Sema3D Role in Retinal Axon Guidance and Cell Migration

Sema3D 在视网膜轴突引导和细胞迁移中的作用

• 批准号: 6751562
• 负责人: MARY C HALLORAN
• 金额: $ 27.23万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-08-01 至 2007-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6751562
• 关键词: axon; cell growth regulation; cell migration; cell motility; developmental neurobiology; embryo /fetus; gene expression; genetically modified animals; glycoproteins; growth cones; neural crest; neuronal guidance; receptor expression; retina; transfection; video microscopy; zebrafish

DESCRIPTION (provided by applicant): Semaphorins have been implicated in the regulation of axon pathfinding, sometimes acting as inhibitory guidance molecules, and other times attractive. An understanding of the complex processes involved in promoting and inhibiting axon growth will be crucial for understanding both diseases of neural development, and the conditions under which axon regeneration after injury can occur. Semaphorins also are thought to play a role in controlling the related processes of cell migration during development, metastasis and invasive growth. Cranial neural crest cells migrate from the neural tube to form craniofacial structures and peripheral nervous system. Errors in migration of cranial neural crest during development underlies many birth defects in craniofacial structure. An investigation of the mechanisms by which semaphorins control neural crest migration will provide insight into craniofacial development, and perhaps also general mechanisms of invasive growth involved in cancer progression.The aim of this application is to understand the in vivo function of one semaphorin, Sema3D, in guiding retinotectal axon pathfinding and neural crest cell migration in the developing zebrafish. Sema3D's role in guiding retinal axons across the midline and in topographic mapping onto the tectum will be investigated. In addition, Sema3D's role in controlling cell motility will be investigated to test the hypotheses that Sema3D induces the onset of neural crest migration, and/or maintains separation of migrating neural crest streams. Our strategy is to examine effects of both Sema3D ectopic expression and Sema3D loss-of-function on the development of these systems, and on dynamic behaviors of living growth cones and migrating neural crest cells in vivo. The zebrafish embryo is ideally suited to the combination of approaches we have developed. With transgenic zebrafish, Sema3D can be misexpressed in select cells at any desired developmental stage. In addition, Sema3D function can be disrupted with antisense or dominant negative methods. Time-lapse microscopy allows direct visualization of the responses of living growth cones or migrating cells in the embryo. Thus the proposed experiments will likely provide novel insights into how semaphorins regulate retinal axon development and neural crest cell migration within the complex in vivo environment.

描述（由申请人提供）：信号蛋白与轴突寻路的调节有关，有时充当抑制性引导分子，有时则具有吸引力。了解促进和抑制轴突生长的复杂过程对于理解神经发育疾病以及损伤后轴突再生的条件至关重要。信号蛋白还被认为在控制发育、转移和侵袭性生长过程中细胞迁移的相关过程中发挥作用。颅神经嵴细胞从神经管迁移形成颅面结构和周围神经系统。发育过程中颅神经嵴迁移错误是颅面结构许多出生缺陷的基础。对信号蛋白控制神经嵴迁移机制的研究将有助于深入了解颅面发育，或许还可以了解参与癌症进展的侵袭性生长的一般机制。本应用的目的是了解信号蛋白 Sema3D 在指导发育中的斑马鱼视网膜顶盖轴突寻路和神经嵴细胞迁移方面的体内功能。我们将研究 Sema3D 在引导视网膜轴突穿过中线以及在顶盖上进行地形测绘方面的作用。此外，还将研究 Sema3D 在控制细胞运动中的作用，以测试 Sema3D 诱导神经嵴迁移开始和/或维持迁移神经嵴流分离的假设。我们的策略是检查 Sema3D 异位表达和 Sema3D 功能丧失对这些系统发育的影响，以及对体内活生长锥和迁移神经嵴细胞动态行为的影响。斑马鱼胚胎非常适合我们开发的方法的组合。对于转基因斑马鱼，Sema3D 可以在任何所需发育阶段的选定细胞中错误表达。此外，Sema3D 功能可以通过反义或显性失活方法来破坏。延时显微镜可以直接观察胚胎中活生长锥或迁移细胞的反应。因此，所提出的实验可能会为信号蛋白如何在复杂的体内环境中调节视网膜轴突发育和神经嵴细胞迁移提供新的见解。