Differentiation of human oligodendrocytes from pluripotent stem cells

被引:191
作者
Hu, Bao-Yang [1 ]
Du, Zhong-Wei [1 ]
Zhang, Su-Chun [1 ]
机构
[1] Univ Wisconsin, Waisman Ctr, Dept Anat & Neurol,Sch Med & Publ Hlth, WiCell Inst, Madison, WI 53705 USA
关键词
CENTRAL-NERVOUS-SYSTEM; TRANSCRIPTION FACTORS; PROGENITOR CELLS; MOTOR-NEURONS; SPINAL-CORD; IN-VITRO; SPECIFICATION; OLIG2; GENERATION; NKX2.2;
D O I
10.1038/nprot.2009.186
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a four-part protocol to differentiate human embryonic stem cells (hESCESCESCs) to oligodendrocyte progenitor cells (OPCOPCOPCs) according to developmental principles. In the first 2 weeks, hESCESCESCs are induced to differentiate into neuroepithelial cells, which form neural tube-like rosettes. In the following 10 d, these neuroepithelial cells are specified to OLOLIG2-expressing progenitors in the presence of retinoic acid (RARA) and sonic hedgehog (SHH). Upon treatment with fibroblast growth factor 2 (FGF2) for another 10 d, these progenitors convert to OLOLIG2 and NKX2.2-expressing pre-OPCOPCOPCs. Finally, the pre-OPCOPCOPCs take 8-9 weeks to differentiate into OPCOPCOPCs, which express additional markers of oligodendrocytes, such as SOSOX10, platelet-derived growth factor receptor alpha (PDGFR alpha) and NG2. The unique aspects of the protocol are the use of FGF2 to promote the differentiation of gliogenic pre-OPCOPCOPCs in the third part and the removal of FGF2 during the transition of pre-OPCOPCOPCs to OPCOPCOPCs. This 3-month differentiation protocol consistently yields OPCOPCOPCs of high purity capable of producing myelin sheaths in vivo.
引用
收藏
页码:1614 / 1622
页数:9
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