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不同预处理方案对小鼠脂肪来源的基质/干细胞表达谱的影响。

Effect of Different Preconditioning Regimens on the Expression Profile of Murine Adipose-Derived Stromal/Stem Cells.

机构信息

Division of Nephrology, Department of Internal Medicine III, Goethe-University, 60596 Frankfurt/M., Germany.

Department of Biomedicine, Aarhus University, 8000 Aarhus, Denmark.

出版信息

Int J Mol Sci. 2018 Jun 10;19(6):1719. doi: 10.3390/ijms19061719.

Abstract

Stem cell-based therapies require cells with a maximum regenerative capacity in order to support regeneration after tissue injury and organ failure. Optimization of this regenerative potential of mesenchymal stromal/stem cells (MSC) or their conditioned medium by in vitro preconditioning regimens are considered to be a promising strategy to improve the release of regenerative factors. In the present study, MSC were isolated from inguinal adipose tissue (mASC) from C57BL/6 mice, cultured, and characterized. Then, mASC were either preconditioned by incubation in a hypoxic environment (0.5% O₂), or in normoxia in the presence of murine epidermal growth factor (EGF) or tumor necrosis factor α (TNFα) for 48 h. Protein expression was measured by a commercially available array. Selected factors were verified by PCR analysis. The expression of 83 out of 308 proteins (26.9%) assayed was found to be increased after preconditioning with TNFα, whereas the expression of 61 (19.8%) and 70 (22.7%) proteins was increased after incubation with EGF or in hypoxia, respectively. Furthermore, we showed the proliferation-promoting effects of the preconditioned culture supernatants on injured epithelial cells in vitro. Our findings indicate that each preconditioning regimen tested induced an individual expression profile with a wide variety of factors, including several growth factors and cytokines, and therefore may enhance the regenerative potential of mASC for cell-based therapies.

摘要

基于干细胞的疗法需要具有最大再生能力的细胞,以支持组织损伤和器官衰竭后的再生。通过体外预处理方案优化间充质基质/干细胞(MSC)或其条件培养基的这种再生潜能被认为是一种有前途的策略,可以提高再生因子的释放。在本研究中,从 C57BL/6 小鼠的腹股沟脂肪组织(mASC)中分离 MSC,进行培养和鉴定。然后,mASC 要么在低氧环境(0.5% O₂)中孵育,要么在常氧条件下在鼠表皮生长因子(EGF)或肿瘤坏死因子 α(TNFα)存在下孵育 48 小时。通过商业上可用的阵列测量蛋白质表达。通过 PCR 分析验证了选定的因子。在预处理 TNFα 后,检测到 308 种蛋白质中的 83 种(26.9%)的表达增加,而在孵育 EGF 或低氧条件下,分别有 61 种(19.8%)和 70 种(22.7%)蛋白质的表达增加。此外,我们还证明了预处理培养上清液对体外受损上皮细胞的促增殖作用。我们的研究结果表明,每种测试的预处理方案都诱导了具有广泛多种因子的个体表达谱,包括几种生长因子和细胞因子,因此可能增强 mASC 用于细胞治疗的再生潜能。

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