Conjunctival epithelial cells maintain stem cell properties after long-term culture and cryopreservation. (September 2009)

• Record Type: Journal Article
• Authors: Schrader, S; Notara, M; Beaconsfield, M; Tuft, S; Geerling, G; Daniels, JT
• Is Part Of: Regenerative medicine. Volume 4:Number 5(2009)
• Page Start: 677
• Page End: 687
• Publication Date: 2009-09
• Subjects: cell therapy -- conjunctiva -- in vitro culture -- stem cell -- tissue engineering; Cellular therapy -- Periodicals; Stem cells -- Transplantation -- Periodicals; Degeneration (Pathology) -- Treatment -- Periodicals; Regeneration (Biology) -- Periodicals; 611.018
• DOI: 10.2217/rme.09.39
• Languages: English
• ISSNs: 1746-0751

Abstract

Aim: Transplantation of tissue-engineered conjunctival epithelial cell sheets has proven to be a promising technique for conjunctival reconstruction. The ability to cryopreserve conjunctival epithelial cells and maintain their stem cell population would improve their availability for clinical use. The aim of this study was to evaluate whether cryopreservation and long-term in vitro culture has an effect on the proliferative capacity and the progenitor-like cell characteristics of conjunctival epithelial cells.Method: Human conjunctival cells from bulbar biopsies were isolated and expanded on a growth arrested 3T3 feeder layer. The cells were evaluated for cytokeratin (CK4/CK19) expression by immunostaining. An aliquot with half of the cells from the initial culture was frozen in liquid nitrogen and stored for 14 days and, in addition, donor cells were cryopreserved for more than 6 months (202.7 ±± 13.0 days). Both cryopreserved and noncryopreserved cells were serially cultivated over four passages. For each passage the colony-forming efficiency and the cell population doubling rates were evaluated, and expression of putative progenitor cell markers, p63αα and ABCG2, was assessed by immunostaining and reverse transcription PCR.Results: Both noncryopreserved and cryopreserved cells demonstrated a high colony-forming capacity that decreased with passage. Cells from both groups underwent approximately 20 cell population doublings before senescence. Immunoreactivity to p63αα and ABCG2 was found in both groups until passage 4 and their presence was also confirmed by reverse transcription PCR. No difference in cell viability, colony-forming efficiency and immunoreactivity to p63αα and ABCG2 was observed between cells cryopreserved for 14 days, and more than 6 months (202.7 ±± 13.0 days).Conclusion: Conjunctival epithelial cells with progenitor cell-like characteristics can be efficiently cryopreserved and can subsequently maintain their function in vitro over several culture passages. The option to cryopreserve conjunctival cells prior to in vitro expansion would be an advantage when cells have to be cultivated for clinical transplantation.