The Role of Microglia in Epilepsy

小胶质细胞在癫痫中的作用

基本信息

批准号：
8764941
负责人：
Long-Jun Wu
金额：
$ 32.48万
依托单位：
RUTGERS, THE STATE UNIV OF N.J.
依托单位国家：
美国
项目类别：
财政年份：
2014
资助国家：
美国
起止时间：
2014-05-01 至 2019-02-28
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8764941
关键词：
Ablation Acute Address Astrocytes Behavior Behavioral Brain Brain Diseases Cells Characteristics Chemotactic Factors Chronic Communication Complement Data Dendrites Dendritic Spines Development Disease Electrophysiology (science)Elements Epilepsy Exhibits Genetic Glutamate Receptor Glutamates Health Hippocampus (Brain)Human Hyperactive behavior Immune Injection of therapeutic agent Kainic Acid Life Mediating Microglia Microscopy Modeling NMDA receptor antagonist Neuraxis Neuronal Dysfunction Neurons Outcome Outcome Study Pathology Patients Plant Roots Process Research Resolution Role Seizures Signal Transduction Slice Techniques Testing Therapeutic Time base behavior test extracellular fMet-Leu-Phe receptor in vivo nervous system disorder neuron loss neuronal survival novel novel strategies public health relevance receptor research study response social therapy development two-photon

项目摘要

DESCRIPTION (provided by applicant): Epilepsy represents a neurological disorder that can manifest in uncontrolled seizures in patients. Microglia are exquisitely sensitive to disruptions i the central nervous system. Since epilepsy is characterized by neuronal hyperactivity activity rooted in excessive glutamate release and ionic imbalance, it is conceivable that microglia may perform functions to reduce neuronal dysfunction and promote neuronal health during the pathology. In our preliminary studies, we have found that microglia respond by robust process extension making increasing contact with neurons during elevated glutamate levels in acute brain slices. Moreover, in three different models of epileptiform activity, microglial processes focus on neuronal dendrites and microglial ablation reduces behavioral seizure scores. Based on our preliminary results, we hypothesize that during increased glutamate levels hyperactive neurons signal to microglia inducing their process extension. Additionally, during hyperactive neuronal activity, microglial processes focus on neuronal elements with a consequence to downregulate such hyperactivity which is critical in limiting behavioral seizure outcome and promoting neuronal survival. We will now test this hypothesis along with the following specific aims. In Aim 1, we will determine the underlying mechanisms behind glutamate-induced microglial process extension elucidating the neuronal receptors initiating and the released chemoattractants mediating the process extension signal. In Aim 2, we will determine the targets of microglial process focus as well as the chemoattractants mediating the response in three models of epileptiform activity in acute brain slices. In Aim 3, we will extend our observations in acute brain slices to in vivo live brain and determine the role of microglia in epilepsy-induced seizure behaviors and neuronal cell death by microglial ablation and genetic deletion of the unique microglial P2Y12 receptor. These studies are the first to investigate the microglial dynamics during acute epilepsy. They will increase our understanding of the mechanisms underlying microglial-neuronal interactions during epileptic activity and the neuroprotective potential of microglia in epilepsy. In addition, the outcome of these studies will provide new data that could inform the development of novel therapies in the treatment of epileptic disorders.

描述（由申请人提供）：癫痫是一种神经系统疾病，可表现为患者癫痫发作不受控制。小胶质细胞对中枢神经系统的破坏非常敏感。由于癫痫的特点是神经元过度活跃，其根源是谷氨酸过度释放和离子失衡，因此可以想象，小胶质细胞可能在病理过程中发挥减少神经元功能障碍和促进神经元健康的功能。在我们的初步研究中，我们发现小胶质细胞通过强大的过程扩展做出反应，在急性脑切片中谷氨酸水平升高期间增加与神经元的接触。此外，在三种不同的癫痫样活动模型中，小胶质细胞过程集中在神经元树突上，小胶质细胞消融会降低行为癫痫评分。根据我们的初步结果，我们假设在谷氨酸水平增加期间，过度活跃的神经元向小胶质细胞发出信号，诱导其过程延伸。此外，在神经元活动过度活跃期间，小胶质细胞过程集中于神经元元件，从而下调这种过度活动，这对于限制行为癫痫结果和促进神经元存活至关重要。我们现在将测试这个假设以及以下具体目标。在目标 1 中，我们将确定谷氨酸诱导的小胶质细胞过程延伸背后的潜在机制，阐明神经元受体的启动和释放的化学引诱剂介导过程延伸信号。在目标 2 中，我们将确定小胶质细胞过程焦点的目标以及介导急性脑切片中癫痫样活动的三种模型中的反应的化学引诱剂。在目标 3 中，我们将把对急性脑切片的观察扩展到体内活体大脑，并通过小胶质细胞消融和独特的小胶质细胞 P2Y12 受体的基因删除来确定小胶质细胞在癫痫诱发的癫痫行为和神经元细胞死亡中的作用。这些研究首次调查了急性癫痫期间的小胶质细胞动力学。它们将增加我们对癫痫活动期间小胶质细胞-神经元相互作用的机制以及小胶质细胞在癫痫中的神经保护潜力的理解。此外，这些研究的结果将提供新的数据，为治疗癫痫病的新疗法的开发提供信息。