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Lipocalin-2-mediated upregulation of various antioxidants and growth factors protects bone marrow-derived mesenchymal stem cells against unfavorable microenvironments

机译:脂质2介导的各种抗氧化剂和生长因子的上调保护骨髓来源的间充质干细胞免受不利的微环境的侵害

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摘要

Despite many advantages of mesenchymal stem cells (MSCs) that make them suitable for cell therapy purposes, their therapeutic application has been limited due to their susceptibility to several stresses (e.g., nutrient-poor environment, oxidative stress, and hypoxic and masses of cytotoxic factors) to which they are exposed during their preparation and following transplantation. Hence, reinforcing MSCs against these stresses is a challenge for both basic and clinician scientists. Recently, much attention has been directed toward equipping MSCs with cytoprotective factors to strengthen them against unfavorable microenvironments. Here, we engineered MSCs with lipocalin 2 (Lcn2), a cytoprotective factor that is naturally induced following exposure of cells to stresses imposed by the microenvironment. Lcn2 overexpression not only did not interfere with the multidifferentiation capacity of the MSCs but also granted many protective properties to them. Lcn2 potentiated MSCs to withstand oxidative, hypoxia, and serum deprivation (SD) conditions via antagonizing their induced cytotoxicity and apoptosis. Adhesion rate of MSCs to coated culture plates was also enhanced by Lcn2 overexpression. In addition, Lcn2 induced antioxidants and upregulated some growth factors in MSCs. Our findings suggested a new strategy for prevention of graft cell death in MSC-based cell therapy.Electronic supplementary materialThe online version of this article (doi:10.1007/s12192-013-0430-2) contains supplementary material, which is available to authorized users.
机译:尽管间充质干细胞(MSC)具有许多优势,使其适合用于细胞治疗,但由于它们对多种压力(例如营养不良的环境,氧化应激,低氧和大量细胞毒性因子)的敏感性,其治疗应用受到了限制。 )在准备过程中和移植后暴露于其中。因此,增强MSC抵抗这些压力对于基础和临床科学家都是一个挑战。近来,已经将许多注意力集中在装备具有细胞保护因子的MSC上,以增强它们抵抗不利的微环境的能力。在这里,我们用脂环蛋白2(Lcn2)设计了MSC,脂环蛋白2(Lcn2)是一种细胞保护因子,在细胞暴露于微环境施加的压力后自然诱导。 Lcn2的过表达不仅不干扰MSC的多分化能力,而且还赋予它们许多保护特性。 Lcn2增强的MSC通过拮抗诱导的细胞毒性和凋亡来抵抗氧化,缺氧和血清剥夺(SD)条件。 Lcn2的过表达也增强了MSCs对包被的培养板的粘附率。此外,Lcn2诱导抗氧化剂并上调MSC中的某些生长因子。我们的发现提出了一种预防基于MSC的细胞疗法中移植细胞死亡的新策略。电子补充材料本文的在线版本(doi:10.1007 / s12192-013-0430-2)包含补充材料,授权用户可以使用。

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