April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Human Epithelial Cell Cultures From Superficial Limbal Explants
Author Affiliations & Notes
  • Elena Basli
    Institut de la Vision UMR_S 968 -CNRS UMR_7210, Paris, France
    Service d'Ophtalmologie 5, CHNO des Quinze-Vingts, Paris, France
  • Djida Ghoubay-Benallaoua
    Institut de la Vision UMR_S 968 -CNRS UMR_7210, Paris, France
    Banque de Tissus, Etablissement Français du Sang- Ile-de-France, Paris, France
  • Pablo Goldschmidt
    Institut de la Vision UMR_S 968 -CNRS UMR_7210, Paris, France
    Laboratoire du CHNO des Quinze-Vingts, Paris, France
  • Florence Pecha
    Institut de la Vision UMR_S 968 -CNRS UMR_7210, Paris, France
    Banque de Tissus, Etablissement Français du Sang- Ile-de-France, Paris, France
  • Christine Chaumeil
    Laboratoire du CHNO des Quinze-Vingts, Paris, France
  • Laurent Laroche
    Institut de la Vision UMR_S 968 -CNRS UMR_7210, Paris, France
    Service d'Ophtalmologie 5, CHNO des Quinze-Vingts, Paris, France
  • Vincent Borderie
    Institut de la Vision UMR_S 968 -CNRS UMR_7210, Paris, France
    Banque de Tissus, Etablissement Français du Sang- Ile-de-France, Paris, France
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 5128. doi:
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      Elena Basli, Djida Ghoubay-Benallaoua, Pablo Goldschmidt, Florence Pecha, Christine Chaumeil, Laurent Laroche, Vincent Borderie; Human Epithelial Cell Cultures From Superficial Limbal Explants. Invest. Ophthalmol. Vis. Sci. 2011;52(14):5128.

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Abstract

Purpose: : To study the kinetics of growth and the phenotype of cells cultured from human limbal explants in a cholera toxin-free medium with no feeder cell layer.

Methods: : Human organ-cultured corneas were used to prepare limbal explants (full-thickness and superficial limbal explants). Cell growth kinetics and phenotypes were assessed by cultivating explants in cholera toxin-free Green medium. Morphological analysis was carried out twice a week with a phase contrast light microscope. Epithelial and progenitor cell markers were assessed by immunocytochemistry, flow cytometry, and RT-PCR.

Results: : The successful epithelial cell growth rates from full thickness limbal explant and superficial limbal explant tissues were 41 and 86%, respectively. The mean cell area and the percentage of small cells in superficial and full-thickness explant cultures were, respectively, 317 µm2 and 429 µm2, and 8.9% and 1.7%. The percentage of positive cells in superficial and full thickness limbal explant cultures as assessed by immunocytochemistry were the following: broad spectrum cytokeratins (MNF116), 82%/37%; CK3, 74%/25%; CK19, 46%/25%; vimentin, 56%/53%; delta N p63α, 54%/0%; and ABCG2, 5%/0%. Flow cytometry showed higher percentage of small cells, higher percentage of MNF116+ cells, and stronger expression of progenitor-associated markers in superficial than in full-thickness explant cultures. For superficial limbal explant cultures, the analysis of the expression profiles for various mRNAs at the end of 21 days of culture showed high levels of expression of the mRNAs encoding CK3, vimentin, and CK19. The expression of mRNA of delta N p63α and ABCG2 was weaker. Cultures obtained from full-thickness limbal explants featured no expression of mRNA of CK19, delta N p63α, and ABCG2, whereas mRNAs encoding CK3 and vimentin were detected.

Conclusions: : Superficial limbal explants appear to be superior to full thickness limbal explants for growing human limbal epithelial cells. Preparation of explants using surgical facilities (i.e., operating microscope and microsurgical blades) led to a dramatic increase in the percentage of successful cultures, higher epithelial cell growth, decreased fibroblast contamination, and better preservation of limbal epithelial progenitors.

Keywords: cornea: epithelium • immunohistochemistry • cell survival 
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