Activity Dependent Control of Visual System Development

视觉系统开发的活动相关控制

• 批准号: 8518326
• 负责人: HOLLIS T. CLINE
• 金额: $ 52.94万
• 依托单位: SCRIPPS RESEARCH INSTITUTE, THE
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-30 至 2014-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8518326
• 关键词: Address; Affect; Animals; Autistic Disorder; Axon; Behavior; Behavioral; Biological Assay; Brain; Cells; DNA Sequence Rearrangement; Data; Dendrites; Development; Electron Microscopy; Ensure; Equilibrium; Evaluation; Excitatory Synapse; Gene Transfer; Genes; Glutamates; Image; Individual; Inhibitory Synapse; Mental Depression; Neurons; Ocular Dominance; Optics; Pattern; Peptides; Photons; Play; Property; Proteins; Resolution; Role; Schizophrenia; Sensory; Site; Synapses; Synaptic Transmission; System; Tadpoles; Technology; Tectum Mesencephali; Testing; Time; Visual; Visual system structure; Xenopus; avoidance behavior; cellular imaging; critical period; experience; in vivo; inhibitory neuron; interest; nervous system disorder; neuron development; prevent; promoter; public health relevance; research study; response; retinotectal; superior colliculus Corpora quadrigemina; synaptogenesis; tool; transmission process; vision development; visual information; visual receptive field

DESCRIPTION (provided by applicant): GABAergic inhibition is essential for circuit development and function. In the developing visual system, GABAergic inhibition determines the onset and close of the critical period for ocular dominance plasticity. Furthermore, the development of GABAergic synaptic transmission is regulated by visual experience. These studies suggest that sensory input activity regulates the development of GABAergic neurons and their synaptic connections, and that, in turn, inhibitory GABAergic synaptic transmission regulates the development and plasticity of visual circuits. Despite this postulated pivotal role for inhibition in circuit development, the inability to visualize and perturb connectivity of GABAergic inhibitory neurons in an intact developing circuit has prevented a critical evaluation of this hypothesis. We have developed tools to address both of these limitations and now propose experiments to determine mechanisms controlling the development of GABAergic neurons and their synaptic connections in the intact Xenopus tadpole optic tectum and to determine how GABAergic inputs control the development of visual receptive fields and visually guided behavior. To visualize GABAergic neurons in the intact animal, we will use the VGAT promoter to drive expression of fluorescent proteins (FPs) and other genes of interest specifically in GABAergic neurons. We will decrease synaptic transmission onto GABAergic neurons by VGAT-driven expression of peptides which we have shown specifically inhibit GABAergic or glutamatergic synaptic transmission in a cell autonomous manner. In Aim 1, we will collect time-lapse images of individual GABAergic tectal neurons expressing FP and FP-tagged synaptic proteins to identify mechanisms that control GABAergic neuronal development. We will test the role of glutamatergic and GABAergic synaptic transmission in GABAergic neuron development by expressing peptides to block synaptic transmission onto the imaged cell. In Aim 2, we will combine in vivo time-lapse imaging, to identify stable and dynamic dendrites, and retrospective serial section electron microscopy (EM) to determine the synaptic rearrangements that occur during GABAergic neuronal development. Data from Aims 1 and 2 will demonstrate the activity-dependent mechanisms that control the morphological development and synaptic connectivity of GABAergic neurons in vivo. In Aims 3 and 4 we will test the effect of blocking inhibitory and excitatory transmission on tectal visual receptive field properties, using cell-attached and whole recordings, and a visual avoidance assay, that will extend our studies into the behavioral arena. The aberrant development and function of inhibitory circuits is thought to underlie a variety of developmental neurological disorders, including autism, schizophrenia and depression, however the basic mechanisms governing the development of inhibitory circuits are relatively unknown. The experiments proposed here should illuminate activity-dependent mechanisms of GABAergic circuit development in vivo.

描述（由申请人提供）：GABA能抑制对回路发育和功能至关重要。在发育中的视觉系统中，GABA能抑制决定了眼优势可塑性关键期的开始和结束。此外，GABA能突触传递的发展受到视觉经验的调节。这些研究表明，感觉输入活动调节GABA能神经元及其突触连接的发育，反过来，抑制性GABA能突触传递调节视觉回路的发育和可塑性。尽管这种假设的关键作用，抑制电路的发展，无法可视化和干扰连接的GABA能抑制神经元在一个完整的发展电路，阻止了这一假设的关键评价。我们已经开发了工具，以解决这些限制，现在提出的实验，以确定机制控制的GABA能神经元的发展和他们的突触连接在完整的非洲爪蟾蝌蚪视顶盖，并确定如何GABA能输入控制视觉感受野和视觉引导行为的发展。 为了使完整动物中的GABA能神经元可视化，我们将使用VGAT启动子来驱动荧光蛋白（FP）和其他感兴趣的基因在GABA能神经元中的特异性表达。我们将通过VGAT驱动的肽的表达来减少GABA能神经元上的突触传递，我们已经证明所述肽以细胞自主方式特异性抑制GABA能或谷氨酸能突触传递。在目标1中，我们将收集表达FP和FP标记的突触蛋白的单个GABA能顶盖神经元的延时图像，以确定控制GABA能神经元发育的机制。我们将通过表达肽来阻断突触传递到成像细胞上，来测试多巴胺能和GABA能突触传递在GABA能神经元发育中的作用。在目标2中，我们将结合联合收割机在体内的时间推移成像，以确定稳定和动态树突，并回顾性连续切片电子显微镜（EM），以确定突触重排发生在GABA能神经元的发育。来自目标1和2的数据将证明控制体内GABA能神经元的形态发育和突触连接的活性依赖性机制。在目标3和4中，我们将测试阻断抑制性和兴奋性传递对顶盖视觉感受野特性的影响，使用细胞附着和整体记录，以及视觉回避测定，这将把我们的研究扩展到行为竞技场。抑制回路的异常发育和功能被认为是各种发育性神经障碍的基础，包括自闭症、精神分裂症和抑郁症，然而控制抑制回路发育的基本机制相对未知。这里提出的实验应阐明活性依赖的机制，GABA能电路的发展在体内。