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MOLECULAR AND GENETIC ANALYSIS OF GPR126 IN PERIPHERAL NERVE.

周围神经中 GPR126 的分子和遗传分析。

基本信息

批准号：
8806057
负责人：
Kelly R Monk
金额：
$ 3.53万
依托单位：
WASHINGTON UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-05-01 至 2016-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8806057
关键词：
Address Adhesions Adult Axon Biochemical Cell Adhesion Molecules Cell Culture Techniques Cell Differentiation process Cell Proliferation Cell-Matrix Junction Cells Complement Factor B Cyclic AMP Cyclic AMP Receptors Cyclic AMP-Responsive DNA-Binding Protein Data Demyelinations Development Disease Drug Targeting Embryo Ensure Foundations Future G Protein-Coupled Receptor Signaling G-Protein-Coupled Receptors Gap Junctions Genetic Transcription Goals Heterotrimeric GTP-Binding Proteins Homeostasis Human In Vitro Injury Knockout Mice Lead Learning Ligands Maintenance Mammals Membrane Molecular Molecular Analysis Morbidity - disease rate Multiple Sclerosis Mus Mutant Strains Mice Myelin Myelin Sheath Natural regeneration Nerve Nervous System Physiology Nervous system structure Neurons Nuclear Paralysed Pathway interactions Patients Perinatal Peripheral Nerves Peripheral Nervous System Peripheral Nervous System Diseases Pharmaceutical Preparations Phenotype Protein Kinase Proteins Recovery Reporting Role Schwann Cells Seminal Signal Pathway Signal Transduction Spinal cord injury Staging Symptoms Testing Therapeutic Time Tissues Transgenic Mice Transmembrane Domain Travel Work Zebrafish base cell type extracellular falls fascinate genetic analysis human GPRC5C protein in vivo injured mutant myelination nerve injury nervous system development nervous system disorder neuron loss prevent receptor remyelination repaired research study small molecule therapeutic target therapy development

项目摘要

DESCRIPTION (provided by applicant): Myelin is a layer of insulation that covers neuronal projections called axons in the vertebrate nervous system. In the peripheral nervous system, specialized cells called Schwann cells spiral themselves around axons to form the myelin sheath. Myelin ensures that nerve impulses travel quickly and efficiently, ultimately allowing for the entire nervous system to function properly. Disruptions to the myelin sheath in disease (like multiple sclerosis or peripheral neuropathy) or after injury (like spinal cord trauma) lead to devastating symptoms, significant morbidity, and myelin loss can lead to permanent neuron loss, and ultimately, paralysis. Currently, no treatments exist to prevent demyelination or to hasten remyelination, and there is therefore a pressing need to develop therapies that address these issues. To this end, we must learn more about the mechanisms that govern myelination, myelin maintenance, and remyelination. We discovered that the orphan G protein-coupled receptor, Gpr126, is an essential component of the incompletely understood axon-Schwann cell signaling nexus that controls myelination. In Gpr126 mutant mice, Schwann cells associate with axons, but fail to spiral their membranes to generate the myelin sheath. G protein-coupled receptors are excellent drug targets, representing at least one-third of all approved drugs; thus, Gpr126 represents an extremely attractive potential target to stimulate remyelination in humans with myelin disease or injury. We therefore propose to dissect the mechanisms by which Gpr126 controls myelination and to determine if Gpr126 is required for myelin homeostasis or remyelination after injury. These studies encompass our broad goals to define the mechanisms that form, maintain, and regenerate myelinated axons in the vertebrate nervous system. In the first aim, we will define the signaling pathway downstream of Gpr126 activation by performing biochemical analyses on Gpr126 mutant tissue and cells. In the second aim, we will test the hypothesis that Gpr126 is required autonomously in Schwann cells for myelination. We will employ conditional mouse mutants to delete Gpr126 specifically in Schwann cells or in neurons, and we will perform immunohistochemical and ultrastructural analyses to determine the consequences of cell type specific loss. In this aim, we will also define the developmental window of Gpr126 requirement by temporally deleting Gpr126 in developing embryonic and perinatal transgenic mice. In the third aim, we will define the roles of Gpr126 in adult peripheral nerve. Specifically, we will determine if Gpr126 is required for myelin maintenance, demyelination, and/or remyelination after nerve injury by temporally deleting Gpr126 in mature nerve and in injured mature nerve. Together, these experiments will define the mechanisms by which Gpr126 controls myelination, will elucidate if Gpr126 is required for remyelination in adult nerve, and may lay the foundation for future therapeutics that stimulate myelin repair in humans.

描述（由申请人提供）：髓磷脂是一层绝缘层，覆盖在脊椎动物神经系统中称为轴突的神经元突起。在周围神经系统中，被称为雪旺细胞的特化细胞在轴突周围旋转，形成髓鞘。髓磷脂确保神经冲动快速有效地传递，最终使整个神经系统正常运作。髓鞘在疾病（如多发性硬化症或周围神经病变）或损伤（如脊髓损伤）后受到破坏会导致毁灭性的症状，严重的发病率，髓鞘丢失会导致永久性神经元丢失，最终导致瘫痪。目前，没有任何治疗方法可以防止脱髓鞘或加速脱髓鞘再生，因此迫切需要开发治疗方法来解决这些问题。为此，我们必须更多地了解髓鞘形成、髓磷脂维持和再髓鞘形成的机制。我们发现孤儿G蛋白偶联受体Gpr126是控制髓鞘形成的不完全了解的轴突-雪旺细胞信号通路的重要组成部分。在Gpr126突变小鼠中，雪旺细胞与轴突结合，但不能螺旋膜产生髓鞘。G蛋白偶联受体是极好的药物靶点，占所有批准药物的至少三分之一；因此，Gpr126是刺激髓鞘疾病或损伤患者髓鞘再生的极具吸引力的潜在靶点。因此，我们建议剖析Gpr126控制髓鞘形成的机制，并确定Gpr126是否需要髓鞘稳态或损伤后的再髓鞘形成。这些研究涵盖了我们的广泛目标，即确定脊椎动物神经系统中髓鞘轴突形成、维持和再生的机制。在第一个目标中，我们将通过对Gpr126突变组织和细胞进行生化分析来确定Gpr126激活的下游信号通路。在第二个目标中，我们将测试假设Gpr126是雪旺细胞中髓鞘形成自主需要的。我们将使用条件小鼠突变体在雪旺细胞或神经元中特异性地删除Gpr126，我们将进行免疫组织化学和超微结构分析，以确定细胞类型特异性丢失的后果。为此，我们还将通过在发育中的胚胎和围产期转基因小鼠中暂时删除Gpr126来确定Gpr126需求的发育窗口。在第三个目标中，我们将定义Gpr126在成人外周中的作用