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使用脐带来源的生物支架基质进行人多能干细胞的无饲养层和无动物成分培养。

Feeder-free and xeno-free culture of human pluripotent stem cells using UCBS matrix.

作者信息

Ding Yan, Yang Hua, Yu Li, Xu Chang Long, Zeng Yi, Qiu Ying, Li Dong Sheng

机构信息

Hubei Key Laboratory of Embryonic Stem Cell Research, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, 442000, China.

Human Reproductive Medical Center of Nanning Second People's Hospital, The Third Affiliated Hospital of Guangxi Medical University, Nanning, 530031, China.

出版信息

Cell Biol Int. 2015 Oct;39(10):1111-9. doi: 10.1002/cbin.10484. Epub 2015 Jun 18.

Abstract

The ideal medium for human pluripotent stem cells (hPSCs) culture should be feeder-free, xeno-free, and completely defined. The present study aims to establish a new feeder-free and xeno-free system for culturing hPSCs. The system consists of the matrix, which was prepared from human umbilical cord blood serum (UCBS) and used to coat the culture plates, and the xeno-free medium, which was conventional serum-free hES medium supplemented with high concentrations of bFGF and Fibronectin. Compared with matrigel and mouse embryonic fibroblasts (MEFs), the UCBS matrix was proved to be equally suitable for the growth of hPSCs. After a series of experiments with different media and cytokins, the UCBS matrix was found worked the best with the basic medium (BM) supplemented with 20 ng/mL bFGF, 10 ug/mL fibronectin and Y-27632 for culture of hES cells. The hPSCs maintained normal karyotype, high proliferation rate and self-renewal ability after continuous culture more than 10 passages in this feeder-free and xeno-free system. Furthermore, a new human embryonic stem (hES) cell line was derived from discarded day 3 embryos in this newly developed culture system. In conclusion, this feeder-free and xeno-free system could not only be used to the culture hPSCs, but could also be used to derive new hES cell lines.

摘要

人类多能干细胞(hPSC)培养的理想培养基应无饲养层、无异源成分且完全明确。本研究旨在建立一种新的无饲养层和无异源成分的hPSC培养体系。该体系由基质和无异源成分的培养基组成,基质由人脐带血血清(UCBS)制备而成,用于包被培养板,无异源成分的培养基是在传统无血清hES培养基中添加高浓度的碱性成纤维细胞生长因子(bFGF)和纤连蛋白。与基质胶和小鼠胚胎成纤维细胞(MEF)相比,UCBS基质被证明同样适合hPSC的生长。在使用不同培养基和细胞因子进行一系列实验后,发现UCBS基质与添加20 ng/mL bFGF、10 μg/mL纤连蛋白和Y-27632的基础培养基(BM)配合用于hES细胞培养效果最佳。在这种无饲养层和无异源成分的体系中连续培养超过10代后,hPSC保持了正常的核型、高增殖率和自我更新能力。此外,在这个新开发的培养体系中,从废弃的第3天胚胎中获得了一株新的人类胚胎干细胞(hES)系。总之,这种无饲养层和无异源成分的体系不仅可用于hPSC的培养,还可用于获得新的hES细胞系。

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