Source:http://linkedlifedata.com/resource/pubmed/id/21354309
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2011-3-29
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pubmed:abstractText |
Wnt signaling is important in development and carcinogenesis. We previously showed that active ?-catenin or Lef-1 in the mammalian retinal culture prevents differentiation of retinal cells without modifying cellular proliferation. In this study, we investigated the in vivo role of ?-catenin in mouse retinal differentiation in transgenic mice, in which retinal-specific activation or inactivation of ?-catenin was achieved with Cre recombinase. The gain-of-function mice exhibited small eyes and large cell aggregates consisting of early progenitor cells labeled with SSEA-1 in the peripheral retina. In the loss-of-function mice, we observed a reduced number of SSEA-1-positive progenitor cells and the presence of differentiated cells in the ?-catenin ablated retinal region. Interestingly, the number of proliferating cells in the ?-catenin gain-of-function mice was highly downregulated, and the proliferation index detected by Ki67 expression was slightly lower than that of control mice in the ?-catenin loss-of-function mice. The Gsk-3? inhibitor BIO induced expression of Id3, which was highly expressed in SSEA-1-positive cells, and transiently maintained SSEA-1-positive retinal progenitor cells (RPCs). Forced expression of Id3 in RPCs mimicked the effects of BIO. Taken together, ?-catenin signaling regulates the timing of differentiation in RPCs by inhibiting premature differentiation of them partly through the regulation of Id3 expression.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD15,
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/Idb3 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Inhibitor of Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/Wnt Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/beta Catenin
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1095-9327
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
46
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
770-80
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pubmed:meshHeading |
pubmed-meshheading:21354309-Animals,
pubmed-meshheading:21354309-Antigens, CD15,
pubmed-meshheading:21354309-Biological Markers,
pubmed-meshheading:21354309-Cell Differentiation,
pubmed-meshheading:21354309-Cells, Cultured,
pubmed-meshheading:21354309-Inhibitor of Differentiation Proteins,
pubmed-meshheading:21354309-Mice,
pubmed-meshheading:21354309-Mice, Inbred C57BL,
pubmed-meshheading:21354309-Promoter Regions, Genetic,
pubmed-meshheading:21354309-Retina,
pubmed-meshheading:21354309-Signal Transduction,
pubmed-meshheading:21354309-Stem Cells,
pubmed-meshheading:21354309-Wnt Proteins,
pubmed-meshheading:21354309-beta Catenin
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pubmed:year |
2011
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pubmed:articleTitle |
?-Catenin signaling regulates the timing of cell differentiation in mouse retinal progenitor cells.
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pubmed:affiliation |
Department of Molecular and Developmental Biology, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, 108-8639 Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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