Dynamics of cerebellar Purkinje cell dendrites

小脑浦肯野细胞树突的动力学

• 批准号: 7020832
• 负责人: Anna Dunaevsky
• 金额: $ 33.53万
• 依托单位: BROWN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-05-01 至 2010-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7020832
• 关键词: cerebellar Purkinje cell; dendrites; dendritic cells; glia; neurons; receptor; role; spine

DESCRIPTION (provided by applicant): The long-term goal of this proposal is to understand the molecular and cellular mechanisms that regulate the development of cerebellar neuronal circuits. Dendritic spines, sites of synaptic input on many projection neurons such as the cerebellar Purkinje cell are highly dynamic structures and their motility is developmentally regulated. The mechanisms that regulate spine dynamics over development are not known. Here, we will use multiphoton live imaging of neuronal structures in organotypic slices and in vivo in conjunction with electron microscopy to study the mechanisms of synaptic maintenance. Our central hypothesis is that ensheathment by glial processes critically regulates dendritic spine motility and synaptic stability. In the first aim, we will characterize the development of Bergmann glia processes using static and dynamic imaging approaches. In the second aim, we will test how spine dynamics are regulated by glial ensehathment by measuring spine motility in genetic models with reduced glial ensheathment. In the third aim, we will determine the role of EphA receptors and the ephrin ligands in glia-spine cross talk and regulation of spine dynamics. Finally, we will determine how synaptic maintenance is related to spine motility and is regulated by glial processes. Abnormal development of neuronal connections can be the cause of neurodevelopmental disorders in humans. Moreover, recently it has been demonstrated that abnormal glial-neuronal interactions during development might cause mental disorders in the adult. Therefore, understanding the cellular and molecular mechanisms of glial-neuronal interactions during synapse formation and maintenance has important health significance.

描述（由申请人提供）：本提案的长期目标是了解调节小脑神经元回路发育的分子和细胞机制。树突棘是许多投射神经元（如小脑浦肯野细胞）上的突触输入部位，是高度动态的结构，其运动性受发育调节。在发育过程中调节脊柱动力学的机制尚不清楚。在这里，我们将使用多光子活体成像的神经元结构在器官型切片和在体内结合电子显微镜研究突触的维护机制。我们的中心假设是，神经胶质细胞的鞘化过程中，关键调节树突棘的运动和突触的稳定性。在第一个目标中，我们将使用静态和动态成像方法表征Bergmann神经胶质过程的发展。在第二个目标中，我们将测试脊椎动力学是如何调节神经胶质ensehathment通过测量脊椎运动的遗传模型与减少神经胶质ensheathment。在第三个目标中，我们将确定EphA受体和ephrin配体在神经胶质-脊髓串扰和脊髓动力学调节中的作用。最后，我们将确定突触的维护是如何与脊柱运动和神经胶质过程的调节。神经元连接的异常发育可能是人类神经发育障碍的原因。此外，最近已经证明，发育过程中异常的胶质-神经元相互作用可能导致成年人的精神障碍。因此，了解突触形成和维持过程中神经胶质-神经元相互作用的细胞和分子机制具有重要的健康意义。