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

机译:通过人类脂肪来源的间充质干细胞的分化过氧化氢诱导的DNA损伤和修复

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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 μM 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:人类脂肪来源的间充质干细胞(hADMSC)被认为是细胞组织治疗中的潜在工具,因为它们具有在体外增殖和分化的能力。已有几项研究探讨了它们在再生医学中的应用。然而,关于它们对DNA损伤,特别是对植入的微环境中存在的活性氧(ROS)的反应知之甚少。在这项研究中,我们使用了ROS诱导剂过氧化氢来探索(1)hADMSC和(2)衍生的终末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hADMSCs暴露于过氧化氢后,DNA断裂和氧化性损伤(甲酰嘧啶DNA糖基化酶敏感位点)的剂量均增加。在暴露于150和200μm过氧化氢的细胞中,hADMSC的DNA修复能力受到影响。通过脂肪细胞分化观察到DNA断裂和氧化性DNA损伤的基础水平增加。此外,过氧化氢诱导的DNA损伤通过脂肪细胞的分化而增加。 DNA修复能力也下降。这项研究是成脂分化过程中DNA修复能力的第一份后续报告。值得注意的是,在终末分化的脂肪细胞中,DNA断裂修复被取消,而DNA氧化损伤的修复仍然有效。

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