April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Expression of Pluripotency/Multipotency Markers in Human Corneal, Limbal and Cultivated Limbal Epithelium
Author Affiliations & Notes
  • M. Pauklin
    Department of Ophthalmology, University of Duisburg-Essen, Essen, Germany
    Department of General and Molecular Pathology, University of Tartu, Tartu, Estonia
  • H. Thomasen
    Department of Ophthalmology, University of Duisburg-Essen, Essen, Germany
  • S. Brockmann-Ahmed
    Department of Ophthalmology, University of Duisburg-Essen, Essen, Germany
  • K.-P. Steuhl
    Department of Ophthalmology, University of Duisburg-Essen, Essen, Germany
  • D. Meller
    Department of Ophthalmology, University of Duisburg-Essen, Essen, Germany
  • Footnotes
    Commercial Relationships  M. Pauklin, None; H. Thomasen, None; S. Brockmann-Ahmed, None; K.-P. Steuhl, None; D. Meller, None.
  • Footnotes
    Support  Estonian Scientific Foundation (grant no. 5832); German Society of Ophthalmology (DOG); Deutsche Forschungsgemeinschaft (DFG, Bonn, ME 1623/3-1)
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 1775. doi:
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    • Get Citation

      M. Pauklin, H. Thomasen, S. Brockmann-Ahmed, K.-P. Steuhl, D. Meller; Expression of Pluripotency/Multipotency Markers in Human Corneal, Limbal and Cultivated Limbal Epithelium. Invest. Ophthalmol. Vis. Sci. 2009;50(13):1775.

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

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Abstract

Purpose: : Corneal epithelial stem cells (SC) are located in the limbal zone. Recent studies have shown that several adult stem cells express pluripotency markers and can under certain conditions differentiate into a wide range of cell types.The objective of this study was to analyze the expression of key molecules needed for the maintenance of pluripotency in the human corneal and limbal epithelium, as well as in cultivated limbal epithelium.

Methods: : Four samples of human corneal, limbal and on intact amniotic membrane cultivated limbal epithelium were analyzed. The expression of corneal epithelial differentiation markers (K3, K12, K15 and Cx43), putative limbal SC markers (ABCG2, p63), and molecules expressed in pluripotent/multipotent SCs (NANOG, OCT4 (POU5F1), SOX2, KLF4, KIT, NESTIN, PAX6) was examined using Real-Time PCR.

Results: : The expression of all studied markers was detected in all samples of limbal and corneal epithelium. Limbal epithelium showed a significantly (p<0.05) higher expression of K15, ABCG2, OCT4, SOX2, and NESTIN, but a significantly lower expression of K3 in comparison to central corneal epithelium. Limbal epithelial cells did not express K3 after cultivation on amniotic membrane and showed a significantly lower expression of differentiation markers K12 and Cx43 in comparison to both corneal and limbal epithelium. The expression of all pluripotency markers was detectable in cultivated limbal epithelial cells, even though the expression was significantly lower than in native limbal epithelium.

Conclusions: : The human limbal epithelial cells express genes that are associated with the maintenance of pluripotency/multipotency and preserve an expression of these genes even after cultivation on amniotic membrane. Limbal epithelial stem cells may have a higher differentiation potential than previously presumed.

Keywords: cornea: epithelium • cornea: basic science • differentiation 
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