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Investigating how signaling via adhesion GPCR Latrophilins regulates synapse formation and specificity in the hippocampus

研究通过粘附 GPCR Latrophilins 发出的信号如何调节海马突触的形成和特异性

基本信息

批准号：
10545731
负责人：
Richard Cheslock Sando
金额：
$ 23.96万
依托单位：
VANDERBILT UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2018
资助国家：
美国
起止时间：
2018-07-13 至 2024-01-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10545731
关键词：
Adhesions Affinity Amygdaloid structure Anxiety Arrestins Attention deficit hyperactivity disorder Behavior Behavioral Binding Biological Assay Brain Cadherins Cell Adhesion Molecules Cell Volumes Cells Central Nervous System Complement Coupling Cyclic AMP Data Development EGF gene Electrophysiology (science)Excitatory Synapse Exhibits Fibronectins Future G Protein-Coupled Receptor Signaling G-Protein-Coupled Receptors GPCR Signaling Pathway GTP-Binding Proteins Genetic Polymorphism Genomics Hippocampus Homer 1 Image Imaging Techniques Impairment Invertebrates Lentivirus Leucine-Rich Repeat Ligands Light Link Luciferases Maintenance Measures Mediating Modeling Molecular Morphology Mus Neurons Orphan Pathway interactions Perforant Pathway Phase Physiology Process Property Proteins Pyramidal Cells Reporter Resources Role Second Messenger Systems Signal Pathway Signal Transduction Social Behavior Specific qualifier value Specificity Stereotyping Synapses Testing Time Training Universities Vertebral column Vertebrates Viral Visualization alpha-latrotoxin receptor axonal pathfinding behavioral study biocytin confocal imaging density experimental study extracellular hippocampal pyramidal neuron information processing insight mutant nanobodies nervous system disorder neural circuit neuropsychiatric disorder neuroregulation novel optogenetics phosphoric diester hydrolase postsynaptic presynaptic receptor response social synaptic function synaptogenesis tool ultra high resolution

项目摘要

PROJECT SUMMARY: Brain functions require the assembly and maintenance of distinct synaptic subtypes into stereotyped neural circuits. However, the fundamental cellular and molecular mechanisms underlying input-specific synapse formation in neural circuits remain poorly understood. Our studies during the K99 phase revealed an important role of the adhesion GPCR Latrophilins (Lphns) in hippocampal excitatory synaptic specificity. We recently found using rescue experiments that the role of Lphn2/3 in hippocampal input-specific excitatory synapse formation requires G-protein and/or u-Arrestin coupling. In parallel studies, we found that compartmentalized postsynaptic cAMP signaling is a prominent driver of excitatory synapse formation. Efforts during the R00 phase at Vanderbilt University will be focused on examining the G-protein and u-Arrestin intracellular signaling mechanisms of Lphns and other adhesion GPCRs at synapses in the mammalian central nervous system. Furthermore, we will determine the functions of unstudied adhesion GPCRs in neural circuits, and define the extracellular ligands of orphan adhesion GPCRs in the brain. We will develop novel molecular tools including viral-mediated nanobody targeting of signaling modulators to probe the roles of compartmentalized synaptic signaling pathways in input-specific excitatory, inhibitory and neuromodulatory synapse formation in neural circuits. We will also develop novel live super-resolution STORM and confocal imaging techniques to image synapse formation, maintenance and elimination in real-time. We expect these studies to reveal fundamental principles of how neural circuits are established by diverse synapses in the mammalian central nervous system, and elucidate the functions and signaling mechanisms of the understudied adhesion GPCRs in the brain.

项目概要：大脑功能需要组装和维持不同的突触亚型到定型的神经回路中。然而，神经回路中输入特异性突触形成的基本细胞和分子机制仍然知之甚少。我们在K99期的研究揭示了粘附GPCR Latrophilins（Lphns）在海马兴奋性突触特异性中的重要作用。我们最近发现使用救援实验，Lphn 2/3在海马输入特异性兴奋性突触形成中的作用需要G蛋白和/或u-Arrestin偶联。在平行的研究中，我们发现隔室化的突触后cAMP信号传导是兴奋性突触形成的重要驱动因素。在范德比尔特大学的R 00阶段的努力将集中在研究哺乳动物中枢神经系统突触处Lphns和其他粘附GPCR的G蛋白和u-抑制蛋白细胞内信号传导机制。此外，我们将确定未研究的粘附GPCRs在神经回路中的功能，并确定脑中孤儿粘附GPCRs的细胞外配体。我们将开发新的分子工具，包括病毒介导的靶向信号调节剂的纳米抗体，以探测神经回路中输入特异性兴奋性，抑制性和神经调节性突触形成中的区室化突触信号通路的作用。我们还将开发新的实时超分辨率STORM和共聚焦成像技术，以实时成像突触的形成，维持和消除。我们希望这些研究能够揭示哺乳动物中枢神经系统中不同突触如何建立神经回路的基本原理，并阐明大脑中未充分研究的粘附GPCR的功能和信号转导机制。