Exploring plasticity of the adult visual system using viral gene delivery

利用病毒基因传递探索成人视觉系统的可塑性

• 批准号: 7384422
• 负责人: MAUREEN E NEITZ
• 金额: $ 37.12万
• 依托单位: MEDICAL COLLEGE OF WISCONSIN
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-04-01 至 2012-02-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7384422
• 关键词: Adult; Age-Months; Animals; Appearance; Applications Grants; Area; Behavior; Behavior Control; Biological Models; Birth; Blindness; Canis familiaris; Color; Color Visions; Data; Development; Discrimination; Electroretinography; Eye; Felis catus; Functional disorder; Gene Delivery; Genes; Gerbils; Goals; Inherited; Lateral Geniculate Body; Leber' s amaurosis; Light; Literature; Mediating; Monitor; Mutation; Neuronal Plasticity; Performance; Personal Satisfaction; Photic Stimulation; Photons; Photoreceptors; Phototransduction; Pigments; Plastics; RPE65 protein; Research; Research Personnel; Retina; Retinal; Retinal Cone; Retinal Degeneration; Saimiri; Sensory; Signal Transduction; Sorting - Cell Movement; Testing; Therapeutic Intervention; Viral; Vision; Visual Cortex; Visual system structure; Work; behavior test; blind; critical developmental period; design; functional loss; gain of function; gene therapy; neglect; object perception; programs; relating to nervous system; research study; retinal prosthesis; viral gene delivery; visual deprivation

DESCRIPTION (provided by applicant): The long-term goals of the work proposed in this grant application are to study neural plasticity of the adult mammalian visual system by adding new sensory input. Experiments that enhance rather than ablate sensory input offer a new avenue of research for answering fundamental questions about the plasticity of the adult visual system and have important implications for the rational design of gene therapy and retinal prostheses. We have chosen red-green color vision as a model system in which gain of function can be monitored quantitatively at the level of the retina using the electroretinogram and at the level of the visual cortex with behavioral tests of color vision. As a first step toward achieving our long term goals, we propose two specific aims. Specific Aim 1. To determine whether adding a third cone type via viral mediated delivery of a photopigment gene to the retina in a dichromatic adult squirrel monkey can expand his sensory capacity and change color vision behavior from dichromatic to trichromatic. Specific Aim 2. To determine whether expressing a long-wavelength sensitive pigment gene in a subset of UV cones via viral mediated gene delivery to the gerbil retina can expand the gerbil's color vision capacity to include making color discriminations in the red-green region of the spectrum.

描述（由申请人提供）：这项资助申请中提出的工作的长期目标是通过增加新的感觉输入来研究成年哺乳动物视觉系统的神经可塑性。增强而不是消融感觉输入的实验为回答成人视觉系统可塑性的基本问题提供了一条新的研究途径，并对基因治疗和视网膜假体的合理设计具有重要意义。我们选择了红-绿色觉作为模型系统，在该模型系统中，可以使用视网膜电图在视网膜水平上和使用色觉的行为测试在视觉皮层水平上定量地监测功能的获得。作为实现我们长期目标的第一步，我们提出了两个具体目标。 具体目标1。为了确定通过病毒介导的向二色视成年松鼠猴的视网膜递送一种新色素基因是否可以扩大其感觉能力并将色觉行为从二色视改变为三色视。 具体目标2。为了确定是否通过病毒介导的基因传递到沙鼠视网膜的紫外线锥细胞的子集中表达长波长敏感的色素基因可以扩大沙鼠的色觉能力，包括在光谱的红-绿区域进行颜色辨别。