Subcellular Pathways of Internalized Neurotrophics

神经营养因子是神经元之间通讯的信使。它们调节神经元的分化和功能。内化、胞内转运、信号转导和最终降解是营养信号传导的基本步骤。最近的研究表明，内化的神经营养因子可以分为降解或回收途径。该应用程序的主要目的是阐明如何内化的神经营养因子被分为不同的细胞内途径。这项研究将主要在波兰的Nencki研究所进行，作为NIH资助# RO 1 EY 12841的延伸。拟议的研究将利用鸡胚发育中的视觉系统作为独特的体内模型系统，该系统允许将放射性标记的营养因子引入隔室并定量细胞内途径。实验将集中在不同的亚细胞通路的比较后，神经营养因子的树突（视网膜神经节细胞）和后内化专门由轴突末梢（峡部视神经元）。这些实验将显示摄取途径（树突与轴突）如何影响随后的信号传导和降解途径。超微结构水平的放射自显影将用于确定神经营养因子的亚细胞分布。将比较神经营养因子之间的分布特征。体内转运的神经营养因子的受体结合将通过与受体特异性抗体的交联和免疫沉淀来测定。细胞器中，内化的神经营养素积累和他们的途径和亚细胞的目的地将进行比较和实验操作的竞争与异源神经营养素和酪氨酸激酶受体的失活。分子，药理学和超微结构的方法相结合，将使我们能够回答有关贩运的神经营养因子，这是至关重要的了解这些因素如何可能调节不同的神经元存活和突触可塑性的事件的问题。神经退行性疾病与营养支持缺陷有关。有关神经营养因子的正常运输、分类和再循环的知识将有助于我们了解病理条件以及外源性神经营养因子如何可用作治疗剂。

Neurotrophic factors are messengers in the communication between neurons. They regulate neuronal differentiation and function. Internalization, intracellular transport, signal transduction and eventual degradation are essential steps in trophic signaling. Recent studies have shown that internalized neurotrophins can be sorted into either degradative or recycling pathways. The application's central aim is to elucidate how internalized neurotrophins are sorted into distinct intracellular pathways. This research will be done primarily at the Nencki Institute in Poland as an extension of NIH grant # RO 1 EY 12841. The proposed studies will utilize the developing visual system of chick embryos as a unique invivo model system which allows the introduction of radiolabeled trophic factors into a compartment and the quantification of intracellular pathways. Experiments will focus on the comparison of different subcellular pathways after internalization of neurotrophins by dendrites (retinal ganglion cells) and after internalization exclusively by axon terminals (isthmo-optic neurons). These experiments will show how the route of uptake (dendritic vs. axonal) influences the subsequent signaling and degradation pathways. Autoradiography at the ultrastructural level will be used to identify the subcellular distribution of neurotrophins. Distribution profiles will be compared between neurotrophins. Receptor binding of invivo- transported neurotrophins will be determined by crosslinking and immunoprecipitation with receptor-specific antibodies. The organelles in which internalized neurotrophins accumulate and their pathways and subcellular destinations will be compared and experimentally manipulated by competition with heterologous neurotrophins and inactivation of tyrosine kinase receptors. The combination of molecular, pharmacological and ultrastructural approaches will allow us to answer questions about trafficking of neurotrophins which are crucial to an understanding of how these factors may regulate events as diverse as neuronal survival and synaptic plasticity. Neurodegenerative diseases have been related to deficits in trophic support. Knowledge about the normal trafficking, sorting and recycling of neurotrophic factors will help us to understand pathologic conditions and how exogenous neurotrophins may be used as therapeutic agents.