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Adipose-derived stem cells differentiate to keratocytes in vitro
PURPOSE: Adipose-derived stem cells (ADSC) are an abundant population of adult stem cells with the potential to differentiate into several specialized tissue types, including neural and neural crest-derived cells. This study sought to determine if ADSC express keratocyte-specific phenotypic markers...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Molecular Vision
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002955/ https://www.ncbi.nlm.nih.gov/pubmed/21179234 |
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author | Du, Yiqin Roh, Danny S. Funderburgh, Martha L. Mann, Mary M. Marra, Kacey G. Rubin, J. Peter Li, Xuan Funderburgh, James L. |
author_facet | Du, Yiqin Roh, Danny S. Funderburgh, Martha L. Mann, Mary M. Marra, Kacey G. Rubin, J. Peter Li, Xuan Funderburgh, James L. |
author_sort | Du, Yiqin |
collection | PubMed |
description | PURPOSE: Adipose-derived stem cells (ADSC) are an abundant population of adult stem cells with the potential to differentiate into several specialized tissue types, including neural and neural crest-derived cells. This study sought to determine if ADSC express keratocyte-specific phenotypic markers when cultured under conditions inducing differentiation of corneal stromal stem cells to keratocytes. METHODS: Human subcutaneous adipose tissue was obtained by lipoaspiration. ADSC were isolated by collagenase digestion and differential centrifugation. Side population cells in ADSC were demonstrated using fluorescence-activated cell sorting after staining with Hoechst 33342. Differentiation to keratocyte phenotype was induced in fibrin gels or as pellet cultures with serum-free or reduced-serum media containing ascorbate. Keratocyte-specific gene expression was characterized using western blotting, quantitative RT–PCR, and immunostaining. RESULTS: ADSC contained a side population and exhibited differentiation to adipocytes and chondrocytes indicating adult stem-cell potential. Culture of ADSC in fibrin gels or as pellets in reduced-serum medium with ascorbate and insulin induced expression of keratocan, keratan sulfate, and aldehyde dehydrogenase 3 family, member A1 (ALDH3A1), products highly expressed by differentiated keratocytes. Expression of differentiation markers was quantitatively similar to corneal stromal stem cells and occurred in both serum-free and serum containing media. CONCLUSIONS: ADSC cultured under keratocyte-differentiation conditions express corneal-specific matrix components. Expression of these unique keratocyte products suggests that ADSC can adopt a keratocyte phenotype and therefore have potential for use in corneal cell therapy and tissue engineering. |
format | Text |
id | pubmed-3002955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Vision |
record_format | MEDLINE/PubMed |
spelling | pubmed-30029552010-12-22 Adipose-derived stem cells differentiate to keratocytes in vitro Du, Yiqin Roh, Danny S. Funderburgh, Martha L. Mann, Mary M. Marra, Kacey G. Rubin, J. Peter Li, Xuan Funderburgh, James L. Mol Vis Research Article PURPOSE: Adipose-derived stem cells (ADSC) are an abundant population of adult stem cells with the potential to differentiate into several specialized tissue types, including neural and neural crest-derived cells. This study sought to determine if ADSC express keratocyte-specific phenotypic markers when cultured under conditions inducing differentiation of corneal stromal stem cells to keratocytes. METHODS: Human subcutaneous adipose tissue was obtained by lipoaspiration. ADSC were isolated by collagenase digestion and differential centrifugation. Side population cells in ADSC were demonstrated using fluorescence-activated cell sorting after staining with Hoechst 33342. Differentiation to keratocyte phenotype was induced in fibrin gels or as pellet cultures with serum-free or reduced-serum media containing ascorbate. Keratocyte-specific gene expression was characterized using western blotting, quantitative RT–PCR, and immunostaining. RESULTS: ADSC contained a side population and exhibited differentiation to adipocytes and chondrocytes indicating adult stem-cell potential. Culture of ADSC in fibrin gels or as pellets in reduced-serum medium with ascorbate and insulin induced expression of keratocan, keratan sulfate, and aldehyde dehydrogenase 3 family, member A1 (ALDH3A1), products highly expressed by differentiated keratocytes. Expression of differentiation markers was quantitatively similar to corneal stromal stem cells and occurred in both serum-free and serum containing media. CONCLUSIONS: ADSC cultured under keratocyte-differentiation conditions express corneal-specific matrix components. Expression of these unique keratocyte products suggests that ADSC can adopt a keratocyte phenotype and therefore have potential for use in corneal cell therapy and tissue engineering. Molecular Vision 2010-12-10 /pmc/articles/PMC3002955/ /pubmed/21179234 Text en Copyright © 2010 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Du, Yiqin Roh, Danny S. Funderburgh, Martha L. Mann, Mary M. Marra, Kacey G. Rubin, J. Peter Li, Xuan Funderburgh, James L. Adipose-derived stem cells differentiate to keratocytes in vitro |
title | Adipose-derived stem cells differentiate to keratocytes in vitro |
title_full | Adipose-derived stem cells differentiate to keratocytes in vitro |
title_fullStr | Adipose-derived stem cells differentiate to keratocytes in vitro |
title_full_unstemmed | Adipose-derived stem cells differentiate to keratocytes in vitro |
title_short | Adipose-derived stem cells differentiate to keratocytes in vitro |
title_sort | adipose-derived stem cells differentiate to keratocytes in vitro |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002955/ https://www.ncbi.nlm.nih.gov/pubmed/21179234 |
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