Synaptic Adaptation and Plasticity After Chronic Disuse

长期废用后的突触适应和可塑性

• 批准号: 7252659
• 负责人: RICHARD W TSIEN
• 金额: $ 34.24万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-07-16 至 2009-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7252659
• 关键词: Address; Antiepileptic Agents; Axon; Biochemical; Brain; Calcium; Cells; Chromosome Pairing; Chronic; Class; Clinical; Condition; Dendrites; Disease; Disruption; Dissection; Distal; Down Syndrome; Elements; Ensure; Epilepsy; Event; Face; Feedback; Fire - disasters; Fragile X Syndrome; Frequencies; Genetic Transcription; Glutamate Receptor; Goals; Grant; Green Fluorescent Proteins; Health; Hippocampus (Brain); Inborn Genetic Diseases; Individual; Internet; Intervention; Kinetics; Knowledge; Laboratories; Lead; Learning; Link; Measurement; Memory; Modification; Molecular; Mood Disorders; Motion; Neurons; Output; Pathway interactions; Perforant Pathway; Performance; Pharmaceutical Preparations; Physiology; Production; Property; Proteins; Pyramidal Cells; Range; Rate; Regulation; Relative (related person); Signal Pathway; Signal Transduction; Site; Slice; Source; Spinal; Synapses; Synaptic plasticity; System; Testing; Thinking; Translations; Transport Vesicles; Trees; Up-Regulation; Weight; Work; alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid; amino 3 hydroxy 5 methylisoxazole 4 propionate; base; calmodulin-dependent protein kinase II; cognitive function; deprivation; hippocampal pyramidal neuron; millisecond; neuronal cell body; neurotransmission; photoactivation; postsynaptic; presynaptic; relating to nervous system; research study; response; size; trafficking; transmission process

DESCRIPTION (provided by applicant): Synaptic strength must be regulated in the face of changing levels of input in order to ensure that total strength of all inputs are controlled so as to maintain output firing within reasonable limits and these mechanisms must work in conjunction with mechanisms of synaptic plasticity. Its clinical importance can be best illustrated by the condition of epilepsy where these mechanisms are disrupted at the extreme. The association of epilepsy with numerous forms of inherited disorders of cognitive function such as Fragile X and Down Syndrome and the increasing use of anti-epileptic drugs for the treatment of mood disorders highlight the importance of these mechanisms in maintaining normal brain function. This grant proposes to study the underlying mechanisms by which synaptic adaptation is achieved in the face of changing levels of input and the effects of this adaptation on plasticity, building on recent progress in the lab. The first two parts will use strategies to describe more completely the signaling events in the pathway from synaptic input to synaptic modification, taking advantage of the ease of manipulation and measurement in the primary culture system. This part of the study will begin with a careful dissection of the sources of electrical input and calcium entry responsible for the induction of the key signaling events, followed by an elucidation of the mechanisms of regulation of key intermediate signaling products, examining the regulation of their enzymatic activity, stability, transcription, translation and transport to the synapse. In addition, a more complete description of the signaling cascade will be drawn out from microarray studies comparing results from disruption of the signaling pathway at various points. The next part of the study will look closely at the microphysiology of this phenomenon (a) to elucidate the elements of adaptation that are cell-autonomous, by comparing effects of network changes and manipulations in only one cell (b) to describe adaptive changes at the level of single synapses, and (c) to determine the pre- or postsynaptic locus of induction of the various elements of adaptation. These studies will take advantage of long standing expertise in the lab in studying the physiology of single synapses involving focal stimulation and measurement of synaptic responses at unitary sites. The last part of the project will apply the knowledge gained in the previous sections to try to understand the impact of adaptation m intact hippocampal circuits, using the organotypic slice culture. Primary questions addressed will be differences in the expression of adaptation at two different sets of afferents and consequences of this adaptation on the induction and expression of LTP. We will look for forms of LTP not previously found in pyramidal neurons and for changes in the performance of preexisting mechanisms of LTP.

描述（由申请人提供）：突触强度必须在面对输入水平变化时进行调节，以确保所有输入的总强度得到控制，从而将输出激发维持在合理的限度内，并且这些机制必须与突触可塑性机制一起工作。它的临床重要性可以最好地说明了癫痫的条件下，这些机制被破坏的极端。癫痫与许多形式的遗传性认知功能障碍（如脆性X染色体和唐氏综合征）的相关性以及越来越多地使用抗癫痫药物治疗情绪障碍突出了这些机制在维持正常脑功能方面的重要性。这项资助旨在研究突触适应在面对不断变化的输入水平时实现的潜在机制，以及这种适应对可塑性的影响，建立在实验室的最新进展基础上。前两部分将利用原代培养系统中易于操作和测量的优势，使用策略更完整地描述从突触输入到突触修饰的通路中的信号事件。这部分研究将开始，仔细剖析负责诱导关键信号事件的电输入和钙离子进入的来源，然后阐明关键中间信号产物的调节机制，检查其酶活性、稳定性、转录、翻译和转运到突触的调节。此外，一个更完整的描述信号级联将绘制出从微阵列研究比较结果从中断的信号通路在不同的点。本研究的下一部分将密切关注这种现象的微生理学：（a）通过比较网络变化和仅在一个细胞中的操作的影响来阐明细胞自主的适应性要素（B），以描述单个突触水平的适应性变化，以及（c）确定诱导各种适应性要素的突触前或突触后位点。这些研究将利用实验室长期以来的专业知识，研究涉及局灶性刺激和测量单一部位突触反应的单突触生理学。该项目的最后一部分将应用在前几节中获得的知识，试图了解适应完整的海马电路的影响，使用器官型切片培养。主要的问题将是在两个不同的传入和后果的诱导和表达的LTP的适应表达的差异。我们将寻找以前在锥体神经元中未发现的LTP形式，以及LTP先前存在机制的性能变化。