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Negative regulatory effect of an oligodendrocytic bHLH factor OLIG2 on the astrocytic differentiation pathway
被引:82
作者:
Fukuda, S
Kondo, T
Takebayashi, H
Taga, T
[1
]
机构:
[1] Kumamoto Univ, Dept Cell Fate Modulat, Inst Mol Embryol & Genet, Kumamoto 8600811, Japan
[2] Kumamoto Univ, 21st Century COE Program Cell Fate Regulat Res &, Kumamoto 8600811, Japan
[3] Natl Inst Physiol Sci, Div Mol Neurobiol, Okazaki, Aichi 4448585, Japan
关键词:
OLIG2;
p300;
STAT3;
cytokine;
neuroepithelial cell;
astrocytic differentiation;
D O I:
10.1038/sj.cdd.4401332
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:
In the developing vertebrate nervous system, multipotent neural stem cells produce both neurons and glia. OLIG2 is a basic helix-loop-helix transcription factor that plays critical roles in oligodendrocyte and motor neuron development; however, its role in astrocytic development remains elusive. In this study, we analyzed an effect of OLIG2 on cytokine-induced astrocytic differentiation from mouse telencephalic neuroepithelial cells. We show that the presence of OLIG2 protein leads to inhibition of the promoter activation of astrocyte-specific glial fibrillary acidic protein gene. We found that OLIG2 abolishes complex formation between a transcriptional coactivator p300 and a transcription factor, signal transducer and activator of transcription 3 (STAT3), which is activated by astrocytic differentiation-inducing cytokines, such as leukemia inhibitory factor (LIF). The enforced expression of OLIG2 in neuroepithelial cells inhibits the LIF-induced astrocytic differentiation. We also show that the OLIG2 protein in the nuclei of neural precursor cells disappears in accordance with astrocytic differentiation during culture with LIF. Together, these results reveal a novel molecular function of OLIG2 on the astrocyte development.
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页码:196 / 202
页数:7
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