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First published online November 10, 2005
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2005-0382v1
24/4/1075    most recent
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Submitted on August 9, 2005
Accepted on October 14, 2005

Original Article

Integrins in slow cycling corneal epithelial cells at the limbus in the mouse

A. Pajoohesh-Ganji 1, S. Pal-Ghosh 1, S. J. Simmens 1, M. A. Stepp 1*

1 The George Washington University Medical Center, Washington, DC

* To whom correspondence should be addressed. E-mail: mastepp{at}gwu.edu.


   Abstract

Adult corneal epithelial stem cells (CESCs) have been shown to reside at the periphery of the cornea at a site called the corneoscleral junction or limbus. While studies have shown that these cells are slow cycling, their molecular characteristics are not well understood. Using a whole mount procedure, we show that while {alpha}9 integrin is present in a subset of the basal cells at the corneal limbus and absent in the central cornea, {beta}1, {beta}4, {alpha}3, and {alpha}6 integrins are more highly expressed overall in central corneal basal cells. To characterize CESCs based on their slow-cycling nature, we simultaneously evaluated 5Bromo-2-deoxy-uridine (BrdU) label-retaining cells (LRCs) and integrin expression ({alpha}9, {beta}1 and {beta}4) in a total of 1889 cells at the limbus of adult mice that had been injected as neonates with BrdU. While the LRCs were usually observed adjacent to {alpha}9 integrin positive cells, most LRCs were {alpha}9 integrin negative and expressed high levels of {beta}1 and {beta}4 integrins. In addition, we observed more BrdU-positive LRCs at the superior and inferior quadrants of adult mouse corneas than at the nasal and temporal quadrants, and determined that 0.94 to 3.6% of the limbal basal cells were slow-cycling. We conclude from these data that the slow cycling LRCs in the adult mouse cornea are enriched in cells that express high levels of {beta}1 and {beta}4 integrins and little {alpha}9 integrin.

Key Words. adhesion receptors, integrins, mouse




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