首页> 外文期刊>Journal of Neuroscience Research >Transplantation with Hypoxia-preconditioned Mesenchymal Stem Cells Suppresses Brain Injury Caused by Cardiac Arrest-induced Global Cerebral Ischemia in Rats
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Transplantation with Hypoxia-preconditioned Mesenchymal Stem Cells Suppresses Brain Injury Caused by Cardiac Arrest-induced Global Cerebral Ischemia in Rats

机译:用缺氧预处理的间充质干细胞移植抑制了大鼠心脏滞留诱导的全球脑缺血引起的脑损伤

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摘要

Cardiac arrest-induced global cerebral ischemia is a main cause of neurological dysfunction in emergency medicine. Transplantation with bone marrow mesenchymal stem cells (MSCs) has been used in stroke models to repair the ischemic brain injury, but it is little studied in models with global cerebral ischemia. In the present study, a hypoxia precondition was used to improve the efficacy of MSC transplantation, given the low survival and migration rates and limited differentiation capacities of MSCs. We found that hypoxia can increase the expansion and migration of MSCs by activating the PI3K/AKT and hypoxia-inducible factor-1 alpha/CXC chemokine receptor-4 pathways. By using a cardiac arrest-induced global cerebral ischemic model in rats, we found that transplantation of hypoxia-preconditioned MSCs promoted the migration and integration of MSCs and decreased neuronal death and inflammation in the ischemic cortex. (C) 2017 Wiley Periodicals, Inc.
机译:心脏抑制诱导的全球性脑缺血是急诊医学中神经功能障碍的主要原因。 用骨髓间充质干细胞(MSCs)移植已用于中风模型以修复缺血性脑损伤,但在全球脑缺血的模型中很少研究。 在本研究中,鉴于MSC的低生存和迁移率和有限的分化能力,用于改善MSC移植的功效和MSCs的有限分化能力。 我们发现缺氧可以通过激活PI3K / AKT和缺氧诱导因子-1α/ CXC趋化因子受体-4途径来增加MSC的膨胀和迁移。 通过在大鼠中使用心脏滞留诱导的全球性脑缺血模型,我们发现缺氧预处理MSC的移植促进了MSCs的迁移和整合,并且在缺血皮层中减少了神经元死亡和炎症。 (c)2017 Wiley期刊,Inc。

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