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

被引:9
|
作者
Ding, Yan [1 ]
Yang, Hua [2 ]
Yu, Li [1 ]
Xu, Chang Long [2 ]
Zeng, Yi [3 ]
Qiu, Ying [2 ]
Li, Dong Sheng [1 ]
机构
[1] Hubei Univ Med, Taihe Hosp, Hubei Key Lab Embryon Stem Cell Res, Shiyan 442000, Hubei, Peoples R China
[2] Guangxi Med Univ, Human Reprod Med Ctr, Nanning Peoples Hosp 2, Affiliated Hosp 3, Nanning 530031, Peoples R China
[3] Beijing Univ Ind, Coll Life Sci & Bioengn, Beijing 100124, Peoples R China
关键词
human pluripotent stem cells; ROCK inhibitor; umbilical cord blood serum; CORD BLOOD-SERUM; EPIDERMAL-GROWTH-FACTOR; DIFFERENTIATION; PROLIFERATION; EXPANSION; THERAPY;
D O I
10.1002/cbin.10484
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:1111 / 1119
页数:9
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