Functional Imaging of Ganglion Cells in the Living Mammalian Eye

活体哺乳动物眼中神经节细胞的功能成像

• 批准号: 8021616
• 负责人: William H Merigan
• 金额: $ 68.15万
• 依托单位: UNIVERSITY OF ROCHESTER
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-02-01 至 2014-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8021616
• 关键词: Address; Anemia; Animals; Behavioral; Brain; Cell Nucleus; Cells; Collaborations; Dependovirus; Development; Electrophysiology (science); Equus caballus; Eye; Eye Development; Eye Enucleation; Fluorescence; Functional Imaging; Gene Delivery; Grant; Image; Immunologic Deficiency Syndromes; In Vitro; Individual; Injection of therapeutic agent; Institutes; Life; Macaca; Mammals; Maps; Methodology; Methods; Microelectrodes; Monitor; Monkeys; Motion; Mus; Neurons; Optics; Pathway interactions; Penetration; Physiological; Physiology; Preparation; Primates; Process; Reporter; Reporting; Resolution; Retina; Retinal; Retinal Ganglion Cells; Rodent; Role; Staging; Stimulus; Technology; Testing; Viral; Virus; Vision; Visual; adaptive optics; base; calcium indicator; cell type; cellular imaging; cellular transduction; density; ganglion cell; improved; in vivo; information processing; mouse model; new technology; novel; novel strategies; research study; response; retrograde transport; transduction efficiency; visual information

DESCRIPTION (provided by applicant): The primate retina contains more than 17 classes of ganglion cells, but the contribution to vision of all but a few of these classes is unknown. This large gap in understanding is due to the fact that most ganglion cell types form such sparse mosaics that it is difficult with a single microelectrode or even an array of microelectrodes to record from enough cells of any given class to characterize its functional role. Another limitation of microelectrode technology is that the recording process is invasive, requiring penetration of the globe or, in the case of an eyecup preparation, enucleation of the eye. This precludes the ability to repeat experiments on the same cells and limits behavioral experiments on the same animals in which electrical responses have been obtained. However, rapid advances are being made in the development of reporter molecules that allow optical monitoring of the electrical responses of single neurons with multiphoton fluorescence. Moreover, the recent development of adaptive optics for correcting the eye's aberrations now makes it possible to image individual ganglion cells at ~ 2 micron resolution in the living primate eye. We will develop a new technology for retinal physiology, Functional Adaptive-optics Cellular Imaging in the Living Eye (FACILE) that combines adaptive optics in vivo imaging with optical recording to map the electrical activity of each of the several hundred ganglion cells simultaneously in a patch of monkey retina. We will use viral transduction to insert a genetically encoded calcium indicator (GCaMP3) into ganglion cells, exploring two delivery methods to further improve viral transduction of macaque ganglion cells: intravitreal injection of adeno- associated virus (AAV) in collaboration with John Flannery at UC, Berkeley and retrograde transport of pseudotyped equine anemia immunodeficiency virus (EAIV) injected into retino-recipient nuclei in collaboration with Ed Callaway at the Salk Institute. The development of FACILE will accelerate the complete characterization of the many pathways from the retina to the brain and will reveal the full contribution the retina makes to visual information processing. We will undertake early development of FACILE in a mouse model, and deploy the mature technology in monkey retina. In years 4-5, we will demonstrate the value of the approach by resolving the long-standing debate about whether the macaque retina contains direction-selective neurons, such as those that have been identified in the retinas of several other mammals. PUBLIC HEALTH RELEVANCE: The primate retina contains more than 17 classes of ganglion cells, but the contribution to vision of all but a few of these classes is unknown, a consequence of the weakness of existing physiological methodology for understanding novel cell types. This project will develop a new technology for retinal physiology, Functional Adaptive-optics Cellular Imaging in the Living Eye (FACILE) that combines adaptive optics in-vivo imaging with optical recording to map the electrical activity of each of the several hundred ganglion cells simultaneously in a patch of monkey retina. The novel approach will be used to examine the possibility that among the unknown ganglion cell classes are directionally selective ganglion cells, as in other mammalian retinas. This methodology will accelerate our analysis of the full contribution of the many pathways from retina to brain in primate visual information processing.

描述(申请人提供)：灵长类动物的视网膜包含超过17类神经节细胞，但除了少数几类细胞外，所有这些细胞对视觉的贡献尚不清楚。这种认识上的巨大差距是由于大多数神经节细胞类型形成了如此稀疏的嵌合体，以至于使用单个微电极甚至微电极阵列很难从任何给定类别的足够多的细胞中记录来表征其功能作用。微电极技术的另一个限制是记录过程是侵入性的，需要穿透眼球，或者在眼罩准备的情况下，需要摘除眼睛。这排除了在相同细胞上重复实验的能力，并限制了在获得电反应的相同动物上进行行为实验。然而，报告分子的开发正在迅速取得进展，这种分子可以用多光子荧光对单个神经元的电反应进行光学监测。此外，最近用于矫正眼睛像差的自适应光学的发展使在活的灵长类动物的眼睛中以~2微米的分辨率成像单个神经节细胞成为可能。我们将开发一种用于视网膜生理学的新技术--功能自适应光学活眼细胞成像(Facile)，它将自适应光学体内成像与光学记录相结合，以同时绘制猴子视网膜斑块中数百个神经节细胞的电活动图。我们将使用病毒转导将基因编码的钙指示剂(GCaMP3)插入神经节细胞，探索两种进一步提高猕猴神经节细胞病毒转导的输送方法：与加州大学伯克利分校的John Flannery合作，在玻璃体内注射腺相关病毒(AAV)；与Salk Institute的Ed Callaway合作，将假型马贫血免疫缺陷病毒(EAIV)逆行注射到视网膜受体核中。FILILE的发展将加速从视网膜到大脑的许多通路的完整表征，并将揭示视网膜对视觉信息处理的全部贡献。我们将在小鼠模型上进行早期开发，并将成熟的技术部署在猴子的视网膜上。在第4-第5年，我们将通过解决有关猕猴视网膜是否包含方向选择神经元的长期争论来证明该方法的价值，例如在其他几种哺乳动物的视网膜中发现的那些神经元。 与公共健康相关：灵长类视网膜包含超过17类神经节细胞，但除了少数几类细胞外，所有这些细胞对视觉的贡献尚不清楚，这是由于现有生理学方法在理解新细胞类型方面的薄弱。该项目将开发一种用于视网膜生理学的新技术--功能自适应光学活眼细胞成像(Facile)，它将自适应光学体内成像与光学记录相结合，以同时绘制猴子视网膜斑块中数百个神经节细胞的电活动图。这种新的方法将被用来研究在未知的神经节细胞类别中是否存在方向选择性的神经节细胞，就像在其他哺乳动物的视网膜中一样。这一方法论将加速我们分析从视网膜到大脑的许多通路在灵长类视觉信息处理中的全部贡献。