INTEGRATING SIGNALS GUIDING AXONAL GROWTH AND BRANCHING

整合引导轴突生长和分支的信号

• 批准号: 6243191
• 负责人: SCOTT E FRASER
• 金额: $ 17.23万
• 依托单位: CALIFORNIA INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 1997
• 资助国家: 美国
• 起止时间: 1997-09-01 至 1998-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6243191
• 关键词: Xenopus; alternatives to animals in research; axon; biological signal transduction; cell differentiation; cell growth regulation; chimeric proteins; confocal scanning microscopy; developmental neurobiology; embryo /fetus tissue /cell culture; green fluorescent proteins; growth factor receptors; neuronal guidance; neurotrophic factors; optic nerve; optic tract; receptor expression; retinal ganglion; synaptogenesis; video microscopy

The long term goal of this project is to determine the cues that guide axonal growth, synaptogenesis and synaptic modification in the developing vertebrate brain. Here, we propose to examine in vivo the growth, differentiation and modification of optic nerve axons in the frog Xenopus laevis. The growth and branching of individual optic nerve fibers will be followed as they grow into and branch to form terminal arbors within their primary target, the optic tectum, using low light level video microscopy, laser scanning confocal microscopy and two-photon laser scanning microscopy. The ability to observe identified axons in vivo offers the rare opportunity to experimentally dissect the signals that guide axonal growth in a biologically relevant setting. The experiments will exploit our recent progress in showing that the neurotrophin BDNF is a relevant factor for visual system development in frog. The experiments will extend the previous results, which showed that the changing the levels of BDNF in the target tissue rapidly and dramatically altered the branching pattern of the optic nerve fibers. In particular, the experiments will: -explore the consequences of BDNF-mediated signaling in the retinotectal projection; - determine the interactions between neuronal activity and the action(s) of neurotrophins; - employ fusion proteins to follow the assembly of synaptic specializations. The experiments will extend approaches typically used only in culture by using modern imaging technologies to permit the living, intact nervous system to be studied. As such, they offer a rare glimpse into the dynamics of synaptic patterning and the integration between multiple cues in forming patterned neural networks.

这个项目的长期目标是确定线索， 引导轴突生长、突触发生和突触修饰 正在发育的脊椎动物大脑在这里，我们建议在体内检查 视神经轴突的生长、分化和修饰 非洲爪蟾单个视神经的生长和分支 神经纤维将随着它们的生长而形成分支 终端乔木在其主要目标，视顶盖，使用 微光视频显微镜、激光扫描共聚焦显微镜 和双光子激光扫描显微镜。观察能力 在体内识别轴突提供了难得的机会， 实验性地剖析了在神经元中引导轴突生长的信号， 生物相关的设置。实验将利用我们的 最近的进展表明，神经营养因子BDNF是一个相关的 青蛙视觉系统发育的因素。实验将 扩展了之前的结果，这表明改变 靶组织中的BDNF水平迅速而显著地改变 视神经纤维的分支模式特别是 实验将：-探索BDNF介导的后果 视网膜顶盖投射中的信号; -确定 神经元活动与以下行为之间的相互作用 神经营养素; -采用融合蛋白，以遵循组装 突触特化这些实验将扩展 通常只在培养中使用现代成像技术 以研究活体的完整神经系统。因此，在本发明的一个方面， 它们提供了一个难得的机会来了解突触模式的动态 以及在形成模式化的过程中， 神经网络