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Spatial and temporal regulation of Wnt/beta-catenin signaling is essential for development of the retinal pigment epithelium

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    SYSNO ASEP0334091
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleSpatial and temporal regulation of Wnt/beta-catenin signaling is essential for development of the retinal pigment epithelium
    Author(s) Fujimura, Naoko (UMG-J)
    Taketo, M.M. (JP)
    Mori, M. (JP)
    Kořínek, Vladimír (UMG-J) RID
    Kozmik, Zbyněk (UMG-J) RID
    Number of authors5
    Source TitleDevelopmental Biology. - : Elsevier - ISSN 0012-1606
    Roč. 334, č. 1 (2009), s. 31-45
    Number of pages15 s.
    Languageeng - English
    CountryUS - United States
    Keywordseye ; Wnt ; retina ; pigment
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsGA204/08/1618 GA ČR - Czech Science Foundation (CSF)
    1M0520 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    2B06077 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z50520514 - UMG-J (2005-2011)
    UT WOS000272260600004
    DOI10.1016/j.ydbio.2009.07.002
    AnnotationWnt/beta-catenin signaling is highly active in the dorsal retinal pigment epithelium (RPE) during eye development. To study the role of Wnt/beta-catenin signaling in the RPE development we used a conditional Cre/loxP system in mice to inactivate or ectopically activate Wnt/beta-catenin signaling in the RPE. Inactivation of Wnt/beta-catenin signaling results in transdifferentiation of RPE to neural retina (NR) as documented by downregulation of RPE-specific markers Mitf and Otx2 and ectopic expression of NR-specific markers Chx10 and Rx, respectively. In contrast, ectopic activation of Wnt/beta-catenin signaling results in the disruption of the RPE patterning, indicating that precise spatial and temporal regulation of Wnt/beta-catenin signaling is required for normal RPE development. Combined, our data suggest that Wnt/beta-catenin signaling plays an essential role in development of RPE by maintaining or inducing expression of Mitf and Otx2.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2010
Number of the records: 1  

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