首页> 外文期刊>Progress in Artificial Intelligence >Up-Regulation of Superoxide Dismutase 2 in 3D Spheroid Formation Promotes Therapeutic Potency of Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells
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Up-Regulation of Superoxide Dismutase 2 in 3D Spheroid Formation Promotes Therapeutic Potency of Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells

机译:3D球状形成中超氧化物歧化酶2的上调促进人脐带血液源性间充质干细胞的治疗效力

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摘要

Umbilical cord blood-derived mesenchymal stem cells (UCB-MSCs) are accessible, available in abundance, and have been shown to be a promising source that can regenerate cartilage in patients with osteoarthritis or other orthopedic diseases. Recently, a three-dimensional (3D) cell culture system was developed to mimic the naive tissue microenvironment. However, the efficacy of cells generated from the 3D spheroid culture system has not yet been elucidated. In the present study, we demonstrate the changes in superoxide dismutase 2 (SOD2) gene expression, an indicator of oxidative stress, on 3D spheroid MSCs. Moreover, siRNA transfection and neutralizing antibody investigations were performed to confirm the function of SOD2 and E-cadherin. Overall, we found that SOD2 siRNA transfection in the spheroid form of MSCs increases the expression of apoptotic genes and decreases the clearance of mitochondrial reactive oxygen species (ROS). As a result, we confirm that 3D spheroid formation increases E-cadherin and SOD2 expression, ultimately regulating the phosphoinositide 3-kinase (PI3K/pAkt/pNrf2 and pERK/pNrf2 signaling pathway. Additionally, we show that SOD2 expression on 3D spheroid MSCs affects the regeneration rates of destructive cartilage in an osteoarthritic model. We postulate that the impact of SOD2 expression on 3D spheroid MSCs reduces oxidative stress and apoptosis, and also promotes cartilage regeneration.
机译:脐带血液衍生的间充质干细胞(UCB-MSCs)可获得丰富,并且已被证明是一种有前途的来源,可在骨关节炎或其他整形外疾病中再生软骨。最近,开发了一种三维(3D)细胞培养系统以模仿幼稚的组织微环境。然而,从3D球体培养系统产生的细胞的功效尚未阐明。在本研究中,我们证明了在3D球体MSC上的超氧化物歧化酶2(SOD2)基因表达,氧化应激指示剂的变化。此外,进行SiRNA转染和中和抗体研究以确认SOD2和E-CDADHERIN的功能。总体而言,我们发现MSCs的球状体形式的SOD2 siRNA转染增加了凋亡基因的表达,并降低了线粒体反应性氧物质(ROS)的间隙。结果,我们确认3D球状形成增加了E-Cadherin和SOD2表达,最终调节磷酸膦酸3-激酶(PI3K / PAKT / PNRF2和PERK / PNRF2信号通路。另外,我们表明SOD2表达3D Spheroid MSCs影响骨关节炎模型中破坏性软骨的再生率。假设SOD2表达对3D球体MSCs的影响减少了氧化应激和凋亡,并促进了软骨再生。

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