Cell Identity Determination In Cerebral Cortex

大脑皮层细胞身份测定

• 批准号: 8132953
• 负责人: Christopher A. Walsh
• 金额: $ 37.27万
• 依托单位: BOSTON CHILDREN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 1994
• 资助国家: 美国
• 起止时间: 1994-12-16 至 2014-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8132953
• 关键词: Adult; Age; Bathing; Biological Assay; Brain; Cells; Cerebral Palsy; Cerebral cortex; Cerebrospinal Fluid; Cerebrum; Cilia; Conscious; Craniocerebral Trauma; Cues; Data; Development; Embryo; Embryonic Development; Epilepsy; Failure; Funding; Genes; Goals; Grant; Growth Factor; Human; Human Development; IGF2 gene; Immune Sera; Immunoblotting; In Vitro; Learning Disorders; Mass Spectrum Analysis; Memory; Mental Retardation; Microcephaly; Mitotic spindle; Mus; Natural regeneration; Nature; Neurons; Pattern; Pharmaceutical Preparations; Play; Proliferating; Proteins; Proteome; Regulation; Role; Series; Signal Transduction; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Stem cells; Stroke; Testing; Therapeutic; Time; Tissues; Work; age related; case control; cognitive function; embryonic protein; improved; mind control; mouse model; nerve stem cell; nervous system disorder; neuroepithelium; neurogenesis; neuroregulation; protein transport; public health relevance; receptor; research study; response; stem cell niche

DESCRIPTION (provided by applicant): The major goal of this proposal is to elucidate basic cellular mechanisms of neurogenesis, and to understand the mechanisms that control the ability of neural stem cells to survive and proliferate. Proper development of the cerebral cortex is essential for normal cognitive function, and requires the precise completion of a series of developmental steps. Abnormalities of cerebral cortical development can cause mental retardation, epilepsy, learning disorders, and cerebral palsy. In the previous funding period of this grant we studied of the mechanisms of several causes of microcephaly (small cerebral cortex), these studies suggest that microcephaly genes play important roles in the control of neural proliferation and, in some cases, the control of neural cell fate. In this grant we propose to analyze the stem cell niche that regulates neural stem cells in the developing, and the adult, brain. These experiments have profound significance for elucidating the fundamental control of neural stem cells in the brain, and have potential therapeutic implications in improving our ability to control these stem cells. We propose to study the regulation of neurogenesis by the embryonic cerebral spinal fluid (eCSF) proteome. Although many genes that regulate neurogenesis have been identified, the global controls that initiate and terminate neurogenesis are completely unknown. Our preliminary data suggest that eCSF, which bathes the cilia of all known neural stem cells both during development and in adulthood, shows instructive effects on neurogenesis in cortical explants and cultured neural stem cells that differ with the age of the explant, and the age of the eCSF. We propose to analyze the effects of eCSF on cerebral cortical explants in vitro and cultured neural stem cells in vitro and age-related changes in the effects of eCSF (and adult CSF) on cortical explants and cultured neural stem cells. We further propose to identify and verify eCSF components that regulate cortical neurogenesis. The pace and nature of neurogenesis changes rapidly in the last days of embryonic development suggesting that global cues change as well. Our preliminary data show that the functional effects and protein composition of CSF changes dramatically during this same time-frame. To study this we will use MALDI-mass spectroscopy and Western analysis to determine the composition of the CSF proteome during the period of cortical neurogenesis, and analyze changes in concentration of key CSF components. We will also study the regulation of neurogenesis by specific proteins of the eCSF. We have identified IGF2 as one specific growth factor that is highly expressed in eCSF during neurogenesis, and down regulated postnatally. We propose to analyze the effects of gain and loss IGF2 and other specific eCSF proteins on neurogenesis. PUBLIC HEALTH RELEVANCE: Proper development of the cerebral cortex (the portion of the brain that controls higher functions such as memory and consciousness) is essential for normal cognitive function, and requires the precise completion of a series of developmental steps. Abnormalities of cerebral cortical development can cause mental retardation, epilepsy, learning disorders, and cerebral palsy. The experiments proposed in this grant have profound significance for elucidating the fundamental control of neural stem cells (cells that will become neurons) in the brain, and have potential therapeutic implications in improving our ability to control these stem cells.

描述（由申请人提供）：本提案的主要目标是阐明神经发生的基本细胞机制，并了解控制神经干细胞存活和增殖能力的机制。大脑皮层的正常发育对正常的认知功能至关重要，需要精确完成一系列发育步骤。大脑皮层发育异常可引起智力低下、癫痫、学习障碍和脑瘫。在该资助的前一个资助期，我们研究了几种导致小头畸形（小大脑皮层）的机制，这些研究表明，小头畸形基因在控制神经增殖中发挥重要作用，在某些情况下，控制神经细胞的命运。在这项资助中，我们建议分析调节发育中和成人大脑中神经干细胞的干细胞生态位。这些实验对于阐明大脑中神经干细胞的基本控制具有深远的意义，并且在提高我们控制这些干细胞的能力方面具有潜在的治疗意义。 我们建议研究胚胎脑脊髓液（eCSF）蛋白质组的神经发生的调节。虽然许多调节神经发生的基因已经被鉴定，但启动和终止神经发生的全局控制是完全未知的。我们的初步数据表明，eCSF，沐浴所有已知的神经干细胞的纤毛在发展过程中，并在成年期，显示出不同的年龄的外植体和培养的神经干细胞的皮层外植体的神经发生的指导作用，和年龄的eCSF。我们建议分析eCSF对体外大脑皮层外植体和体外培养的神经干细胞的影响，以及eCSF（和成人CSF）对皮层外植体和培养的神经干细胞的影响的年龄相关变化。 我们进一步提出，以确定和验证eCSF组件，调节皮质神经发生。神经发生的速度和性质在胚胎发育的最后几天迅速变化，这表明全球线索也发生了变化。我们的初步数据表明，CSF的功能效应和蛋白质组成在同一时间范围内发生了显着变化。为了研究这一点，我们将使用MALDI-质谱和Western分析来确定皮质神经发生期间CSF蛋白质组的组成，并分析关键CSF组分浓度的变化。 我们还将研究eCSF的特定蛋白对神经发生的调节。我们已经确定IGF 2是一种特异性生长因子，在神经发生过程中在eCSF中高度表达，并在出生后下调。我们建议分析IGF 2和其他特定eCSF蛋白的获得和损失对神经发生的影响。 公共卫生关系：大脑皮层（大脑中控制记忆和意识等高级功能的部分）的适当发育对正常的认知功能至关重要，需要精确完成一系列发育步骤。大脑皮层发育异常可引起智力低下、癫痫、学习障碍和脑瘫。这项资助中提出的实验对于阐明大脑中神经干细胞（将成为神经元的细胞）的基本控制具有深远的意义，并在提高我们控制这些干细胞的能力方面具有潜在的治疗意义。