A directional Wnt/β-catenin-Sox2-proneural pathway regulates the transition from proliferation to differentiation in the Xenopus retina

被引:92
作者
Agathocleous, Michalis [2 ]
Iordanova, Ilina [2 ]
Willardsen, Minde I. [1 ]
Xue, Xiao Yan [2 ]
Vetter, Monica L. [1 ]
Harris, William A. [2 ]
Moore, Kathryn B. [1 ]
机构
[1] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT 84132 USA
[2] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3DY, England
来源
DEVELOPMENT | 2009年 / 136卷 / 19期
基金
英国惠康基金;
关键词
Sox; Neuron; Progenitor; Proneural; Retina; Wnt; Xenopus; CELL-FATE DETERMINATION; WNT SIGNALING PATHWAY; BHLH FACTORS XATH5; BETA-CATENIN; PRIMARY NEUROGENESIS; PROGENITOR CELLS; STEM-CELLS; MOLECULAR CHARACTERIZATION; DEVELOPMENTAL EXPRESSION; TRANSCRIPTION FACTORS;
D O I
10.1242/dev.040451
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Progenitor cells in the central nervous system must leave the cell cycle to become neurons and glia, but the signals that coordinate this transition remain largely unknown. We previously found that Wnt signaling, acting through Sox2, promotes neural competence in the Xenopus retina by activating proneural gene expression. We now report that Wnt and Sox2 inhibit neural differentiation through Notch activation. Independently of Sox2, Wnt stimulates retinal progenitor proliferation and this, when combined with the block on differentiation, maintains retinal progenitor fates. Feedback inhibition by Sox2 on Wnt signaling and by the proneural transcription factors on Sox2 mean that each element of the core pathway activates the next element and inhibits the previous one, providing a directional network that ensures retinal cells make the transition from progenitors to neurons and glia.
引用
收藏
页码:3289 / 3299
页数:11
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