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Tissue-Specific Stem Cells
Article first published online: 5 JAN 2009
Copyright © 2008 AlphaMed Press
Volume 27, Issue 1, pages 165–174, January 2009
How to Cite
Takanaga, H., Tsuchida-Straeten, N., Nishide, K., Watanabe, A., Aburatani, H. and Kondo, T. (2009), Gli2 Is a Novel Regulator of Sox2 Expression in Telencephalic Neuroepithelial Cells. STEM CELLS, 27: 165–174. doi: 10.1634/stemcells.2008-0580
Author contributions: H.T.: conception and design, manuscript writing, collection, data analysis and interpretation; N.T.-S. and K.N.: data analysis and interpretation; A.W.: provision of study material; H.A.: financial support, provision of study material; T.K.: conception and design, financial support, data analysis and interpretation, manuscript writing, final approval of manuscript.
Disclosure of potential conflicts of interest is found at the end of this article.
First published online in STEM CELLSExpress October 16, 2008.
- Issue published online: 5 JAN 2009
- Article first published online: 5 JAN 2009
- Manuscript Accepted: 28 SEP 2008
- Manuscript Received: 18 JUN 2008
- Neural stem cells;
Multipotential neural stem cells (NSCs) in the central nervous system (CNS) proliferate indefinitely and give rise to neurons, astrocytes, and oligodendrocytes. As NSCs hold promise for CNS regeneration, it is important to understand how their proliferation and differentiation are controlled. We show here that the expression of sox2 gene, which is essential for the maintenance of NSCs, is regulated by the Gli2 transcription factor, a downstream mediator of sonic hedgehog (Shh) signaling: Gli2 binds to an enhancer that is vital for sox2 expression in telencephalic neuroepithelial (NE) cells, which consist of NSCs and neural precursor cells. Overexpression of a truncated form of Gli2 (Gli2ΔC) or Gli2-specific short hairpin RNA (Gli2 shRNA) in NE cells in vivo and in vitro inhibits cell proliferation and the expression of Sox2 and other NSC markers, including Hes1, Hes5, Notch1, CD133, and Bmi1. It also induces premature neuronal differentiation in the developing NE cells. In addition, we show evidence that Sox2 expression decreases significantly in the developing neuroepithelium of Gli2-deficient mice. Finally, we demonstrate that coexpression of Gli2ΔC and Sox2 can rescue the expression of Hes5 and prevent premature neuronal differentiation in NE cells but cannot rescue its proliferation. Thus these data reveal a novel transcriptional cascade, involving Gli2 Sox2 Hes5, which maintains the undifferentiated state of telencephalic NE cells. STEM CELLS2009;27:165–174