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Directed Differentiation of Human Mesenchymal Stem Cells into Chondrocytes Using Micropatterning Method

机译:使用微模式法将人间充质干细胞定向分化为软骨细胞

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The necessity of chondrocytes can be obtained by inducing Mesenchymal Stem Cells (MSCs) using internal and external stimuli. In this research, MSC was directed to be differentiated on modified substrate and L-ascorbic acid addition. The objective of this research is to direct human MSCs (hMSCs) to become chondrocytes on modified substrates by qualitative and quantitative evaluation using several spesific markers. Mesenchymal stem cells were obtained from adipose tissue (ADMSC). Cell stemness was evaluated using flow cytometry and multipotency analysis. Micropatterned substrate was developed using Parafilm by doing mechanical method and pith size was measured after getting Scanning Electron Microscope (SEM) image and analyzedusing imageJ. The cells were seeded in 2.4× 104 cells/mL and incubated for 12 days. The expression of Collagen II was observed by immunocytochemistry method and sulphated-GAG using Alcian Blue Staining on day 6 and day 12. Cell morphology was observed using SEM imaging. ADMSCs were successfully obtained from adipose tissue and complied the mesenchymal stem cellscriteria. The micropatterned substrate was well developed using Parafilm and could be used to modify the substrate because ADMSCs were only attached on pith (P) that was not covered by Parafilm. ADMSCs expressed Collagen II and GAG on day 6 and 12 of observation.The cells morphology also confirmed that chondrogenicdifferentiation was affected by seeding density because ADMSCs were found in more rounded shape and also expressed more Collagen II in narrow pith than in widepith.
机译:软骨细胞的必要性可以通过使用内部和外部刺激诱导间充质干细胞(MSC)来获得。在这项研究中,MSC旨在在修饰的底物和添加L-抗坏血酸的条件下进行分化。这项研究的目的是通过使用几种特殊的标记物进行定性和定量评估,指导人类MSC(hMSC)成为修饰基质上的软骨细胞。间充质干细胞获自脂肪组织(ADMSC)。使用流式细胞仪和多能性分析评估细胞干性。使用Parafilm开发了具有微图案的基材 通过机械方法,在获得扫描电子显微镜(SEM)图像并使用imageJ分析后,测量了髓的大小。将细胞以2.4×104细胞/ mL接种并孵育12天。通过免疫细胞化学方法观察胶原蛋白II的表达,并在第6天和第12天使用Alcian Blue Staining观察硫酸化GAG。从脂肪组织中成功获得了ADMSCs,并符合间充质干细胞标准。使用Parafilm可以很好地显影微图案化的基材 由于ADMSC仅附着在Parafilm未覆盖的髓(P)上,因此可用于修饰基质 。 ADMSC在观察的第6天和第12天表达胶原II和GAG。细胞形态也证实了成软骨分化受接种密度的影响,因为ADMSC呈更圆的形状,并且在窄髓中表达的胶原II比在宽处表达的更多。

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