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First published online 18 May 2005
doi: 10.1242/dev.01856
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1 RIKEN Center for Developmental Biology, 2-2-3 Minatojima Minamimachi, Chuo-ku,
Kobe 650-0047, Japan
2 Department of Cell and Developmental Biology, Graduate School of Biostudies,
Kyoto University, Kitashirakawa, Sakyo-ku, Kyoto 606-8502, Japan
Author for correspondence (e-mail:
nakagawas{at}riken.jp)
Accepted 7 April 2005
During the development of the central nervous system, cell proliferation and differentiation are precisely regulated. In the vertebrate eye, progenitor cells located in the marginal-most region of the neural retina continue to proliferate for a much longer period compared to the ones in the central retina, thus showing stem-cell-like properties. Wnt2b is expressed in the anterior rim of the optic vesicles, and has been shown to control differentiation of the progenitor cells in the marginal retina. In this paper, we show that stable overexpression of Wnt2b in retinal explants inhibited cellular differentiation and induced continuous growth of the tissue. Notably, Wnt2b maintained the undifferentiated progenitor cells in the explants even under the conditions where Notch signaling was blocked. Wnt2b downregulated the expression of multiple proneural bHLH genes as well as Notch. In addition, expression of Cath5 under the control of an exogenous promoter suppressed the negative effect of Wnt2b on neuronal differentiation. Importantly, Wnt2b inhibited neuronal differentiation independently of cell cycle progression. We propose that Wnt2b maintains the naive state of marginal progenitor cells by attenuating the expression of both proneural and neurogenic genes, thus preventing those cells from launching out into the differentiation cascade regulated by proneural genes and Notch.
Key words: Wnt, retina, progenitor cells, stem cells, proneural gene, Notch, Delta, differentiation, cell cycle
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