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HIF-1α confers resistance to induced stress in bone marrow-derived mesenchymal stem cells

机译:HIF-1α赋予骨髓间充质干细胞对诱导应激的抗性

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Background and Aims: The major limiting factor in therapeutic application of mesenchymal stem cells (MSCs) is their high vulnerability during the early days of transplantation. Hence, researchers have been encouraged to find various strategies to make the cells resistant to different stresses before and after transplantation. Overexpression of HIF-1α in MSCs to confer resistance against harmful conditions was the aim of this study. Methods: Using an in vitro approach, we engineered MSCs to overexpress HIF-1α and then evaluated their viability following exposure to hypoxic and oxidative stresses. The inherent expression of HIF-1α was downregulated by siRNA. Viability and apoptosis of the MSCs were then evaluated in vitro following their exposure to hypoxic and oxidative stress conditions. Results: Whereas overexpression of HIF-1α in MSCs was protective against cell death and apoptosis triggered by hypoxic and oxidative stress conditions, its downregulation increased apoptosis and death rate. Conclusions: Our study is the first to demonstrate how human MSCs can be manipulated to gain protection against stresses that potentially limit their clinical application.
机译:背景与目的:间充质干细胞(MSCs)在治疗中的主要限制因素是它们在移植初期的高度脆弱性。因此,已经鼓励研究人员寻找各种策略来使细胞在移植前后具有不同的抵抗力。本研究的目的是在MSC中过表达HIF-1α以赋予其对有害条件的抗性。方法:使用体外方法,我们设计了MSCs过表达HIF-1α,然后评估了其在低氧和氧化胁迫下的生存能力。 siRNA下调了HIF-1α的固有表达。然后,在暴露于低氧和氧化应激条件下,对MSC的存活力和凋亡进行体外评估。结果:MSC中HIF-1α的高表达可防止由缺氧和氧化应激条件引起的细胞死亡和凋亡,而其下调则增加了细胞凋亡和死亡率。结论:我们的研究首次证明了如何操纵人类MSC来抵御可能限制其临床应用的压力。

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