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In Vivo Analysis of the Developing Vertebrate Retina

In Vivo Analysis of the Developing Vertebrate Retina
脊椎动物视网膜发育的体内分析
批准号:
6696894
负责人:
Rachel O Wong
金额:
$26.78万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-02-01 至 2008-01-31

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中文摘要
翻译
描述(由申请人提供):神经系统中的突触连接具有高度特异性。在中枢神经系统的某些区域,突触特异性来自于更分散的早期连接模式的重组,而在其他区域,精确的模式可能从一开始就存在。因此,神经生物学中最具挑战性和最重要的问题之一是如何在发育过程中精确地建立神经回路。我们有兴趣了解神经回路是如何形成和组织在脊椎动物视网膜,特别是如何潜在的前和突触后细胞之间的相互作用,指导这一过程中的发展。虽然已经从体外工作中获得了很多知识,但很明显,在体内检查这一过程将提供对建立突触特异性所发生的动态相互作用的深入了解。斑马鱼是研究视网膜回路在体发育的理想模型。这是因为突触形成在受精后几天内完成,并且斑马鱼胚胎可以保持透明,使其适合在突触形成和成熟期间进行体内成像。在本申请中,我们建议专注于内层视网膜中网络的发展。我们将确定视网膜神经节细胞的突触后树突和无长突细胞的突触前末梢的生长和发育,它们共同形成第一个视网膜网络,在发育过程中接触并形成突触区域,即内丛状层(IPL)。我们将结合联合收割机的时间推移在体内成像技术与分子的方法来阐明IPL发展的正常模式,然后应用这些技术与使用视网膜突变体,以确定组织这个突触层的细胞-细胞相互作用的作用。总之,拟议的研究结果将进一步加深我们对内部视网膜回路的结构和功能发育机制的理解。
英文摘要
DESCRIPTION (provided by applicant): Synaptic connections in the nervous system are highly specific. In some regions of the central nervous system, synapse specificity arises from the reorganization of more diffuse, early patterns of connectivity whereas in other regions, precise patterns may be present from the very beginning. Thus, one of the most challenging and important issues in neurobiology concerns how neuronal circuits are established with precision during development. We are interested in understanding how neural circuits are formed and organized in the vertebrate retina, and in particular how interactions between potential pre- and postsynaptic cells guide this process during development. Although much knowledge has been gained from in vitro work, it is evident that examining this process in vivo will provide insight into the dynamic interactions that take place to establish synaptic specificity. The zebrafish is an ideal model for studying the in vivo development of retinal circuits. This is because synapse formation is completed within a few days after fertilization and the zebrafish embryo can be maintained transparent, making it suitable for in vivo imaging throughout the period of synapse formation and maturation. In this application, we propose to focus on the development of networks in the inner retina. We will determine how outgrowth and elaboration of the postsynaptic dendrites of retinal ganglion cells and the presynaptic terminals of amacrine cells, that together form the first retinal network, contact and form the synaptic region, the inner plexiform layer (IPL) during development. We will combine time-lapse in vivo imaging techniques with molecular approaches to elucidate the normal pattern of IPL development, and then apply these techniques together with the use of retinal mutants to ascertain the role of cell-cell interactions in organizing this synaptic layer. Together, the results of the proposed studies will further our understanding of the mechanisms underlying the structural and functional development of the inner retinal circuitry.
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Retinal foveal midget connectivity after acute photoreceptor loss
  • 批准号:
    10350118
  • 项目类别:
  • 资助金额:
    $19.44万
  • 财政年份:
    2022
  • 负责人:
    Rachel O Wong
  • 依托单位:
Retinal foveal midget connectivity after acute photoreceptor loss
  • 批准号:
    10541889
  • 项目类别:
  • 资助金额:
    $23.33万
  • 财政年份:
    2022
  • 负责人:
    Rachel O Wong
  • 依托单位:
Circuit Assembly in the Vertebrate Retina-Supplement
  • 批准号:
    8792319
  • 项目类别:
  • 资助金额:
    $2.11万
  • 财政年份:
    2014
  • 负责人:
    Rachel O Wong
  • 依托单位:
2013 Dendrites: Molecules, Structure and Function Gordon Research Conference and
  • 批准号:
    8527252
  • 项目类别:
  • 资助金额:
    $2.3万
  • 财政年份:
    2013
  • 负责人:
    Rachel O Wong
  • 依托单位:
国内基金
海外基金
RNA干扰大鼠NgR蛋白及其对脊髓损伤的修复作用
C.elegans unc突变不育表型相关基因的鉴定及其功能研究
  • 批准号:
    30470937
  • 项目类别:
    面上项目
  • 资助金额:
    25.0万元
  • 批准年份:
    2004
  • 负责人:
    樊启昶
  • 依托单位: