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

机译:使用微图案法将人间充质干细胞的指向分化为软骨细胞

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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:通过使用内部和外部刺激诱导间充质干细胞(MSCs),可以获得软骨细胞的必要性。在该研究中,MSC被引导在改性的基材和L-抗坏血酸添加上进行分化。该研究的目的是通过使用几个不同的标记,将人体MSCs(HMSCs)直接通过定性和定量评估成为改性基质的软骨细胞。从脂肪组织(ACMSC)获得间充质干细胞。使用流式细胞术和多能量分析评价细胞茎。使用Parafilm开发了微型解放基板 通过机械方法,在获得扫描电子显微镜(SEM)图像和分析Imagej之后测量髓尺寸。将细胞接种在2.4×104个细胞/ ml中并孵育12天。通过在第6天和第12天使用Alcian蓝染色的免疫细胞化学方法和硫酸化胶原观察胶原II的表达。使用SEM成像观察细胞形态。 ADMSCS从脂肪组织中成功获得,并遵循间充质干细胞施。使用Parafilm良好地开发了微透明剂底物 并且可用于修改基材,因为ACMSCS仅在Pith(P)上未被Parafilm覆盖。 ADMSCS在观察中表达胶原蛋白II和GAG。细胞形态也证实,通过播种密度受到播种密度的影响,因为在更圆形的形状中发现了较圆形的粘合剂,并且在窄的佩蒂上表达了比宽粘性的更高的胶原II。

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