Role of integrins in differentiation of chick retinal pigmented epithelial cells in vitro

Authors

  • Yuichi Mazaki,

    Corresponding author
    1. Division of Morphogenesis, Department of Developmental Biology, National Institute for Basic Biology and Department of Molecular Biomechanics, School of Life Science, The Graduate University for Advanced Studies, Okazaki, 444 Japan.
      * Author to whom all correspondence should be addressed at: Division of Morphogenesis, Department of Developmental Biology, National Institute for Basic Biology, Myodaiji-chou 38, Okazaki, Aichi, 444 Japan.
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  • Makoto Mochii,

    1. Division of Morphogenesis, Department of Developmental Biology, National Institute for Basic Biology and Department of Molecular Biomechanics, School of Life Science, The Graduate University for Advanced Studies, Okazaki, 444 Japan.
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  • Ryuji Kodama,

    1. Division of Morphogenesis, Department of Developmental Biology, National Institute for Basic Biology and Department of Molecular Biomechanics, School of Life Science, The Graduate University for Advanced Studies, Okazaki, 444 Japan.
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  • Goro Eguchi

    1. Division of Morphogenesis, Department of Developmental Biology, National Institute for Basic Biology and Department of Molecular Biomechanics, School of Life Science, The Graduate University for Advanced Studies, Okazaki, 444 Japan.
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* Author to whom all correspondence should be addressed at: Division of Morphogenesis, Department of Developmental Biology, National Institute for Basic Biology, Myodaiji-chou 38, Okazaki, Aichi, 444 Japan.

Abstract

When retinal pigmented epithelial cells (PEC) of chick embryos are cultured under appropriate conditions, the phenotype changes to that of lens cells through a process known as transdifferentiation. The first half of the process, characterized by dedifferentiation of PEC, is accompanied by a marked decrease in adhesiveness of PEC to collagen type I- or type IV-coated dishes. To understand the underlying mechanisms of this change, we analyzed the expression of integrins, which are major receptors for extracellular matrix components. Northern blot analysis with cDNA probes for chicken α3, α6, α8, αv, β1 and β5 integrin mRNA showed that the genes for all these integrins are transcribed at similar levels in PEC and dedifferentiated PEC (dePEC). Further analysis of β1 integrin, which is a major component of integrin heterodimers, showed that although the protein amount of β1 integrin was not changed, its localization at focal contacts seen in PEC was lost in dePEC. When anti-β1 integrin antibody was added to the PEC culture medium, a decrease of cell-substrate adhesiveness occurred, followed by a gradual change in both morphology and gene expression patterns to ones similar to those of dePEC. These findings suggest that an appropriate distribution of β1 integrin plays an essential role in maintaining the differentiated state of PEC through cell-substrate adhesion.

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