Epigenetic regulation of adult neurogenesis

成人神经发生的表观遗传调控

• 批准号: 8308419
• 负责人: Jenny Hsieh
• 金额: $ 30.63万
• 依托单位: UT SOUTHWESTERN MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-08-01 至 2014-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8308419
• 关键词: Activities of Daily Living; Adult; Applications Grants; Biochemical; Biology; Brain; Brain Injuries; Brain-Derived Neurotrophic Factor; Cell Culture Techniques; Cell Death; Cell Proliferation; Cells; Chronic; Clinical; Collaborations; Data; Development; Disease; Embryo; Environment; Epigenetic Process; Epilepsy; Epileptogenesis; Experimental Designs; Gene Expression Regulation; Gene Targeting; Generations; Genetic; Genetic Models; Genome; Goals; Health; Hippocampus (Brain); In Vitro; Individual; Injury; Kainic Acid; Knockout Mice; Knowledge; Laboratories; Lead; Learning; Measures; Mediating; Mission; Molecular; Mus; NR1 gene; Natural regeneration; Nerve Regeneration; Nerve Tissue; Nervous System Trauma; Neuronal Differentiation; Neuronal Plasticity; Neurons; Pathologic; Pharmaceutical Preparations; Physiological; Play; Process; Production; Property; Proteins; Public Health; Recovery of Function; Recurrence; Regenerative Medicine; Regulation; Research; Research Proposals; Retroviridae; Role; Seizures; Series; Signal Transduction; Specific qualifier value; Stem cells; Stimulus; Structure of germinal center of lymph node; Techniques; Testing; Time; United States; Viral Vector; Work; Zinc Fingers; adult neurogenesis; base; experience; gain of function; granule cell; improved; in vivo; innovation; insight; loss of function; migration; nerve stem cell; nervous system disorder; neurogenesis; newborn neuron; novel strategies; programs; repaired; response; skills; stem cell biology; stem cell differentiation; stem cell population; transcription factor; transcription factor REST

DESCRIPTION (provided by applicant): Seizure activity induces profound changes in stem cell proliferation and neurogenesis, yet there is a fundamental gap in understanding the mechanism of seizure-induced neurogenesis and the relationship to epilepsy. The long-term goal is to better understand the epigenetic/transcriptional circuitry important for neuronal cell fate, in both physiological and pathological contexts. The objective of this grant proposal is to elucidate the role of the master regulator of neurogenesis NRSF, in adult hippocampal neural stem cells. The central hypothesis is that seizure activity triggers the dysregulation of NRSF and selects NRSF target genes that mediate aberrant neurogenesis and epileptogenesis. The rationale for the proposed research is that understanding the mechanisms of neurogenesis after pathologic stimuli, such as seizures, has the potential to understand the underlying repair response and neuroplasticity changes after brain injury, and evaluate the suitability of stem cells for neuro-regenerative medicine. Thus, the proposed study is relevant to that part of NIH's mission that relates to gaining fundamental knowledge that will potentially help treat neurological disorders, such as epilepsy. Guided by strong preliminary data, this hypothesis will be tested by pursuing three specific aims: 1) Identify the epigenetic/transcriptional mechanism that is responsible for NRSF regulation of neuronal cell fate; 2) Determine how NRSF mediates aberrant neurogenesis after seizures using a single-cell genetic approach, and 3) Establish that NRSF contributes to seizure-induced neurogenesis and epileptogenesis using NRSF conditional knockout mice. Aims 1 and 2 will focus on the role of NRSF in neurogenesis, using gain-of-function and loss-of-function retroviral constructs to manipulate NRSF in vitro and during seizure-induced neurogenesis in vivo, which directly relate to the skills and experience in the Hsieh lab. Specific Aim 3 will be performed in collaboration with Dr. Christopher Sinton, and focus on the use of the NRSF conditional knockout mouse, to determine the role of NRSF in seizure-induced neurogenesis, and examine the contribution of aberrant neurogenesis to epileptogenesis. The approach is innovative, because it has the potential to explore the biology of adult neural stem cells and tap into their potential for cell replacement strategies after brain injury. The proposed work is significant, because it is expected to advance and expand our basic understanding of epigenetic/transcriptional regulatory mechanisms controlling neuronal cell fate after a wide range of pathologic stimuli, not just seizures. PUBLIC HEALTH RELEVANCE Disease, degeneration or traumatic injury of the nervous system are among the greatest public health concerns in the United States and are generally considered irreparable, often causing catastrophic damage to the functional capacity of the individual. Now, however, characterization of neural stem cells residing within specific germinal centers of the brain and in cell culture raises hope that functional regeneration of nervous tissue may be feasible, if we learn to exploit adult neurogenesis for clinical benefit. The research proposal will lead to improved understanding of neural stem cell biology, possibly leading to the development of new drugs for repair and regeneration of the nervous system.

描述（由申请人提供）：癫痫活动引起干细胞增殖和神经发生的深刻变化，但在了解癫痫诱导的神经发生机制及其与癫痫的关系方面存在根本差距。长期目标是更好地了解在生理和病理背景下对神经元细胞命运重要的表观遗传/转录回路。这项拨款提案的目的是阐明神经发生的主要调节剂NRSF在成人海马神经干细胞中的作用。中心假设是癫痫活动触发NRSF的失调，并选择介导异常神经发生和癫痫发生的NRSF靶基因。该研究的基本原理是，了解病理性刺激（如癫痫发作）后神经发生的机制，有可能了解脑损伤后潜在的修复反应和神经可塑性变化，并评估干细胞用于神经再生医学的适用性。因此，拟议的研究与NIH的使命有关，即获得可能有助于治疗神经系统疾病（如癫痫）的基础知识。在强有力的初步数据的指导下，这一假设将通过追求三个具体目标来验证：1)确定负责NRSF调控神经元细胞命运的表观遗传/转录机制；2)利用单细胞遗传学方法确定NRSF如何介导癫痫发作后的异常神经发生；3)利用NRSF条件敲除小鼠，确定NRSF有助于癫痫发作诱导的神经发生和癫痫发生。目标1和目标2将关注NRSF在神经发生中的作用，利用功能获得和功能丧失逆转录病毒构建体在体外和体内癫痫诱导的神经发生过程中操纵NRSF，这与Hsieh实验室的技能和经验直接相关。Specific Aim 3将与Christopher Sinton博士合作进行，重点是使用NRSF条件敲除小鼠，确定NRSF在癫痫诱导的神经发生中的作用，并检查异常神经发生对癫痫发生的贡献。这种方法是创新的，因为它有潜力探索成体神经干细胞的生物学，并挖掘它们在脑损伤后细胞替代策略的潜力。这项工作意义重大，因为它有望推进和扩展我们对广泛的病理刺激后控制神经元细胞命运的表观遗传/转录调控机制的基本理解，而不仅仅是癫痫发作。神经系统的疾病、退化或创伤性损伤是美国最大的公共卫生问题之一，通常被认为是不可修复的，通常会对个人的功能造成灾难性的损害。然而，现在，在大脑特定生发中心和细胞培养中对神经干细胞的表征提出了希望，如果我们学会利用成人神经发生用于临床利益，神经组织的功能性再生可能是可行的。这项研究计划将提高对神经干细胞生物学的理解，可能导致开发用于修复和再生神经系统的新药。