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首页> 外文期刊>Neuroreport >Adult bone marrow stromal cells administered intravenously to rats after traumatic brain injury migrate into brain and improve neurological outcome.
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Adult bone marrow stromal cells administered intravenously to rats after traumatic brain injury migrate into brain and improve neurological outcome.

机译:脑外伤后静脉内给予大鼠的成年骨髓基质细胞迁移到大脑中并改善神经功能。

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摘要

To measure effect of bone marrow stromal cells (MSCs) administered i.v. on rats subjected to traumatic brain injury (TBI), we injected MSCs labeled by BrdU into the tail vein 24 h after TBI and sacrificed rats 15 days later. The neurological severity score (NSS) and the Rotarod test were used to evaluate neurological function. The distribution of the donor cells in brain, heart, lung, kidney, liver and spleen were analyzed in recipient rats using immunohistochemical staining. MSCs injected i.v. significantly reduced motor and neurological deficits compared with control groups by day 15 after TBI. The cells preferentially entered and migrated into the parenchyma of the injured brain and expressed the neuronal marker NeuN and the astrocytic marker GFAP. MSCs were also found in other organs and primarily localized to the vascular structures, without any obvious adverse effects. Our data suggest that i.v. administration of MSCs may be useful in the treatment of TBI.
机译:为了测量静脉内施用的骨髓基质细胞(MSC)的作用。对于遭受脑外伤(TBI)的大鼠,我们在TBI后24小时将由BrdU标记的MSC注入尾静脉,并在15天后处死大鼠。使用神经系统严重程度评分(NSS)和Rotarod检验评估神经功能。使用免疫组织化学染色分析了受体大鼠中脑,心脏,肺,肾,肝和脾中供体细胞的分布。 MSC经静脉注射与对照组相比,TBI后第15天可显着减少运动和神经功能障碍。细胞优先进入并迁移到受伤的脑实质中,并表达神经元标记NeuN和星形细胞标记GFAP。 MSC也发现于其他器官中,并且主要定位于血管结构,没有任何明显的不良影响。我们的数据表明MSC的给药可能在TBI的治疗中有用。

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