replacing dead neurons in brain injury.
机译:新的神经元在成年哺乳动物中产生,并可能在受伤后有助于大脑的修复。在这里,我们显示成年大鼠的齿状回中新的神经元的数目在脑缺血性中风中增加,并且与cAMP反应元件结合蛋白(CREB)的激活相关。通过表达CREB的显性负突变体(CREB-S133A或CREB-R287L)抑制内源性CREB可以阻断成年大鼠齿状回中缺血诱导的神经发生,而组成型活性CREB ​​VP16-CREB的表达增加了数量新的神经元。因此,我们的发现提供了CREB在成人神经发生中的作用和调控机制,并可能提出了替代脑损伤中死亡神经元的实用策略。

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