Gap junction protein connexin 43 serves as a negative marker for a stem cell-containing population of human limbal epithelial cells

¹ Ocular Surface Center, Cullen Eye Institute, Department of Ophthalmology, Baylor College of Medicine, Houston, Texas
² Department of Medical Biochemistry and Immunology, Cardiff University Medical School and The Wales Heart Research Institute, Cardiff CF41 4XN, Wales, United Kingdom

^* To whom correspondence should be addressed. E-mail: dequanl{at}bcm.edu.

	Abstract

This study evaluated whether the gap junction protein connexin (Cx) 43 could serve as a negative cell surface marker for human corneal epithelial stem cells. Cx43 expression was evaluated in corneo-limbal tissue and primary limbal epithelial cultures. Immunofluorescent staining and laser scanning confocal microscopy showed that Cx43 was strongly expressed in the corneal and limbal suprabasal epithelial cells but the basal cells of the limbal epithelium were negative. Cx43 antibody stained mainly large cells but not small cells in primary limbal epithelial cultures. As determined by semi-quantitative RT-PCR and real-time PCR, Cx43 mRNA was more abundant in the corneal than limbal epithelia, and it was expressed in higher levels in mature limbal epithelial cultures. Using GAP11, a rabbit polyclonal antibody against the Cx32 extracellular loop 2 (151-187), a sequence that is highly homologous in Cx43, the Cx43^dim and Cx43^bright cells were selected from primary limbal epithelial cultures by fluorescence-activated cell sorting and were valuated for stem cell properties. These Cx43^dim and Cx43^bright cells were confirmed by their expression levels of Cx43 protein and mRNA. The Cx43^dim cells were found to contain higher percentages of slow-cycling BrdU-label retaining cells and the cells that were positive for stem cell associated markers, p63, ABCG2 and integrin 1, and negative for differentiation markers, K3 and involucrin. The Cx43^dim cells possessed a greater proliferative potential than Cx43^bright cells and non-fractionated cells as evaluated by BrdU ncorporation, colony forming efficiency and growth capacity. Our findings suggest that human limbal basal cells do not express connexin 43, which could serve as a negative cell surface marker for the stem cell-containing population of human limbal epithelial cells.

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