...
首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Excitotoxic and apoptotic neuronal death induce different patterns of glial activation in vitro.
【24h】

Excitotoxic and apoptotic neuronal death induce different patterns of glial activation in vitro.

机译:兴奋性和凋亡性神经元死亡在体外诱导神经胶质活化的不同模式。

获取原文
获取原文并翻译 | 示例

摘要

Abstract We have studied glial activation in rat cerebellar neuronal-glial cultures after inducing neuronal death using various stimuli. Cultures were exposed to 100 microm glutamate for 20 min, which induces excitotoxic neuronal death, or to potassium/serum deprivation, which induces apoptosis of granule neurons. We evaluated alterations in several parameters related to glial activation: nuclear factor-kappaB activation, nitric oxide and tumour necrosis factor-alpha production, which are associated with a pro-inflammatory response, glial proliferation and phagocytic activity. Although the two experimental models of neuronal damage resulted in the death of most neuronal cells within 24 h, differences were observed in the response of the various glial parameters evaluated. While nitric oxide production was not detected in any case, tumour necrosis factor-alpha production, nuclear factor-kappaB activation and glial proliferation were only induced in the presence of excitotoxic neuronal death. However, phagocytosis was induced in both cases, although earlier in the case of apoptotic neuronal death. These results show that glial cells respond to excitotoxic neuronal death with an inflammatory response associated with proliferation and phagocytosis. In contrast, whilst glial cells do not produce pro-inflammatory molecules in the presence of apoptotic neuronal death, phagocytic activity is rapidly induced.
机译:摘要我们研究了在大鼠小脑神经胶质细胞培养物中神经胶质的激活,它通过各种刺激诱导神经元死亡。将培养物暴露于100微米谷氨酸盐20分钟,这会引起兴奋性毒性神经元死亡,或者暴露于钾/血清剥夺,这会导致颗粒神经元凋亡。我们评估了与神经胶质细胞活化相关的几个参数的变化:核因子-κB活化,一氧化氮和肿瘤坏死因子-α的产生,它们与促炎反应,神经胶质细胞增殖和吞噬活性相关。尽管两种神经元损伤的实验模型导致大多数神经元细胞在24小时内死亡,但在评估的各种神经胶质参数的反应中观察到差异。虽然在任何情况下均未检测到一氧化氮的产生,但仅在存在兴奋性毒性神经元死亡的情况下才诱导肿瘤坏死因子-α的产生,核因子-κB的活化和神经胶质增生。然而,尽管在凋亡神经元死亡的情况下更早,但在这两种情况下都诱导了吞噬作用。这些结果表明,神经胶质细胞以与增殖和吞噬作用有关的炎症反应对兴奋性神经元死亡作出反应。相反,尽管在凋亡神经元死亡的存在下神经胶质细胞不产生促炎分子,但是吞噬活性被迅速诱导。

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