首页> 外文期刊>Cellular Physiology and Biochemistry >Therapeutic Benefit of Human Umbilical Cord Derived Mesenchymal Stromal Cells in Intracerebral Hemorrhage Rat: Implications of Anti-inflammation and Angiogenesis
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Therapeutic Benefit of Human Umbilical Cord Derived Mesenchymal Stromal Cells in Intracerebral Hemorrhage Rat: Implications of Anti-inflammation and Angiogenesis

机译:人脐带间充质基质细胞在脑出血大鼠中的治疗作用:抗炎和血管生成的意义。

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Cell-based therapy represents a promising strategy in the treatment of neurological disorders. Human umbilical cord tissue has recently been recognized as an ideal source of mesenchymal stromal cells due to accessibility, vast abundance and safety. Here, an intracerebral hemorrhage (ICH) rat model was established by injection of bacterial collagenase VII and CM-Dil labeled human umbilical cord tissue derived mesenchymal stromal cells (UC-MSC) were intracerebrally transplanted into rat brain 24h after ICH. The results demonstrated that UC-MSC treatment significantly improved neurological function deficits and decreased injury volume of ICH rats. Leukocytes infiltration, microglial activation, ROS level and matrix metalloproteinases (MMPs) production were substantially reduced in peri-ICH area in cell-treated group as compared with PBS control at day 3 post-transplantation. In addition, UC-MSC treatment significantly increased vascular density in peri-ICH area and transplanted UC-MSC were found to be able to incorporate into cerebral vasculature in ipsilateral hemisphere at 14 days after transplantation. In summary, intracerebral administration of UC-MSC could accelerate neurological function recovery of ICH rat, the underlying mechanism may ascribe to their ability to inhibit inflammation and promote angiogenesis. Thus UC-MSC may provide a potential cell candidate for cell-based therapy in neurological disorders.
机译:基于细胞的疗法代表了治疗神经系统疾病的一种有前途的策略。由于可访问性,丰富性和安全性,最近人类脐带组织被认为是间充质基质细胞的理想来源。在此,通过注射细菌胶原酶VII建立脑出血(ICH)大鼠模型,并且在ICH后24h将CM-Dil标记的人脐带组织来源的间充质基质细胞(UC-MSC)脑内移植到大鼠脑中。结果表明,UC-MSC治疗可显着改善ICH大鼠的神经功能缺陷并减少损伤量。与移植后第3天的PBS对照组相比,细胞治疗组的ICH周围区域白细胞浸润,小胶质细胞活化,ROS水平和基质金属蛋白酶(MMP)的产生显着降低。此外,UC-MSC治疗可显着增加ICH周围区域的血管密度,并且移植的UC-MSC在移植后第14天能够合并到同侧半球的脑血管中。总之,脑内给予UC-MSC可以加速ICH大鼠的神经功能恢复,其潜在机制可能归因于其抑制炎症和促进血管生成的能力。因此,UC-MSC可为神经系统疾病中基于细胞的治疗提供潜在的细胞候选物。

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