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Complex genetic encoding of experience by NPAS4 resulting in a sophisticated reorganization of inhibition.

NPAS4 对经验进行复杂的遗传编码，导致复杂的抑制重组。

基本信息

批准号：
10335151
负责人：
Daniel A Heinz
金额：
$ 4.31万
依托单位：
UNIVERSITY OF CALIFORNIA, SAN DIEGO
依托单位国家：
美国
项目类别：
财政年份：
2020
资助国家：
美国
起止时间：
2020-12-01 至 2023-11-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10335151
关键词：
Action Potentials Binding Biology Brain Calcium Channel Cell physiology Cells Cholecystokinin Complex Dendrites Environment Etiology Exposure to FRAP1 gene Fire - disasters Gene Expression Gene Expression Regulation Genetic Genetic Identity Genetic Transcription Genome Hippocampus (Brain)Human Inhibitory Synapse Interneurons Lead Link Location Mediating Messenger RNA Molecular Mus Myoepithelial cell NPAS4 gene Nervous System Physiology Neurologic Dysfunctions Neuronal Plasticity Neurons Organizational Change Pathway interactions Pattern Play Process Regulation Role Slice Source Synapses Synaptic Potentials Testing Transcript Translations Work cell type design environmental enrichment for laboratory animals experience experimental study hippocampal pyramidal neuron insight nervous system disorder neuronal cell body neuronal circuitry novel optogenetics programs relating to nervous system response transcription factor voltage voltage clamp

项目摘要

Project Abstract When a mouse explores an enriched environment the pyramidal neurons in the CA1 region of its hippocampus receive excitatory inputs and fire action potentials to encode information about their complex environment. This experience-induced activity results in the expression of the activity dependent transcription factor NPAS4 via de novo transcription and translation, as well as local dendritic translation of preexisting NPAS4 mRNA. This enriched environment induced NPAS4 produces changes in gene expression resulting in a sophisticated reorganization of inhibition across the somato-dendritic axis, with an increase in the number CCK Basket Cell synapses onto the somatic region and a decrease in the number of inhibitory synapses on the radiatum dendrites of NPAS4 expressing cells. This proposal describes experiments designed to determine 1) the genetic identity of the radiatum targeting interneuron type which loses synapses onto NPAS4 expressing cells, and 2) the necessity of dendritic translation of NPAS4 in this sophisticated reorganization. These experiments will provide insight into fundamental biology underlying the complex regulation of inhibitory networks and the role that experience and activity dependent dendritic translation play in this process. Given the known relationships between dysregulation of inhibition, dendritic translation, and a variety of neurological disorders with experience dependent symptomology, this work will aid our understanding of neurological function and dysfunction.

项目摘要当小鼠探索丰富的环境时，其海马区CA1区的锥体神经元接收兴奋性输入和激发动作电位，以编码有关其复杂环境的信息。这经验诱导的活性导致活性依赖的转录因子NPAS4通过De Novo转录和翻译，以及先前存在的NPAS4 mRNA的局部树突翻译。这丰富的环境诱导NPAS4产生基因表达的变化，导致复杂的横跨躯体-树突轴的抑制重组，CCK篮子细胞数量增加体细胞区的突触和放射状树突上抑制性突触的数量减少表达NPAS4的细胞。这份提案描述了用来确定1)基因同一性的实验与NPAS4表达细胞失去突触的辐射靶向中间神经元型，以及2) 在这种复杂的重组中，NPAS4的树状结构翻译是必要的。这些实验将提供洞察抑制网络复杂调控的基础生物学及其作用依赖于经验和活动的树突翻译在这一过程中发挥了作用。考虑到已知的关系抑制失调、树突状细胞转化和各种神经功能障碍之间的关系依赖症状学，这项工作将有助于我们了解神经功能和功能障碍。