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星形胶质细胞靶向表达白细胞介素-10 的转基因小鼠中小胶质细胞表型和海马神经元功能的改变。

Alterations in microglial phenotype and hippocampal neuronal function in transgenic mice with astrocyte-targeted production of interleukin-10.

机构信息

Department of Cell Biology, Physiology and Immunology, Institute of Neuroscience, Universitat Autònoma de Barcelona, Bellaterra 08193, Spain.

Department of Cell Biology, Physiology and Immunology, Institute of Neuroscience, Universitat Autònoma de Barcelona, Bellaterra 08193, Spain.

出版信息

Brain Behav Immun. 2015 Mar;45:80-97. doi: 10.1016/j.bbi.2014.10.015. Epub 2014 Oct 31.

Abstract

Interleukin-10 (IL-10) is a cytokine classically linked with anti-inflammatory and protective functions in the central nervous system (CNS) in different neurodegenerative and neuroinflammatory conditions. In order to study the specific role of local CNS produced IL-10, we have created a new transgenic mouse line with astrocyte-targeted production of IL-10 (GFAP-IL10Tg). In the present study, the effects of local CNS IL-10 production on microglia, astrocytes and neuronal connectivity under basal conditions were investigated using immunohistochemistry, molecular biology techniques, electrophysiology and behavioural studies. Our results showed that, in GFAP-IL10Tg animals, microglia displayed an increase in density and a specific activated phenotype characterised by morphological changes in specific areas of the brain including the hippocampus, cortex and cerebellum that correlated with the level of transgene expressed IL-10 mRNA. Distinctively, in the hippocampus, microglial cells adopted an elongated morphology following the same direction as the dendrites of pyramidal neurons. Moreover, this IL-10-induced microglial phenotype showed increased expression of certain molecules including Iba1, CD11b, CD16/32 and F4/80 markers, "de novo" expression of CD150 and no detectable levels of either CD206 or MHCII. To evaluate whether this specific activated microglial phenotype was associated with changes in neuronal activity, the electrophysiological properties of pyramidal neurons of the hippocampus (CA3-CA1) were analysed in vivo. We found a lower excitability of the CA3-CA1 synapses and absence of long-term potentiation (LTP) in GFAP-IL10Tg mice. This study is the first description of a transgenic mouse with astrocyte-targeted production of the cytokine IL-10. The findings indicate that IL-10 induces a specific activated microglial phenotype concomitant with changes in hippocampal LTP responses. This transgenic animal will be a very useful tool to study IL-10 functions in the CNS, not only under basal conditions, but also after different experimental lesions or induced diseases.

摘要

白细胞介素-10(IL-10)是一种细胞因子,在不同的神经退行性和神经炎症性疾病中与中枢神经系统(CNS)的抗炎和保护功能有关。为了研究局部中枢神经系统产生的 IL-10 的特定作用,我们创建了一种新的转基因小鼠系,该系具有星形胶质细胞靶向产生 IL-10(GFAP-IL10Tg)的能力。在本研究中,使用免疫组织化学、分子生物学技术、电生理学和行为学研究,研究了局部 CNS IL-10 产生对小胶质细胞、星形胶质细胞和神经元连接的影响。我们的结果表明,在 GFAP-IL10Tg 动物中,小胶质细胞的密度增加,并表现出特定的激活表型,其特征在于包括海马体、皮质和小脑在内的大脑特定区域的形态变化,这与转基因表达的 IL-10 mRNA 水平相关。值得注意的是,在海马体中,小胶质细胞呈现出与锥体神经元树突相同方向的伸长形态。此外,这种由 IL-10 诱导的小胶质细胞表型显示出某些分子的表达增加,包括 Iba1、CD11b、CD16/32 和 F4/80 标志物、CD150 的“新”表达,以及检测不到 CD206 或 MHCII 的水平。为了评估这种特定的激活小胶质细胞表型是否与神经元活动的变化有关,我们在体内分析了海马体(CA3-CA1)锥体神经元的电生理特性。我们发现 GFAP-IL10Tg 小鼠 CA3-CA1 突触的兴奋性降低,并且不存在长时程增强(LTP)。本研究首次描述了一种具有星形胶质细胞靶向产生细胞因子 IL-10 的转基因小鼠。研究结果表明,IL-10 诱导特定的激活小胶质细胞表型,同时伴有海马体 LTP 反应的变化。这种转基因动物将是研究 IL-10 在中枢神经系统中的功能的非常有用的工具,不仅在基础条件下,而且在不同的实验性损伤或诱导性疾病后也是如此。

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