In vitro characterization of a human neural progenitor cell coexpressing SSEA4 and CD133

被引:72
作者
Barraud, Perrine
Stott, Simon
Mollgard, Kjeld
Parmar, Malin
Bjorklund, Anders
机构
[1] Lund Univ, Res Ctr Stem Cell Biol & Cell Therapy, Lund, Sweden
[2] Univ Copenhagen, Panum Inst, DK-2200 Copenhagen, Denmark
关键词
forebrain; flow cytometry; neurosphere; sphere-forming assay;
D O I
10.1002/jnr.21116
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The stage-specific embryonic antigen 4 (SSEA4) is commonly used as a cell surface marker to identify the pluripotent human embryonic stem (ES) cells. Immunohistochemistry on human embryonic central nervous system revealed that SSEA4 is detectable in the early neuroepithelium, and its expression decreases as development proceeds. Flow cytometry analysis of forebrain-derived cells demonstrated that the SSEA4-expressing cells are enriched in the neural stem/progenitor cell fraction (CD133(+)), but are rarely cocletected with the neural stem cell (NSC) marker CD15. Using a sphere-forming assay, we showed that both subfractions CD133'/SSEA4+ and CD133(+)/CD15(+) isolated from the embryonic forebrain are enriched in neurosphere-initiating cells. In addition CD133, SSEA4, and CD15 expression is sustained in the expanded neurosphere cells and also mark subfractions of neurosphere-initiating cells. Therefore, we propose that SSEA4 associated with CD133 can be used for both the positive selection and the enrichment of neural stem/progenitor cells from human embryonic forebrain. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:250 / 259
页数:10
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