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T‐cells and macrophages peak weeks after experimental stroke: Spatial and temporal characteristics

机译:实验中风后的T细胞和巨噬细胞高峰周:空间和时间特征

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The activities of the central and peripheral immune systems impact neurological outcome after ischemic stroke. However, studies investigating the temporal profile of leukocyte infiltration, especially T‐cell recruitment, are sparse. Our aim was to investigate leukocyte infiltration at different time points after experimental stroke in mice. Permanent middle cerebral artery occlusion was performed on 11?weeks old C57BL/6J mice, allowed to survive for 1, 3, 8, 14 or 28?days. In addition to infarct size measurements, detailed immunohistochemical analyses of T‐cell and macrophage influx were performed. A recently introduced F‐19 MR probe (V‐sense), designed to track macrophages, was furthermore tested. Fourteen and 28 days after permanent middle cerebral artery occlusion a significant increase in CD3 + T‐cells was found within the ipsilateral hemisphere compared to controls, especially within the infarct core and the corpus callosum. The number of CD68 + cells within the infarct core was significantly increased at days 8, 14 and 28. This temporal pattern was also seen in MRI. After experimental stroke within the infarcted cortex we found a delayed (day 14) infiltration of T‐cells and macrophages. Furthermore, our data show that T‐cells are present in higher numbers in the corpus callosum compared to the rest of the brain (except from the infarct core where they were highest).
机译:中枢和外周免疫系统的活动会影响缺血性中风后神经结果。然而,研究研究白细胞浸润,尤其是T细胞募集的时间曲线的研究是稀疏的。我们的目的是在小鼠实验中风后调查不同时间点的白细胞浸润。在11个左右的C57BL / 6J小鼠中进行永久性中间脑动脉闭塞,使其存活1,3,8,14或28个月。除梗塞尺寸测量外,还进行详细的T细胞和巨噬细胞流入的免疫组化分析。此外,最近引入的F-19 MR探针(V型),设计用于跟踪巨噬细胞。与对照组相比,在Ipsilatal Hemisphere中发现CD3 + T细胞的显着增加了14天和28天。在第8,14和28天,梗塞核心的CD68 +细胞的数量显着增加。在MRI中也观察到这种时间模式。在梗死的皮质内进行实验中风后,我们发现延迟(第14天)T细胞和巨噬细胞浸润。此外,我们的数据表明,与大脑的其余部分相比

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