Amacrine Cell Function in the Retina

视网膜无长突细胞功能

• 批准号: 8238345
• 负责人: Stewart Allen Bloomfield
• 金额: $ 55.27万
• 依托单位: NEW YORK UNIVERSITY SCHOOL OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 1988
• 资助国家: 美国
• 起止时间: 1988-03-01 至 2013-01-06
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8238345
• 关键词: Acetylcholine; Affect; Amacrine Cells; Applications Grants; Architecture; Area; Axon; Biological Assay; Brain; Cell physiology; Cells; Cellular Morphology; Charcot-Marie-Tooth Disease; Circadian Rhythms; Code; Communication; Computer Simulation; Conflict (Psychology); Connexins; Coupled; Coupling; Data; Data Collection; Defect; Dendrites; Dopamine; Dyes; Economics; Feedback; GABA Receptor; Gap Junctions; Generations; Goals; Grant; Health; Human; Individual; Inner Nuclear Layer; Intercellular Junctions; Investigation; Knock-out; Knockout Mice; Label; Laboratories; Light; Light Adaptations; Lighting; Link; Masks; Mediating; Methodology; Modality; Motion; Movement; Mus; Mutant Strains Mice; Neurobiology; Neurologic; Neuromodulator; Neurons; Nicotinic Agonists; Nitric Oxide; Oryctolagus cuniculus; Output; Pathway interactions; Pattern; Physiological; Picrotoxin; Play; Preparation; Presynaptic Terminals; Property; Proteins; Regulation; Research; Response to stimulus physiology; Retina; Retinal; Retinal Cone; Retinal Diseases; Role; Shaw potassium channel protein family; Shunt Device; Signal Transduction; Somatic Cell; Speed; Stimulus; Stress; Stroke; Structure; Structure-Activity Relationship; Synapses; Synaptic Transmission; Techniques; Testing; Time; Tracer; Translating; Translations; Trauma; Vertebrate Photoreceptors; Vision; Visual; Whole-Cell Recordings; Work; base; cholinergic; cohort; connexin 36; deafness; experience; extracellular; gamma-Aminobutyric Acid; ganglion cell; genetic manipulation; horizontal cell; insight; mutant mouse model; nerve supply; nervous system disorder; neurobiotin; neuronal cell body; neuroprotection; postsynaptic; preference; prevent; research study; response; retinal neuron; retinal rods; stem; synaptic function; transmission process; visual process; visual processing; voltage

DESCRIPTION (provided by applicant): Work over the last decade indicates that electrical synaptic transmission via gap junctions forms an important mode of neuronal communication in the retina. It is now clear that gap junctions are ubiquitous in the retina, being expressed by each of the five major cell classes. In addition, retinal gap junctions have been shown to be dynamically regulated by changes in ambient illumination and circadian rhythms acting through light-activated neuromodulators such as dopamine and nitric oxide. These data suggest that gap junctions play an important role in light adaptation. The long-term goal of our research is define the distribution and function of gap junctions in the mammalian retina so as to define their roles in the processing of visual signals. One specific aim of this proposal is to examine the role of gap junctions in the transmission of rod-mediated signals. Experiments are proposed to study the role of coupling between AII amacrine cells in maintaining the fidelity of the most sensitive rod signals and the role of rod-cone coupling in delivering rod-mediated signals to the horizontal cells. A second aim is to study masked synaptic inputs to retinal neurons, delivered by circuits that utilize gap junctions. Our recent data indicate that rod-mediated synaptic signals to some ganglion cell subtypes are masked in that they are not translated into a spike code and sent to the brain. A second masked input that will be studied is an OFF response in ON direction selective ganglion cells that is delivered by gap junctions made with a subtype of polyaxonal amacrine cells and is normally hidden by inhibitory circuitry. We will determine if masked synaptic inputs in the retina reflect normal dynamics in visual signaling with changing stimulus conditions or a strategy for economic wiring of the retina. A third aim is to study the role of starburst amacrine cell Kv3 potassium channels in generating direction selective responses, a computation whose mechanism has become a classic question in retinal neurobiology. A final aim is to define the structure and function of the 20-30 subtypes of amacrine cells in the mammalian retina to elucidate their roles in generating the output signals of the retina carried by the postsynaptic ganglion cells to the brain. The proposed experiments center on electrophysiological recording of the responses of retinal neurons and their labeling with the gap-permeant biotinylated tracers. The function of gap junctions will be assessed by selectively ablating them either pharmacologically or by knocking out specific connexin proteins in mutant mouse models. Gap junctions have been implicated in a number of neurological diseases including X- linked Charcot-Marie-Tooth disease, nonsyndromic autosomal deafness and neuroprotection following stroke or trauma. Although focused on the function and regulation of gap junctions in mammalian retina, the proposed work will nevertheless provide important insights into the roles of electrical synaptic transmission throughout the brain. PUBLIC HEALTH RELEVANCE: As the most important sense in humans, vision is the modality through which we interact mainly with the world around us. This proposal will examine the role of gap junctions in the retina, which are modulated by light and are thereby likely to play a key role in light adaptation. Gap junctions have been implicated in a number of neurological defects including X-linked Charcot-Marie-Tooth disease, nonsyndromic autosomal deafness and neuroprotection and may play a role in retinopathies related to adaptation and vision under dim ambient light conditions.

描述（由申请人提供）：过去十年的工作表明，经由间隙连接的电突触传递形成视网膜中神经元通信的重要模式。现在很清楚，缝隙连接在视网膜中无处不在，由五种主要细胞类别中的每一种表达。此外，视网膜缝隙连接已被证明是动态调节的环境照明和昼夜节律的变化，通过光激活的神经调节剂，如多巴胺和一氧化氮的作用。这些数据表明缝隙连接在光适应中起着重要作用。本研究的长期目标是明确缝隙连接在哺乳动物视网膜中的分布和功能，从而明确其在视觉信号处理中的作用。这个建议的一个具体目的是研究间隙连接在杆介导的信号传递中的作用。实验提出研究AII无长突细胞之间的耦合在保持最敏感的杆信号的保真度和杆锥耦合在传递杆介导的信号的水平细胞的作用。第二个目标是研究视网膜神经元的掩蔽突触输入，由利用缝隙连接的电路传递。我们最近的数据表明，一些神经节细胞亚型的视杆介导的突触信号被掩盖，因为它们没有被翻译成尖峰代码并发送到大脑。将被研究的第二个掩蔽输入是ON方向选择性神经节细胞的OFF响应，其由用多轴突无长突细胞亚型制成的间隙连接递送，并且通常被抑制性电路隐藏。我们将确定视网膜中的掩蔽突触输入是否反映了随着刺激条件的变化或视网膜经济布线策略的视觉信号的正常动态。第三个目的是研究星爆无长突细胞Kv 3钾通道在产生方向选择性反应中的作用，该计算的机制已成为视网膜神经生物学中的经典问题。最后的目的是确定哺乳动物视网膜中20-30种无长突细胞亚型的结构和功能，以阐明它们在产生由突触后神经节细胞携带到大脑的视网膜输出信号中的作用。本实验主要研究视网膜神经元的电生理记录及其生物素标记。间隙连接的功能将通过在突变小鼠模型中选择性地消融它们或通过敲除特定的连接蛋白来评估。缝隙连接与许多神经系统疾病有关，包括X连锁腓骨肌萎缩症、非综合征性常染色体耳聋和中风或创伤后的神经保护。虽然专注于哺乳动物视网膜缝隙连接的功能和调节，但拟议的工作将为整个大脑的电突触传递的作用提供重要的见解。作为人类最重要的感官，视觉是我们与周围世界互动的主要方式。该建议将研究视网膜中缝隙连接的作用，缝隙连接受光调制，因此可能在光适应中发挥关键作用。缝隙连接与许多神经系统缺陷有关，包括X-连锁Charcot-Marie-Tooth病、非综合征性常染色体耳聋和神经保护，并可能在昏暗环境光条件下与适应和视力相关的视网膜病变中发挥作用。