Suppr超能文献

神经营养因子反应需要一种糖基磷脂酰肌醇连接受体和Ret受体酪氨酸激酶。

Neurturin responsiveness requires a GPI-linked receptor and the Ret receptor tyrosine kinase.

作者信息

Buj-Bello A, Adu J, Piñón L G, Horton A, Thompson J, Rosenthal A, Chinchetru M, Buchman V L, Davies A M

机构信息

School of Biological and Medical Sciences, University of St Andrews, Fife, UK.

出版信息

Nature. 1997 Jun 12;387(6634):721-4. doi: 10.1038/42729.

Abstract

Neurturin (NTN) is a recently identified homologue of glial-cell-line-derived neurotrophic factor (GDNF). Both factors promote the survival of a variety of neurons, and GDNF is required for the development of the enteric nervous system and kidney. GDNF signals through a receptor complex consisting of the receptor tyrosine kinase Ret and a glycosyl-phosphatidylinositol (GPI)-linked receptor termed GDNFR-alpha. Here we report the cloning of a new GPI-linked receptor termed NTNR-alpha that is homologous with GDNFR-alpha and is widely expressed in the nervous system and other tissues. By using microinjection to introduce expression plasmids into neurons, we show that coexpression of NTNR-alpha with Ret confers a survival response to neurturin but not GDNF, and that coexpression of GDNFR-alpha with Ret confers a survival response to GDNF but not neurturin. Our findings indicate that GDNF and neurturin promote neuronal survival by signalling through similar multicomponent receptors that consist of a common receptor tyrosine kinase and a member of a GPI-linked family of receptors that determines ligand specificity.

摘要

神经营养因子(NTN)是最近发现的胶质细胞源性神经营养因子(GDNF)的同源物。这两种因子都能促进多种神经元的存活,并且GDNF是肠神经系统和肾脏发育所必需的。GDNF通过由受体酪氨酸激酶Ret和一种称为GDNFR-α的糖基磷脂酰肌醇(GPI)连接受体组成的受体复合物发出信号。在此,我们报告了一种新的GPI连接受体NTNR-α的克隆,它与GDNFR-α同源,在神经系统和其他组织中广泛表达。通过显微注射将表达质粒导入神经元,我们发现NTNR-α与Ret共表达赋予神经元对神经营养因子而非GDNF的存活反应,而GDNFR-α与Ret共表达赋予神经元对GDNF而非神经营养因子的存活反应。我们的研究结果表明,GDNF和神经营养因子通过由共同的受体酪氨酸激酶和决定配体特异性的GPI连接受体家族成员组成的相似多组分受体发出信号来促进神经元存活。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验