小鼠胚胎成纤维细胞生物支架维持小鼠胚胎干细胞的多能性

Rifqah Mifthahul Jannah, A. Naroeni, T. Novianti
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引用次数: 0

摘要

使用合成或生物材料开发了各种细胞培养策略;大多数现有出版物使用许多试剂。小鼠胚胎成纤维细胞(MEF)生物支架增强细胞附着、相互作用和生长因子的产生。由于生物支架可以维持和刺激干细胞的多能性,我们进行了这项研究来证明生物支架的功能。将MEF培养在DMEM完全培养基中,添加硫酸葡聚糖和l -抗坏血酸,以增加细胞外基质的生成,制备生物支架。该培养基作为胚胎干细胞(ESC)培养基。我们使用tali细胞仪根据Sox2和Oct4蛋白这两种干细胞标记物对干细胞进行鉴定和定量。与MEF培养相比,使用生物支架培养的ESC保持了ESC的多能性,这表明Oct 4和Sox2作为ESC标记存在。通过本研究,可以开发MEF生物支架作为ESC的培养基,以提高其繁殖能力。此外,它是组织工程和体外器官发育的模型。
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BIOSCAFFOLD FROM MOUSE EMBRYONIC FIBROBLAST MAINTAINS THE PLURIPOTENCY OF MOUSE EMBRYONIC STEM CELLS
Cell culture using a 3D method provides Various cell culture strategies have been developed using synthetic or biological materials; most existing publications use many reagents. Bioscaffold from mouse embryonic fibroblast (MEF) enhances cell attachment, interaction, and production of growth factors. Since bioscaffolds could maintain and stimulate pluripotency of stem cells, we conducted this study to prove bioscaffold function. Bioscaffold was prepared from MEF cultured in  DMEM complete medium supplemented with dextran sulfate and L-ascorbic acid to increase extracellular matrix production. This medium acts as an embryo stem cell (ESC) culture medium. We used a Tali-cytometer to identify and quantify stem cells based on Sox2 and Oct4 proteins, markers of stemness. ESC culture using bioscaffold maintained the pluripotency of ESC as indicated by the presence of  Oct 4 and Sox2 as ESC markers compared to MEF culture. From this research, the bioscaffold from MEF can be developed as media for ESC to improve propagation. Furthermore, it is a model for tissue engineering and in vitro organ development.
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