Reelin regulation of the crosstalk between the Immune and Nervous systems

大脑和免疫系统很容易对多种内部和外部信号做出反应，并随着这些经历而适应和改变。此外，免疫系统和大脑显然相互影响，这种串扰也对它们的可塑性和行为产生影响。我的一般研究计划侧重于研究免疫和神经可塑性的机制，以及这些机制如何影响大脑和免疫系统功能以及两个系统之间的相互作用。在这个建议中，我将评估的假设，reelin，细胞外基质蛋白质表达在脑和血浆中，起着重要的作用，在调节免疫和神经可塑性，并促进两个系统之间的串扰。Reelin首先被鉴定为脑发育中的关键蛋白质，此后，它被证明可以调节成人脑中GABA能和谷氨酸能系统之间的相互作用以及神经可塑性。除了大脑，reelin也在血浆和淋巴细胞中表达，并且具有reelin缺陷的动物似乎在其免疫系统中显示出显著的改变。然而，目前还没有系统的研究来研究reelin如何影响免疫系统或大脑与免疫系统之间的串扰。我最近的工作已经开始解决这个问题。我们已经表明，糖皮质激素影响reelin表达在特定的大脑区域，也是reelin赤字带来的改变，在血淋巴细胞膜蛋白聚集。为了直接评估的潜在作用，reelin在调节神经和免疫串扰，我提出了一系列的实验，旨在分析reelin下调的神经递质受体和转运蛋白位于大脑和免疫系统的表达和膜簇的影响，和细胞因子的释放（特别是在大脑和外周观察到的细胞因子）。在体内系统的情况下，我还将研究与reelin缺陷相关的认知行为的改变（即物体识别测试）。我还建议管理重组reelin的动物，其中reelin赤字已引起无论是遗传或通过应用糖皮质激素。在这种情况下，我计划评估重组reelin的管理是否可以恢复大脑和免疫可塑性以及行为的变化，我们希望在reelin缺陷动物中看到。

The brain and immune system readily respond to multiple internal and external signals and adapt and change with these experiences. In addition, the immune system and the brain clearly influence each other, and this crosstalk also has an effect in their plasticity and behavior. My general research program focuses on studying the mechanisms underlying immune and neural plasticity, and how these mechanisms affect the brain and immune system functions and the interactions between both systems. In this proposal, I will evaluate the hypothesis that reelin, an extracellular matrix protein expressed both in brain and blood plasma, plays an important role in regulating immune and neural plasticity and in facilitating the crosstalk between both systems. Reelin was first identified as a critical protein in brain development, and thereafter it was shown to regulate neural plasticity and the interaction between GABAergic and glutamatergic systems in the adult brain. In addition to the brain, reelin is also expressed in blood plasma and lymphatic cells, and animals with reelin deficiencies appear to show prominent alterations in their immune system. However, there has been no systematic investigation of how reelin influences the immune system or the crosstalk between the brain and the immune system. My recent work has begun to address this issue. We have shown that glucocorticoids affect reelin expression in specific brain regions and also that reelin deficits bring about alterations in membrane protein clustering in blood lymphocytes. To directly assess the potential role of reelin in regulating neural and immune crosstalk, I propose a series of experiments designed to analyze the effects of reelin downregulation on the expression and membrane clustering of neurotransmitter receptors and transporters located both in brain and the immune system, and on the release of cytokines (particularly on cytokines that are observed both in the brain and periphery). In the case of the in vivo system, I will also study alterations in cognitive behavior associated with reelin deficits (i.e. object recognition test). I also propose to administer recombinant reelin to animals where a reelin deficit has been induced either genetically or through the application of glucocorticoids. In this case, I plan to assess whether the administration of recombinant reelin can restore the alterations in brain and immune plasticity and also on behavior, that we expect to see in reelin-deficit animals.