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Hydrogen Peroxide-Induced DNA Damage and Repair through the Differentiation of Human Adipose-Derived Mesenchymal Stem Cells

机译:过氧化氢诱导的DNA损伤和通过分化的人脂肪衍生的间充质干细胞进行修复

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摘要

Human adipose-derived mesenchymal stem cells (hADMSCs) are recognized as a potential tool in cell tissue therapy because of their capacity to proliferate and differentiate in vitro. Several studies have addressed their use in regenerative medicine; however, little is known regarding their response to DNA damage and in particular to the reactive oxygen species (ROS) that are present in the microenvironment of implantation. In this study, we used the ROS-inducing agent hydrogen peroxide to explore the responses of (1) hADMSCs and (2) derived terminally differentiated adipocytes to oxidatively generated DNA damage. Using single cell gel electrophoresis, a dose-related increase was found for both DNA breaks and oxidative lesions (formamidopyrimidine DNA glycosylase-sensitive sites) upon exposure of hADMSCs to hydrogen peroxide. DNA repair capacity of hADMSCs was affected in cells exposed to 150 and 200 mu M of hydrogen peroxide. An increase in the basal levels of DNA breaks and oxidative DNA lesions was observed through adipocyte differentiation. In addition, hydrogen peroxide-induced DNA damage increased through adipocyte differentiation; DNA repair capacity also decreased. This study is the first follow-up report on DNA repair capacity during adipogenic differentiation. Remarkably, in terminally differentiated adipocytes, DNA breakage repair is abolished while the repair of DNA oxidative lesions remains efficient.
机译:人脂肪衍生的间充质干细胞(HADMSCs)被认为是细胞组织治疗中的潜在工具,因为它们在体外增殖和分化的能力。几项研究已经解决了他们在再生医学中使用;然而,关于它们对DNA损伤的反应很少,特别是植入中的微环境中存在的反应性氧物质(ROS)。在该研究中,我们使用过氧化芳烃诱导剂氢过氧化氢以探讨(1)哈米乳蛋白酶和(2)衍生的末端分化的脂肪细胞对氧化产生的DNA损伤的反应。使用单细胞凝胶电泳,发现对DNA断裂和氧化病变(甲状腺嘧啶DNA糖基糖基糖基糖基酶敏感位点)发现与过氧化氢的氧化病变(甲状腺嘧啶DNA糖基糖基糖基糖酶敏感位点)进行了与剂量相关的升高。 HADMSCs的DNA修复能力在暴露于150-200μm的细胞中受到过氧化氢的细胞。通过adipyyte分化观察到DNA断裂和氧化DNA病变的基础水平的增加。此外,通过脂肪细胞分化增加过氧化氢诱导的DNA损伤; DNA修复能力也降低。本研究是脂肪分化期间DNA修复能力的第一次随访报告。值得注意的是,在终末分化的脂肪细胞中,在DNA氧化病变的修复保持效率的同时废除DNA破碎修复。

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