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首页> 外文期刊>Iranian Journal of Basic Medical Sciences >THERAPEUTIC BENEFIT OF INTRAVENOUS ADMINISTRATION OF HUMAN UMBILICAL CORD BLOOD- MONONUCLEAR CELLS FOLLOWING INTRACEREBRAL HEMORRHAGE IN RAT
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THERAPEUTIC BENEFIT OF INTRAVENOUS ADMINISTRATION OF HUMAN UMBILICAL CORD BLOOD- MONONUCLEAR CELLS FOLLOWING INTRACEREBRAL HEMORRHAGE IN RAT

机译:大鼠脑室内出血后静脉给药对人脐带血-单核细胞的治疗益处

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Objective(s): Human umbilical cord blood (HUCB) is now considered as a valuable source for stem cell–based therapies. Previous studies showed that intravascular injection of the HUCB significantly improves neurological functional recovery in a rat model of intracerebral hemorrhage (ICH). In the present study, we hypothesize transplanted HUCB derived mononuclear cells (UC-MCs) can decrease injured volume and also ameliorate neurological function in ICH rats. Materials and Methods: Experimental ICH was induced by intrastriatal administration of collagenase in rats. One day after surgery, the rats were divided into 3 groups to receive intravenously either BrdU positive human UC-MCs [(4×106 and 8×106 cells in 1 ml saline, n=10 respectively) as treated groups] or the same amount of saline [as lesion group (n=10)]. There was also one group (control) that received only vehicle solution of collagenase. The animals were evaluated for 14 days with behavioral tests. Transplanted UC-MCs were detected by immunohistochemistry. Histological data and scores of functional tests were analyzed using ANOVA. Cellular co-localization of BrdU+ cells in the histological slides was determined by software Image J. Results: Intravenously transplanted UC-MCs migrated selectively to the hematomal area and reduce injured volume. The UC-MCs transplanted groups showed better performance on functional tests after 2 weeks compared with the lesion and control groups (PConclusion: Intravenously transplanted UC-MCs accelerate neurological function recovery of ICH rat and diminish the striatum lesion size. Thus these cells may provide a potential cell candidate for cell-based therapy in ICH.
机译:目标:人脐带血(HUCB)现在被认为是基于干细胞疗法的宝贵来源。先前的研究表明,HUCB的血管内注射可显着改善大鼠脑出血(ICH)模型的神经功能恢复。在本研究中,我们假设移植的HUCB衍生单核细胞(UC-MCs)可以减少ICH大鼠的受伤体积并改善其神经功能。材料与方法:实验性脑出血是通过纹状体内给予胶原酶诱导的。手术后一天,将大鼠分成3组,分别静脉内接受BrdU阳性人UC-MCs [(4×10 6 和8×10 6 每毫升生理盐水,分别为n = 10(作为治疗组)或相同量的生理盐水[与病变组(n = 10)]。还有一组(对照组)仅接受胶原酶的载体溶液。通过行为测试评估动物14天。通过免疫组织化学检测移植的UC-MC。使用ANOVA分析组织学数据和功能测试的分数。通过软件Image J确定组织学玻片中BrdU +细胞的细胞共定位。结果:静脉移植的UC-MCs选择性迁移至血肿区域并减少了损伤体积。与病变和对照组相比,UC-MCs移植组在2周后的功能测试中表现出更好的性能(PConclusion:静脉移植的UC-MC可以加速ICH大鼠的神经功能恢复,并减少纹状体病变的大小。因此,这些细胞可以提供ICH中基于细胞的治疗的潜在候选细胞。

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