...
首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Class A plexin expression in axotomized rubrospinal and facial motoneurons.
【24h】

Class A plexin expression in axotomized rubrospinal and facial motoneurons.

机译:轴突化的脊髓神经节和面部运动神经元中的A类plexin表达。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The semaphorin family of guidance molecules plays a role in many aspects of neural development, and more recently semaphorins have been implicated to contribute to the failure of injured CNS neurons to regenerate. While semaphorin expression patterns after neural injury are partially understood, little is known about the expression of their signal transducing transmembrane receptors, the plexins. Therefore, in this study, we compared the expression patterns of all class A plexins (Plxn-A1, A2, A3, A4) in mouse CNS (rubrospinal) and peripheral nervous system (PNS)-projecting (facial) motoneurons for up to two weeks following axonal injury. Using in situ hybridization, immunohistochemistry, and Western blot analysis, in rubrospinal neurons, Plxn-A1 mRNA and protein and Plxn-A4 expression did not change as a result of injury while Plxn-A2 mRNA increased and Plxn-A3 mRNA was undetectable. In facial motoneurons, Plxn-A1, -A3 and -A4 mRNA expression increased, Plxn-A2 mRNA decreased while Plxn-A1 protein expression did not change following injury. We demonstrate that with the exception of the absence of Plxn-A3 mRNA in rubrospinal neurons, both injured rubrospinal (CNS) and facial (PNS) neurons maintain expression of all plexin A family members tested. Hence, there are distinct expression patterns of the individual plexin-A family members suggesting that regenerating rubrospinal and facial motoneurons have a differential ability to transduce semaphorin signals.
机译:semaphorin家族的指导分子在神经发育的许多方面都发挥着作用,最近,semaphorin被认为与受伤的CNS神经元再生失败有关。虽然对神经损伤后的信号量表达模式有部分了解,但对其信号转导跨膜受体神经丛的表达知之甚少。因此,在这项研究中,我们比较了小鼠中枢神经系统(红松神经)和外周神经系统(PNS)投射(面部)运动神经元中所有两种A类神经丛蛋白(Plxn-A1,A2,A3,A4)的表达模式轴突损伤后几周。使用原位杂交,免疫组化和Western印迹分析,在损伤后的脊髓神经元中,Plxn-A1 mRNA和蛋白以及Plxn-A4表达没有因损伤而改变,而Plxn-A2 mRNA升高而Plxn-A3 mRNA无法检测到。在面部运动神经元中,损伤后Plxn-A1,-A3和-A4 mRNA表达增加,Plxn-A2 mRNA表达降低,而Plxn-A1蛋白表达未改变。我们证明,除了在脊髓神经节神经元中不存在Plxn-A3 mRNA以外,受伤的脊髓神经节(CNS)和面部(PNS)神经元均保持了所有受测的plexin A家族成员的表达。因此,个体plexin-A家族成员存在不同的表达模式,这表明再生红松神经和面部运动神经元具有不同的转导信号量信号的能力。

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