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首页> 外文期刊>Mechanisms of Ageing and Development >Infiltrating macrophages contribute to age-related neuroinflammation in C57/BL6 mice
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Infiltrating macrophages contribute to age-related neuroinflammation in C57/BL6 mice

机译:渗透巨噬细胞在C57 / BL6小鼠中有助于年龄相关的神经炎症

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The recognized role of neuroinflammation in the age-related deterioration of neuronal function highlights the importance of understanding the factors that control microglial activation. Microglia, as the immune cells of the brain, are the arbiters of the inflammatory profile in the brain. Normally they are maintained in a quiescent state by means of ligand-receptor interactions with neurons, within a prevailing anti-inflammatory microenvironment. The evidence indicates that, as the ageing process continues, microglia become activated, shift towards an inflammatory phenotype and alter the milieu in the brain. Although there has been progress in identifying factors that contribute to age-related microglial activation, our understanding remains incomplete. Here we report that there was an age-related increase in circulating inflammatory cytokines, accompanied by microglial activation. Neutrophils, and to a greater extent, macrophages, infiltrate the brain with age, perhaps as a result of increased chemokine expression in the brain, specifically CXCL1 and CCL2. We sought to determine whether macrophages might trigger microglial activation and the evidence shows that conditioned medium obtained from interferon-gamma (IFN gamma)-stimulated macrophages potently activated microglia. The data suggest that infiltrating macrophages may be one factor that contributes to age-related microglial activation.
机译:神经引发在神经元函数的年龄相关恶化中的公认作用凸显了理解控制微胶质激活的因素的重要性。作为大脑的免疫细胞的微胶质细胞是脑内炎症性曲线的仲裁者。通常,通过与神经元的配体 - 受体相互作用,在普遍的抗炎微环境中,它们保持静止状态。证据表明,随着衰老过程的持续,小胶质细胞被激活,转向炎症表型并改变大脑中的Milieu。虽然在识别有助于年龄与年龄相关的微胶质激活的因素方面取得了进展,但我们的理解仍然不完整。在这里,我们报告说循环炎性细胞因子伴随着显微胶质激活有关的增长。中性粒细胞,以及更大程度的巨噬细胞,随着年龄的增长渗透脑,可能是大脑中的趋化因子表达增加,特别是CXCL1和CCL2。我们试图确定巨噬细胞是否可能引发小胶质激活,并且证据表明,从干扰素-γ(IFNγ) - 刺激的巨噬细胞获得的调理培养基均可激活的微胶质。数据表明,渗透巨噬细胞可能是有助于年龄相关的微胶质激活的一个因素。

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