Development of Retinal Receptive Fields

视网膜感受野的发育

• 批准号: 6801563
• 负责人: NORBERTO M GRZYWACZ
• 金额: $ 36.2万
• 依托单位: UNIVERSITY OF SOUTHERN CALIFORNIA
• 依托单位国家: 美国
• 财政年份: 1996
• 资助国家: 美国
• 起止时间: 1996-12-01 至 2007-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6801563
• 关键词: Chelonia; brain electrical activity; calcium indicator; cell growth regulation; computer simulation; dark adaptation; dendrites; developmental neurobiology; electrophysiology; fluorescence microscopy; imaging /visualization /scanning; mathematical model; neostigmine; neural information processing; neural plasticity; neurons; retinal ganglion; synapses; visual fields; visual pathways; visual phototransduction; visual stimulus

DESCRIPTION (provided by applicant): An important property of visual neurons is their receptive-field size. One long-term goal of the proposed research is to understand the developmental mechanisms controlling the growth of retinal receptive fields. We recently established that one such mechanism depends on the spontaneous waves of activity that sweep developing retinas. Four hypotheses for this mechanism involve dendritic-tree growth, optimization of receptive-field size, critical period for growth, and inter-cell competition. We will test these hypotheses in the turtle retina with four aims: 1) We will use intracellular recordings and dendritic staining to test whether spontaneous waves cause receptive fields of ganglion cells to grow by enlarging their dendritic trees. 2) Turtles will be reared in abnormal light environments to test through extracellular recordings whether receptive fields grow to a size optimized to average out noise, while not over-smoothing the image. 3) Ca2+ fluorescence will help us map the waves and ask how light affects them. 4) We will test whether receptive-field growth stops because of a critical period or of an inter-cell competition by increasing the intensity of dark-reared waves though the retinal implantation of drug-laced Elvax. This study could help understand several developmental pathologies affecting ganglion cells. These pathologies include retinopathy of prematurity, retinal degeneration, refsum disease, Leber hereditary optic neuropathy, optic-nerve hypoplasia, and drusen of the optic disk. Besides understanding pathologies, unraveling ganglion-cell plasticity may help with a promising technique for one of their cures, namely, retinal transplantation. In such a transplantation, cells must "self-organize" as during development.

描述（由申请人提供）：视觉神经元的一个重要特性是其感受野大小。这项研究的一个长期目标是了解控制视网膜感受野生长的发育机制。我们最近发现，其中一种机制依赖于扫描发育中视网膜的自发活动波。这一机制的四个假说涉及树状生长，最佳化的感受野大小，生长的关键时期，和细胞间的竞争。我们将在海龟视网膜上测试这些假设，目标有四个： 1)我们将使用细胞内记录和树突染色来测试自发波是否通过扩大树突树而导致神经节细胞的感受野生长。 2)海龟将在异常光环境中饲养，通过细胞外记录测试感受野是否生长到优化的大小，以平均噪音，同时不会过度平滑图像。 3)Ca2+荧光将帮助我们绘制波，并询问光如何影响它们。 4)我们将测试感受野生长是否因为关键期或细胞间竞争而停止，方法是通过视网膜植入药物掺杂的Elvax来增加暗饲养波的强度。 这项研究可以帮助了解影响神经节细胞的几种发育病理学。这些病理包括早产儿视网膜病变、视网膜变性、视网膜变性、Leber遗传性视神经病变、视神经发育不全和视盘玻璃疣。除了了解病理，解开神经节细胞可塑性可能有助于一个有前途的技术，为他们的治疗之一，即视网膜移植。在这样的移植中，细胞必须像在发育期间一样“自我组织”。