...
【24h】

Differential regulation of BDNF and NT-3 mRNA levels in primary cultures of rat cerebellar neurons.

机译:大鼠小脑神经元原代培养物中BDNF和NT-3 mRNA水平的差异调节。

获取原文
获取原文并翻译 | 示例
           

摘要

Reciprocal developmental patterns of expression for BDNF and NT-3 have been observed in several neuronal types, including cerebellar granule neurons: NT3 mRNA level decreased and BDNF mRNA increased in granule cells concomitantly with their migration and maturation. In the present study we analysed cultured cerebellar granule neurons prepared from postnatal rat cerebellum, a model system widely used for studies on the maturation and survival of these neurons. We show that chronic depolarization, induced by 25 mM K+ in the culture medium, is able to sustain a persistent increase of BDNF expression in cerebellar granule neurons. It has been suggested that chronic depolarization in vitro mimics the effect of the earliest afferent inputs received by granule cells in vivo: on this basis we suggest that the beginning of neuronal activity in differentiated granule neurons may represent one of the signals that trigger the developmental increase in BDNF expression. Interestingly, we observed that up-regulation of BDNF expression in vitro is accompanied by a dramatic decrease of NT-3 expression: a differential regulation that is highly reminiscent of the reciprocal developmental patterns of expression observed in vivo for BDNF and NT-3. Another point raised by the present results is the possible role of BDNF, acting in an autocrine or paracrine manner, in the trophic effect of high potassium concentration. Indeed, repeated additions of BDNF to the culture medium have a trophic effect on cerebellar granule neurons but reproduce only partially the survival effect observed with 25 mM K+ conditions, suggesting that the increased expression of BDNF is not the only mechanism responsible for the trophic effects of high potassium. In conclusion we show the existence of a reciprocal regulation of BDNF and NT-3 expression in cultured cerebellar granule neurons and we propose that this culture system could represent an in vitro model for the study of the molecular mechanisms underlying the developmental regulation of these neurotrophins in cerebellum.
机译:在包括小脑颗粒神经元在内的几种神经元类型中已经观察到BDNF和NT-3表达的相互发展模式:颗粒细胞中NT3 mRNA的水平下降,而BDNF mRNA的水平上升则伴随着它们的迁移和成熟。在本研究中,我们分析了从产后大鼠小脑制备的培养的小脑颗粒神经元,该模型系统广泛用于研究这些神经元的成熟和存活。我们显示,由培养基中的25 mM K +引起的慢性去极化能够维持小脑颗粒神经元中BDNF表达的持续增加。有人提出体外慢性去极化模拟了颗粒细胞在体内接受的最早传入输入的作用:在此基础上,我们建议分化的颗粒神经元中神经元活性的开始可能代表触发发育增加的信号之一。在BDNF表达中。有趣的是,我们观察到BDNF在体外的表达上调伴随着NT-3表达的急剧下降:这种差异性调节高度让人联想到在体内针对BDNF和NT-3的表达的相互发展模式。本研究结果提出的另一点是,BDNF在高钾浓度的营养作用中可能以自分泌或旁分泌方式起作用。确实,向培养基中反复添加BDNF对小脑颗粒神经元有营养作用,但仅部分复制了在25 mM K +条件下观察到的存活作用,这表明BDNF表达的增加并不是引起小脑颗粒营养作用的唯一机制。高钾。总之,我们证明了在培养的小脑颗粒神经元中存在BDNF和NT-3表达的相互调节,并且我们建议该培养系统可以代表体外模型,用于研究这些神经营养蛋白在体内调节发育的分子机制。小脑。

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