Mechanisms and Functions of Presynaptic Plasticity

突触前可塑性的机制和功能

• 批准号: 7619338
• 负责人: Craig C Garner
• 金额: $ 8.85万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-09-05 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7619338
• 关键词: Behavior; Biochemical Genetics; Brain; Cerebellum; Cyclic AMP; Goals; Image; Individual; Learning; Long-Term Potentiation; Mediating; Memory; Modification; Molecular; Mus; N-Methyl-D-Aspartate Receptors; Physiological; Property; Protein Isoforms; Proteins; Role; Structure; Synapses; Synaptic plasticity; Thinking; experience; genetic analysis; interest; neural circuit; neurotransmitter release; presynaptic; programs; response

DESCRIPTION (provided by applicant): Long-lasting neural circuit modifications are thought to underlie all forms of adaptive and pathological experience-dependent plasticity. Thus there has been great interest in elucidating the mechanisms and functions of various forms of synaptic plasticity. While historically NMDA receptor-dependent long-term potentiation (LTP) has been the prototypic and most extensively studied form of long-lasting synaptic plasticity, it is clear that several key circuits in the mammalian brain express an NMDA receptor-independent form of LTP that is triggered by increases in cAMP and mediated by a long-lasting enhancement of neurotransmitter release. The central goal of this program project is to elucidate the molecular mechanisms and functions of this presynaptic form of LTP. This will be accomplished by analyzing the functional properties of the presynaptic active zone protein RIM to both presynaptic forms of plasticity as well as its contribution to learning and memory in the cerebellum. We have assembled four projects to accomplish these goals. In project #1, we propose a biochemical and genetic analysis of RIM to elucidate the contributions that individual RIM isoforms and domains make to RIM function. In project #2, we will utilize electrophysiological approaches to assess the physiological functions of RIM isoforms and discrete RIM domains to different forms of presynaptic plasticity. In project #3, we propose a set of cellular and dynamic imaging studies to examine how RIM proteins regulate the dynamics of key active zone proteins in response to synaptic activity. Finally, in project #4, we proposed to integrate these RIM structure function studies to assess the role that presynaptic forms of plasticity contribute to VOR plasticity in the mouse cerebellum. These studies will advance our understanding of not only how RIM proteins regulate neurotransmitter release, but also how presynaptic forms of long-lasting plasticity contribute to both neural circuit behavior and experience dependent plasticity.

描述（由申请人提供）：长期的神经回路改变被认为是所有形式的适应性和病理性经验依赖可塑性的基础。因此，阐明各种形式的突触可塑性的机制和功能已引起人们极大的兴趣。虽然历史上NMDA受体依赖的长期增强（LTP）一直是持久突触可塑性的原型和最广泛研究的形式，但很明显，哺乳动物大脑中的几个关键回路表达NMDA受体独立形式的LTP，该LTP由cAMP的增加触发，并由神经递质释放的长期增强介导。本项目的中心目标是阐明LTP突触前形式的分子机制和功能。这将通过分析突触前活性区蛋白RIM对突触前可塑性形式及其对小脑学习和记忆的贡献的功能特性来完成。我们已经制定了四个项目来实现这些目标。在项目#1中，我们提出了RIM的生化和遗传分析，以阐明单个RIM异构体和结构域对RIM功能的贡献。在项目#2中，我们将利用电生理学方法来评估RIM同工异构体和离散RIM结构域对不同形式的突触前可塑性的生理功能。在项目#3中，我们提出了一套细胞和动态成像研究，以检查RIM蛋白如何调节关键活性区蛋白的动态以响应突触活动。最后，在项目#4中，我们建议整合这些RIM结构功能研究，以评估突触前形式的可塑性对小鼠小脑VOR可塑性的作用。这些研究将促进我们对RIM蛋白如何调节神经递质释放的理解，以及突触前形式的持久可塑性如何促进神经回路行为和经验依赖的可塑性。