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Title: CD200 Expression Marks a Population of Quiescent Limbal Epithelial Stem Cells with Holoclone Forming Ability
Authors: Bojic, Sanja
Hallam D.
Alcada N.
Ghareeb A.
Queen R.
Pervinder S.
Buck H.
Amitai Lange A.
Figueiredo G.
Rooney P.
Stojkovíc M.
Shortt A.
Figueiredo F.
lako, majlinda
Journal: Stem Cells
Issue Date: 1-Nov-2018
Abstract: ©2018 The Authors STEM CELLS published by Wiley Periodicals, Inc. on behalf of AlphaMed Press 2018 One of the main challenges in limbal stem cell (LSC) biology and transplantation is the lack of definitive cell surface markers which can be used to identify and enrich viable LSCs. In this study, expression of 361 cell surface proteins was assessed in ex vivo expanded limbal epithelial cells. One marker, CD200 was selected for further characterization based on expression in a small subset of limbal epithelial cells (2.25% ± 0.69%) and reduced expression through consecutive passaging and calcium induced differentiation. CD200 was localized to a small population of cells at the basal layer of the human and mouse limbal epithelium. CD200+cells were slow cycling and contained the majority of side population (SP) and all the holoclone forming progenitors. CD200+ cells displayed higher expression of LSCs markers including PAX6, WNT7A, CDH3, CK14, CK15, and ABCB5 and lower expression of Ki67 when compared to CD200−. Downregulation of CD200 abrogated the ability of limbal epithelial cells to form holoclones, suggesting an important function for CD200 in the maintenance and/or self-renewal of LSCs. A second marker, CD109, which was expressed in 56.29% ± 13.96% of limbal epithelial cells, was also found to co-localize with ΔNp63 in both human and mouse cornea, albeit more abundantly than CD200. CD109 expression decreased slowly through calcium induced cell differentiation and CD109+ cells were characterized by higher expression of Ki67, when compared to CD109− subpopulation. Together our data suggest that CD200 expression marks a quiescent population of LSCs with holoclone forming potential, while CD109 expression is associated with a proliferative progenitor phenotype. Stem Cells 2018;36:1723–1735.
Type: Article
DOI: 10.1002/stem.2903
ISSN: 10665099
SCOPUS: 85054312313
Appears in Collections:Faculty of Medical Sciences, Kragujevac
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