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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Effects of the Insulted Neuronal Cells-Derived Extracellular Vesicles on the Survival of Umbilical Cord-Derived Mesenchymal Stem Cells following Cerebral Ischemia/Reperfusion Injury
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Effects of the Insulted Neuronal Cells-Derived Extracellular Vesicles on the Survival of Umbilical Cord-Derived Mesenchymal Stem Cells following Cerebral Ischemia/Reperfusion Injury

机译:抑制神经元细胞衍生的细胞外囊泡对脑缺血/再灌注损伤后脐带衍生间充质干细胞存活的影响

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Umbilical cord-derived mesenchymal stem cells (UC-MSCs) engraftment is a potential therapy for cerebral ischemic stroke. However, the harsh microenvironment induced by cerebral ischemia/reperfusion restricts the survival rate and therapeutic efficiency of the engrafted UC-MSCs. In this study, we explored whether small extracellular vesicles (EVs) derived from injured neuronal cells following exposure to cerebral ischemia/reperfusion insult affect the survival of transplanted UC-MSCs. To establish a simulation of cerebral ischemia/reperfusion microenvironment comprising engrafted UC-MSCs and neuronal cells, we cocultured EVs derived from injured N2A cells, caused by exposure to oxygen-glucose deprivation and reperfusion (OGD/R) insult, with UC-MSCs in a conditioned medium. Coculture of UC-MSCs with EVs exacerbated the OGD/R-induced apoptosis and oxidative stress. Suppression of EVs-release via knock-down of Rab27a effectively protected the UC-MSCs from OGD/R-induced insult. Moreover, hypoxia preconditioning not only elevated the survival of UC-MSCs but also improved the paracrine mechanism of injured N2A cells. Altogether, these results show that EVs from injured N2A cells exacerbates OGD/R-induced injury on transplanted UC-MSCs in vitro. Hypoxia preconditioning enhances the survival of the engrafted-UC-MSCs; hence, thus could be an effective approach for improving UC-MSCs therapy in ischemic stroke.
机译:脐带衍生的间充质干细胞(UC-MSCs)植入是脑缺血性卒中的潜在疗法。然而,通过脑缺血/再灌注诱导的苛刻微环境限制了植入的UC-MSCs的存活率和治疗效率。在这项研究中,我们探讨了在暴露于脑缺血/再灌注损伤后衍生自受损神经元细胞的小细胞外囊泡(EVS)影响移植的UC-MSCs的存活。建立脑缺血/再灌注微环境的模拟,包括植入的UC-MSC和神经元细胞,通过暴露于氧 - 葡萄糖剥夺和再灌注(OGD / R)损伤引起的患有受损的N2A细胞的EV,与UC-MSC一起引起条件介质。具有EVS的UC-MSC的共培养加剧了OGD / R诱导的细胞凋亡和氧化应激。通过Rab27a的敲除抑制EVS释放有效地保护了来自OGD / R引起的损伤的UC-MSC。此外,缺氧预处理不仅升高了UC-MSC的存活率,而且还改善了受伤的N2A细胞的旁静脉机制。总之,这些结果表明,受损N2A细胞的EVS加剧了OGD / R诱导的体外移植UC-MSC的损伤。缺氧预处理增强了植入 - UC-MSCs的存活;因此,因此可能是改善缺血性卒中中的UC-MSCs治疗的有效方法。

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