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鸡胚脊髓培养运动神经元对脑源性神经营养因子、神经营养素3和神经营养素4/5产生存活反应,但对神经生长因子不产生存活反应。

Development of survival responsiveness to brain-derived neurotrophic factor, neurotrophin 3 and neurotrophin 4/5, but not to nerve growth factor, in cultured motoneurons from chick embryo spinal cord.

作者信息

Becker E, Soler R M, Yuste V J, Giné E, Sanz-Rodríguez C, Egea J, Martín-Zanca D, Comella J X

机构信息

Instituto de Microbiología Bioquímica, Departamento de Microbiología y Genética, Consejo Superior de Investigaciones Científicas-Universidad de Salamanca, 37007 Salamanca, Spain.

出版信息

J Neurosci. 1998 Oct 1;18(19):7903-11. doi: 10.1523/JNEUROSCI.18-19-07903.1998.

Abstract

During embryonic development, most neuronal populations undergo a process usually referred to as naturally occurring neuronal death. For motoneurons (MTNs) of the lumbar spinal cord of chick embryos, this process takes place in a well defined period of time, between embryonic days 6 and 10 (E6-E10). Neurotrophins (NTs) are the best characterized family of neurotrophic factors and exert their effects through activation of their specific Trk receptors. In vitro and in vivo studies have demonstrated that rodent motoneurons survive in response to BDNF, NT3, and NT4/5. In contrast, the trophic dependencies of chicken motoneurons have been difficult to elucidate, and various apparently conflicting reports have been published. In the present study, we describe how freshly isolated motoneurons from E5.5 chick embryos did not respond to any neurotrophin in vitro. Yet, because motoneurons were maintained alive in culture in the presence of muscle extract, they developed a delayed specific survival response to BDNF, NT3, and NT4/5 that is clearly dose-dependent, reaching saturation at doses of 100 pg/ml. This trophic response correlated with increasing expression of the corresponding functional receptors TrkB and TrkC. Moreover, TrkB receptor is able to become autophosphorylated and to activate classical intracellular signaling pathways such as the extracellular signal-regulated protein kinase when it is stimulated with its cognate ligand BDNF. Therefore, our results reconcile the reported differences between in vivo and in vitro studies on the ability of chicken MTNs to respond to some members of the neurotrophin family of trophic factors.

摘要

在胚胎发育过程中,大多数神经元群体都会经历一个通常被称为自然发生的神经元死亡的过程。对于鸡胚腰脊髓的运动神经元(MTNs),这个过程发生在一个明确的时间段内,即胚胎第6天到第10天(E6 - E10)。神经营养因子(NTs)是最具特征的神经营养因子家族,通过激活其特定的Trk受体发挥作用。体外和体内研究表明,啮齿动物的运动神经元对BDNF、NT3和NT4/5有反应而存活。相比之下,鸡运动神经元的营养依赖性一直难以阐明,并且已经发表了各种明显相互矛盾的报告。在本研究中,我们描述了从E5.5鸡胚中新鲜分离的运动神经元在体外对任何神经营养因子都没有反应。然而,由于运动神经元在肌肉提取物存在的情况下在培养中保持存活,它们对BDNF、NT3和NT4/5产生了延迟的特异性存活反应,这种反应明显呈剂量依赖性,在100 pg/ml的剂量下达到饱和。这种营养反应与相应功能性受体TrkB和TrkC的表达增加相关。此外,当TrkB受体被其同源配体BDNF刺激时,它能够发生自磷酸化并激活经典的细胞内信号通路,如细胞外信号调节蛋白激酶。因此,我们的结果调和了关于鸡MTNs对神经营养因子家族某些成员反应能力的体内和体外研究中报道的差异。

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