Characterization of glycoconjugate antigens in mouse embryonic neural precursor cells

被引:54
作者
Yanagisawa, M
Taga, T
Nakamura, K
Ariga, T
Yu, RK
机构
[1] Med Coll Georgia, Inst Mol Med & Genet, Augusta, GA 30912 USA
[2] Kumamoto Univ, 21 Century COE Program, Cell Fate Regulat Res & Educ Unit, Kumatori, Osaka, Japan
[3] Kumamoto Univ, Dept Cell Fate Modulat, Inst Mol Embryol & Genet, Kumamoto, Japan
[4] Kitasato Univ, Sch Med, Dept Biochem, Kanagawa, Japan
关键词
glycolipids; glycoproteins; integrin; neural development; neuroepithelial cells;
D O I
10.1111/j.1471-4159.2005.03452.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neuronal and glial cells organizing the central nervous system (CNS) are generated from common neural precursor cells (NPCs) during neural development. However, the expression of cell-surface glycoconjugates that are crucial for determining the properties and biological function of these cells at different stages of development has not been clearly defined. In this study, we investigated the expression of several stage-specific glycoconjugate antigens, including several b-series gangliosides GD3, 9-O-acetyl GD3, GT1b and GQ1b, stage-specific embryonic antigen-1 (SSEA-1) and HNK-1, in mouse embryonic NPCs employing immunocytochemistry and flow cytometry. In addition, several of these antigens were positively identified by chemical means for the first time. We further showed that the SSEA-1 immunoreactivity was contributed by both glycoprotein and glycolipid antigens, and that of HNK-1 was contributed only by glycoproteins. Functionally, SSEA-1 may participate in migration of the cells from neurospheres in an NPC cell culture system, and the effect could be repressed by anti-SSEA-1 antibody. Based on this observation, we identified beta 1 integrin as one of the SSEA-1 carrier glycoproteins. Our data thus provide insights into the functional role of certain glycoconjugate antigens in NPCs during neural development.
引用
收藏
页码:1311 / 1320
页数:10
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