Typical and Pathological Cellular Development of the Human Amygdala

人类杏仁核的典型和病理性细胞发育

• 批准号: 8325656
• 负责人: Cynthia Schumann
• 金额: $ 38.5万
• 依托单位: UNIVERSITY OF CALIFORNIA AT DAVIS
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-01 至 2016-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8325656
• 关键词: Adolescent; Adult; Age; Age-Years; Amygdaloid structure; Apoptosis; Autistic Disorder; Autopsy; Biological; Brain; Cell Count; Cell Nucleus; Cell physiology; Cells; Cessation of life; Child; Childhood; Data; Defect; Dendrites; Development; Disease; Goals; Golgi Apparatus; Growth; Human; Immunohistochemistry; Individual; Knowledge; Lateral; Life; Magnetic Resonance Imaging; Maps; Measures; Mental disorders; Microglia; Nerve Degeneration; Neurodevelopmental Disorder; Neuroglia; Neurons; Outcome; Pathology; Population; Process; Property; Publishing; Reporting; Research; Sampling; Sensory; Structure; Therapeutic; Vertebral column; age group; autistic children; base; brain tissue; case control; cellular development; density; indexing; neurogenesis; neuroinflammation; neuron apoptosis; neuronal cell body; neuropathology; novel strategies; programs; relating to nervous system; research study; therapy development

DESCRIPTION (provided by applicant): Amygdala structure and function are abnormal in a remarkable number of neurodevelopmental and psychiatric disorders. However, the normal cellular development of the human amygdala remains almost entirely unstudied. As a result, there is no baseline information that can be used to identify the cellular alterations that are associated with these disorders. Autism is one of the most common neurodevelopmental disorders and is marked by profound changes in the growth of the amygdala in the first years of life. However, there have been no quantitative, postmortem studies of the cellular features underlying these early structural changes in young children with autism. In the only quantitative postmortem study of the amygdala published to date, we found that in adults with autism, neuron number is reduced. Interestingly, these alterations are most robust in the lateral (sensory input) nucleus of the amygdala. However, the cellular processes that create this diminished neuronal population remain unknown. Thus, the overarching goal of this proposal is to define the cellular maturation of the human amygdala from childhood to adulthood in typical development and contrast this cellular profile with developmental trajectory of the amygdala in individuals with autism. We will also explore what neural defects and disease states might produce pathological changes in cell populations in autism. Our research program will examine the amygdala from 80 postmortem brains (40 autism, 40 control) equally distributed across the age range of 2-40 years. We will employ a novel approach to conducting studies of human brain tissue by carrying out multiple experiments, including quantitative stereology to estimate neuron and glia numbers, Golgi impregnation to assess dendritic maturation, and immunohistochemistry to assess neuroinflammation and neurodegeneration within the same subject. This approach not only allows us to maximize the amount of knowledge we can gain from every brain donation, but also to examine the relationships between multiple cellular features. This research program will be the first to comprehensively describe the cellular maturation of the human amygdala from childhood to adulthood, representing a major advance in our understanding of the cellular properties of the typically developing human brain and completing a critical first step in examining the origins of many neurodevelopmental and psychiatric disorders. The program will also be the first to quantitatively examine cellular alterations in the brain in children with autism, enhancing our understanding of the developmental neuropathology of this disorder and pointing the way towards targets for effective biological therapeutics.

描述（由申请人提供）：杏仁核结构和功能在大量神经发育和精神疾病中出现异常。然而，人类杏仁核的正常细胞发育几乎完全未被研究。因此，没有可用于识别与这些疾病相关的细胞改变的基线信息。自闭症是最常见的神经发育障碍之一，其特点是生命最初几年杏仁核生长的深刻变化。然而，目前还没有对自闭症幼儿早期结构变化背后的细胞特征进行定量、尸检研究。在迄今为止发表的唯一一项针对杏仁核的定量死后研究中，我们发现患有自闭症的成年人的神经元数量减少。有趣的是，这些改变在杏仁核的外侧（感觉输入）核中最为强烈。然而，导致神经元数量减少的细胞过程仍然未知。因此，该提案的首要目标是定义典型发育中人类杏仁核从童年到成年的细胞成熟，并将这种细胞特征与自闭症个体杏仁核的发育轨迹进行对比。我们还将探讨哪些神经缺陷和疾病状态可能会导致自闭症细胞群发生病理变化。我们的研究计划将检查 80 个死后大脑（40 个自闭症患者，40 个对照）的杏仁核，这些大脑均匀分布在 2-40 岁的年龄范围内。我们将采用一种新颖的方法通过进行多项实验来进行人类脑组织的研究，包括定量体视学来估计神经元和神经胶质细胞的数量，高尔基体浸渍来评估树突成熟，以及免疫组织化学来评估同一受试者的神经炎症和神经变性。这种方法不仅使我们能够最大限度地从每次大脑捐赠中获得知识，而且还可以检查多个细胞特征之间的关系。该研究计划将是第一个全面描述人类杏仁核从童年到成年的细胞成熟过程的研究项目，代表着我们对典型发育的人类大脑的细胞特性的理解取得了重大进展，并完成了研究杏仁核起源的关键的第一步。许多神经发育和精神疾病。该计划也将是第一个定量检查自闭症儿童大脑细胞变化的项目，增强我们对这种疾病的发育神经病理学的理解，并为有效的生物治疗目标指明道路。