Immune molecules in early postnatal nervous system development

描述（由申请人提供）：尽管多年来一直有证据表明免疫系统和神经系统之间存在相互作用，但免疫分子在正常发育的神经系统中具有非免疫功能的观点最近才得到证实。这一想法是基于以下观察：适应性免疫反应的主要介质，主要组织相容性复合物I类（MHCI）分子，在大脑中表达，它们介导连接的活性依赖性细化。MHCI分子也是异常或强免疫应答对发育中的大脑的影响的分子介质的有吸引力的候选物，其已经涉及几种神经发育障碍（包括自闭症和精神分裂症）的发病机制。这项提议的中心目标是确定MHCI在皮质连接最初建立期间的功能，这是一个与免疫挑战时间相当的发育阶段，可能使人类倾向于神经发育障碍。使用免疫细胞化学和组织化学，电子显微镜，细胞和切片培养和转染，一种新的长期成像分析，和全细胞膜片钳记录，我们将解决以下目标。(1)确定皮质发育过程中MHCI分子在体内和体外的定位。(2)验证MHCI分子在体内和体外调节皮质连接的初始建立和功能的假设。(3)确定MHCI分子是否通过抑制突触形成、增加突触消除或两者来负性调节皮质连接的建立。(4)验证MHCI分子通过自然杀伤细胞受体负调控皮层连接建立的假设。这项提议的结果应该揭示MHCI在典型发育中的大脑中的新功能，以及它们如何有助于大脑发育的潜在机制。 神经发育障碍

DESCRIPTION (provided by applicant): Although there has been evidence for cross-talk between the immune and nervous systems for years, the idea that immune molecules have non-immune functions in the normal developing nervous system has only recently gained credence. This idea is based on observations that the primary mediators of the adaptive immune response, major histocompatibility complex class I (MHCI) molecules, are expressed in the brain where they mediate activity-dependent refinement of connections. MHCI molecules are also attractive candidates for molecular mediators of the effects of an abnormal or strong immune response on the developing brain, which has been implicated in the pathogenesis of several neurodevelopmental disorders, including autism and schizophrenia. The central goal of this proposal is to determine the function of MHCI during the initial establishment of cortical connections, a comparable developmental stage to the time of the immune challenge that may predispose humans toward neurodevelopmental disorders. Using immunocyto- and histochemistry, electron microscopy, cell and slice culture and transfection, a novel long-term imaging assay, and whole-cell patch-clamp recording, we will address the following Aims. (1) To determine the localization of MHCI molecules in vivo and in vitro during cortical development. (2) To test the hypothesis that MHCI molecules regulate the initial establishment and function of cortical connections in vivo and in vitro. (3) To determine whether MHCI molecules negatively regulate the establishment of cortical connections by inhibiting synapse formation, increasing synapse elimination, or both. (4) To test the hypothesis that MHCI molecules act through natural killer cell receptors to negatively regulate the establishment of cortical connections. Results from this proposal should reveal novel functions of MHCI in the typically developing brain, as well as potential mechanisms for how they might contribute to neurodevelopmental disorders.