Effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells

Background: The limbal area of the corneal stroma has been identified as a source of mesenchymal-like stem cells, which have potential for exploitation as a cell therapy. However, the optimal culture conditions are disputed and few direct media comparisons have been performed. In this report, we eva...

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Main Authors: Sidney, Laura E., Branch, Matthew James, Dua, Harminder S., Hopkinson, Andrew
Format: Article
Published: Elsevier 2015
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Online Access:https://eprints.nottingham.ac.uk/31287/
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author Sidney, Laura E.
Branch, Matthew James
Dua, Harminder S.
Hopkinson, Andrew
author_facet Sidney, Laura E.
Branch, Matthew James
Dua, Harminder S.
Hopkinson, Andrew
author_sort Sidney, Laura E.
building Nottingham Research Data Repository
collection Online Access
description Background: The limbal area of the corneal stroma has been identified as a source of mesenchymal-like stem cells, which have potential for exploitation as a cell therapy. However, the optimal culture conditions are disputed and few direct media comparisons have been performed. In this report, we evaluated several media types to identify the optimal for inducing an in vitro stem cell phenotype. Methods: Primary human corneal stroma-derived stem cells (CSSC) were extracted from corneoscleral rims. Culture in seven different media types was compared: Dulbecco’s modified Eagle’s medium (DMEM) with 10% foetal bovine serum (FBS); M199 with 20% FBS; DMEM-F12 with 20% serum replacement, basic fibroblast growth factor and leukaemia inhibitory factor (SCM); endothelial growth medium (EGM); semi-solid MethoCult™; serum-free keratinocyte medium (K-SFM); and StemPro®-34. Effect on proliferation, morphology, protein and mRNA expression were evaluated. Results: All media supported proliferation of CSSC with the exception of K-SFM and StemPro-34. Morphology differed between media: DMEM produced large cells whereas EGM produced very small cells. Culture in M199 produced a typical mesenchymal stem cell phenotype with high expression of CD105, CD90 and CD73 but not CD34. Culture in SCM produced a phenotype more reminiscent of a progenitor cell type with expression of CD34, ABCG2, SSEA-4 and PAX6. Discussion: Culture medium can significantly influence CSSC phenotype. SCM produced a cell phenotype closest to that of a pluripotent stem cell, and we considerate to be the most appropriate for development as a clinical grade medium for the production of CSSC phenotypes suitable for cell therapy.
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spelling nottingham-312872020-05-04T20:06:16Z https://eprints.nottingham.ac.uk/31287/ Effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells Sidney, Laura E. Branch, Matthew James Dua, Harminder S. Hopkinson, Andrew Background: The limbal area of the corneal stroma has been identified as a source of mesenchymal-like stem cells, which have potential for exploitation as a cell therapy. However, the optimal culture conditions are disputed and few direct media comparisons have been performed. In this report, we evaluated several media types to identify the optimal for inducing an in vitro stem cell phenotype. Methods: Primary human corneal stroma-derived stem cells (CSSC) were extracted from corneoscleral rims. Culture in seven different media types was compared: Dulbecco’s modified Eagle’s medium (DMEM) with 10% foetal bovine serum (FBS); M199 with 20% FBS; DMEM-F12 with 20% serum replacement, basic fibroblast growth factor and leukaemia inhibitory factor (SCM); endothelial growth medium (EGM); semi-solid MethoCult™; serum-free keratinocyte medium (K-SFM); and StemPro®-34. Effect on proliferation, morphology, protein and mRNA expression were evaluated. Results: All media supported proliferation of CSSC with the exception of K-SFM and StemPro-34. Morphology differed between media: DMEM produced large cells whereas EGM produced very small cells. Culture in M199 produced a typical mesenchymal stem cell phenotype with high expression of CD105, CD90 and CD73 but not CD34. Culture in SCM produced a phenotype more reminiscent of a progenitor cell type with expression of CD34, ABCG2, SSEA-4 and PAX6. Discussion: Culture medium can significantly influence CSSC phenotype. SCM produced a cell phenotype closest to that of a pluripotent stem cell, and we considerate to be the most appropriate for development as a clinical grade medium for the production of CSSC phenotypes suitable for cell therapy. Elsevier 2015-12 Article PeerReviewed Sidney, Laura E., Branch, Matthew James, Dua, Harminder S. and Hopkinson, Andrew (2015) Effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells. Cytotherapy, 17 (12). pp. 1706-1722. ISSN 1477-2566 cornea; corneal stroma; corneal stromal stem cells; culture medium; keratocytes; mesenchymal stromal cells http://www.sciencedirect.com/science/article/pii/S1465324915010245 doi:10.1016/j.jcyt.2015.08.003 doi:10.1016/j.jcyt.2015.08.003
spellingShingle cornea; corneal stroma; corneal stromal stem cells; culture medium; keratocytes; mesenchymal stromal cells
Sidney, Laura E.
Branch, Matthew James
Dua, Harminder S.
Hopkinson, Andrew
Effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells
title Effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells
title_full Effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells
title_fullStr Effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells
title_full_unstemmed Effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells
title_short Effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells
title_sort effect of culture medium on propagation and phenotype of corneal stroma-derived stem cells
topic cornea; corneal stroma; corneal stromal stem cells; culture medium; keratocytes; mesenchymal stromal cells
url https://eprints.nottingham.ac.uk/31287/
https://eprints.nottingham.ac.uk/31287/
https://eprints.nottingham.ac.uk/31287/