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首页> 外文期刊>In vivo. >Influence of static magnetic fields combined with human insulin-like growth factor 1 on human satellite cell cultures.
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Influence of static magnetic fields combined with human insulin-like growth factor 1 on human satellite cell cultures.

机译:静磁场与人胰岛素样生长因子1结合对人卫星细胞培养的影响。

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摘要

Tissue engineering represents a promising research field, targeting the creation of new functional muscle tissue in vitro. The aim of the present study was to show the influence of static magnetic fields (SMF) and insulin-like growth factor-1 (IGF1), as enhancing stimuli on human satellite cell cultures, which are preferred sources of stem cells in engineering skeletal muscle tissue. To detect effects on myogenic maturation and proliferation, AlamarBlue? proliferation, assay and semi-quantitative reverse transcription-polymerase chain reaction of following markers was performed: desmin (DES), myogenic factor-5 (MYF5), myogenic differentiation antigen-1 (MYOD1), myogenin (MYOG), myosin heavy chain (MYH) and α1 actin (ACTA1). As a distinct marker of differentiation, immunohistochemical staining and fusion index determination was performed on satellite cell cultures stimulated with IGF1 and IGF1-plus-SMF with an intensity of 80 mT. Proliferation was increased by additional SMF application to IGF1-stimulated cell cultures on the first day of myogenesis. Relative gene expression of measured markers was increased by IGF1 application in the first days of myogenesis except for ACTA1. Additional SMF application enhanced this effect. Nevertheless we were unable to demonstrate the formation of contractile muscle tissue. Immunhistochemical staining verified muscle origin and all markers were displayed.
机译:组织工程代表了一个有前途的研究领域,其目标是在体外创建新的功能性肌肉组织。本研究的目的是显示静磁场(SMF)和胰岛素样生长因子1(IGF1)的影响,作为对人类卫星细胞培养物的刺激,后者是工程骨骼肌中干细胞的首选来源组织。为了检测对成肌成熟和增殖的影响,AlamarBlue?进行了以下标记的增殖,测定和半定量逆转录聚合酶链反应:结蛋白(DES),肌原因子5(MYF5),肌原分化抗原1(MYOD1),肌生成素(MYOG),肌球蛋白重链( MYH)和α1肌动蛋白(ACTA1)。作为分化的显着标志物,在强度为80 mT的IGF1和IGF1-plus-SMF刺激的卫星细胞培养物中进行了免疫组织化学染色和融合指数测定。在成肌的第一天,通过将SMF额外添加到IGF1刺激的细胞培养物中来增加增殖。除Acta1以外,在成肌的头几天,IGF1的应用增加了所测标记物的相对基因表达。其他SMF应用程序增强了这种效果。然而,我们无法证明收缩性肌肉组织的形成。免疫组织化学染色证实了肌肉起源,并显示了所有标志物。

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