首页> 外文期刊>Journal of biomedical materials research, Part A >The effect of temporal manipulation of transforming growth factor beta 3 and fibroblast growth factor 2 on the derivation of proliferative chondrocytes from mensenchymal stem cells—A study monitored by quantitative reverse transcription polymerase chain reaction and molecular beacon based nanosensors
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The effect of temporal manipulation of transforming growth factor beta 3 and fibroblast growth factor 2 on the derivation of proliferative chondrocytes from mensenchymal stem cells—A study monitored by quantitative reverse transcription polymerase chain reaction and molecular beacon based nanosensors

机译:转化生长因子β3和成纤维细胞生长因子2的时间操纵对纯敏性干细胞增殖软骨细胞的衍生衍生 - 通过定量逆转录聚合酶链反应和分子信标基纳米调传料检测的研究

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Abstract Proliferative chondrocytes are critical to realize regeneration of damaged epiphyseal growth plate. However, acquiring autologous replacement cells involves highly invasive procedures and often results in limited cell quantity. Mesenchymal stem cells (MSCs) are a potential source of chondrogenic cells for the treatment of cartilage disorders and injuries. The temporal effect of transforming growth factor beta 3 (TGFβ3) and fibroblast growth factor 2 (FGF2) on the derivation of proliferative chondrocytes from MSCs in three‐dimensional agarose was investigated by manipulating the duration of TGFβ3 and FGF2 treatment. The differentiation process was monitored by quantitative reverse transcription polymerase chain reaction (qRT‐PCR) as well as nanosensors containing two molecular beacons that target critical biomarkers for proliferative chondrocytes (i.e., collagen type‐II messenger ribonucleic acid [mRNA] and Ki67 mRNA). The molecular beacon‐based nanosensors were found to be comparable to qRT‐PCR in measuring mRNA expression and thus providing a noninvasive mean to screen and monitor culture samples. ? 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 895–904, 2018.
机译:摘要增殖性软骨细胞对于实现受损骨骺生长板的再生至关重要。然而,获取自体替代细胞涉及高度侵入性的程序,并且经常导致细胞量有限。间充质干细胞(MSCs)是用于治疗软骨障碍和伤害的软骨内细胞的潜在来源。通过操纵TGFβ3和FGF2处理来研究转化生长因子β3(TGFβ3)和成纤维细胞生长因子2(FGF2)对来自三维琼脂糖的MSC的增殖软骨细胞的衍生的时间效应。通过定量逆转录聚合酶链反应(QRT-PCR)和纳米传感器监测分化过程,以及含有两个分子信标的纳米传感器,其针对增殖软骨细胞的关键生物标志物(即,胶原蛋白-II代理核糖核酸[mRNA]和KI67 mRNA)。发现基于分子信标的纳米传感器与测量mRNA表达中的QRT-PCR相当,因此提供非侵入性的平均值筛选和监测培养样品。还2017年Wiley期刊,Inc。J生物保罗第A部分:106A:895-904,2018。

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