Array analysis of the genes regulated during neuronal differentiation of human embryonal cells

被引:13
作者
Bani-Yaghoub, M
Felker, JM
Ozog, MA
Bechberger, JF
Naus, CCG [1 ]
机构
[1] Univ Western Ontario, Dept Anat & Cell Biol, London, ON N6A 5C1, Canada
[2] John P Robarts Res Inst, London, ON N6A 2K8, Canada
来源
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE | 2001年 / 79卷 / 04期
关键词
Atlas cDNA expression arrays; differentiation; neurodevelopment; neuron; NT2/D1; cells;
D O I
10.1139/bcb-79-4-387
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
Recent advances in genetic technology have provided a new platform on which the simultaneous analysis of a large number of genes is possible in a rapid and efficient fashion. To assess the differential expression of human genes during neuronal differentiation, we compared the transcript profiles of undifferentiated, partially differentiated, and fully differentiated NT2/D1 cultures with cDNA expression arrays. Approximately 75 genes (13% of the gene array pool) were differentially expressed during neuronal development of NT2/D1 cells. Genes coding for pyruvate kinase M2 isozyme, clathrin assembly proteins, calmodulin, fibronectin, laminin, thymosin beta-10, and many others were upregulated as NT2/D1 cells differentiated into neurons. In contrast, several kinases, phosphatases, and G-protein coupled receptor genes showed downregulation upon neuronal differentiation. The information provided here is an invaluable reference for characterizing the phenotype of these cells. This information can also be used in cell therapy and transplantation in which the graft microenvironment and interaction with the host tissue is crucial.
引用
收藏
页码:387 / 398
页数:12
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