April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Murine Epidermal Cells Can be Transdifferentiated Into Corneal Epithelial-Like Cells in the Corneal Epithelial Environment
Author Affiliations & Notes
  • A. Shiraishi
    Ophthalmology and Regenerative Medicine,
    Ehime Univ School of Medicine, Touon, Japan
  • T. Kobayashi
    Ophthalmology and Regenerative Medicine,
    Ehime Univ School of Medicine, Touon, Japan
  • Y. Hayshi
    Ophthalmology and Regenerative Medicine,
    Ehime Univ School of Medicine, Touon, Japan
  • Y. Ohashi
    Ophthalmology,
    Ehime Univ School of Medicine, Touon, Japan
  • Footnotes
    Commercial Relationships  A. Shiraishi, None; T. Kobayashi, None; Y. Hayshi, None; Y. Ohashi, None.
  • Footnotes
    Support  Grant-in-Aid for Scientific Research (C) 20592079 from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 357. doi:
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    • Get Citation

      A. Shiraishi, T. Kobayashi, Y. Hayshi, Y. Ohashi; Murine Epidermal Cells Can be Transdifferentiated Into Corneal Epithelial-Like Cells in the Corneal Epithelial Environment. Invest. Ophthalmol. Vis. Sci. 2010;51(13):357.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To investigate the potential for murine epidermal cell transdifferentiation into corneal epithelial-like cells.

Methods: : use epidermal cells (MKCs) were isolated from K12Cre/ZEG mice which expressed GFP (green fluorescent protein) induced by a cornea-specific keratin 12 gene. The MKCs were cultured in serum free medium (CnT-07). Equal numbers of MKCs and normal mouse corneal epithelial cells (MCEs) from wild type mice were mixed and seeded (1x104/cm2) onto plastic, an amniotic membrane (AM), or an epithelium-denuded WT mouse cornea. The cells were cultured in serum free medium (CnT-30) with 0.4 mM Ca or SHEM (5% FBS) for 4 days and examined for GFP expression by fluorescence microscopy.

Results: : GFP expression was detected in MKCs cultured on the epithelium-denuded mouse cornea with either CnT 30 or SHEM; however no GFP was detected in MKCs cultured on the plastic or AM. The GFP positive cells were predominantly detected in the corneal limbal region.

Conclusions: : The present study demonstrates that MKCs have the potential to transdifferentiate into corneal epithelial-like cells. The results indicate that transdifferentiation may require the effect of coculture with corneal epithelial cells, as well as the corneal limbal environment.

Keywords: cornea: epithelium • gene/expression • cornea: basic science 
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