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Limbal stem cells, a review of their identification and culture for clinical use

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Abstract

The surface of the eye is covered by two distinct epithelial populations, the conjunctival and corneal epithelia. The stem cell population for the corneal epithelia has been found to be located at the area known as the limbus. This is a narrow ring of tissue at the transitional zone between the cornea and conjunctiva. This stem cell population is responsible for generating transient amplifying cells which are responsible for renewing the cornea epithelia. There are currently no definitive markers for the stem cell population in the limbus. Instead using morphological features, such as small cells with a high nucleus-to-cytoplasm ratio, in conjunction with the presence of certain markers e.g. ΔNP63α and the absence of others, e.g. the cytokeratin pair 3 & 12, are taken as being indicative of the stem cell population. Damage can occur to the corneal epithelium due to a number of causes including, Steven-Johnson syndrome, and chemical or thermal burns. This results in invasion of the cornea by the conjunctival epithelium resulting in impaired vision. In 1997 Pellegrini et al. (Lancet 349, 990) successfully used cells sheets from cultured limbal cells to successfully treat patients with corneal damage. Since then several other groups, have successfully treated patients, using similar methods.

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Acknowledgements

We would like to thank Mr William Power and Dr Andra Bobart of the Royal Victoria Eye and Ear Hospital, Dublin and Dr. Sandra Shaw of the Irish Blood Transfusion Service (IBTS) for their support in conducting our research program. We would also like to thank The Research Foundation Committee at The Royal Victoria Eye and Ear Hospital, and The Higher Education Authority of Ireland, Program for Research in Third Level Institutions (PRTLI) cycle 3, for their financial support.

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Correspondence to Finbarr O’Sullivan.

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O’Sullivan, F., Clynes, M. Limbal stem cells, a review of their identification and culture for clinical use. Cytotechnology 53, 101–106 (2007). https://doi.org/10.1007/s10616-007-9063-6

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  • DOI: https://doi.org/10.1007/s10616-007-9063-6

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