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Transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro
PURPOSE: The aim of this study was to investigate whether cells originating from human embryonic stem cells (hESCs) could be successfully transplanted onto a partially wounded human cornea. A second aim was to study the ability of the transplanted cells to differentiate into corneal epithelial-like...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660785/ https://www.ncbi.nlm.nih.gov/pubmed/22280565 http://dx.doi.org/10.1111/j.1755-3768.2011.02358.x |
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author | Hanson, Charles Hardarson, Thorir Ellerström, Catharina Nordberg, Markus Caisander, Gunilla Rao, Mahendra Hyllner, Johan Stenevi, Ulf |
author_facet | Hanson, Charles Hardarson, Thorir Ellerström, Catharina Nordberg, Markus Caisander, Gunilla Rao, Mahendra Hyllner, Johan Stenevi, Ulf |
author_sort | Hanson, Charles |
collection | PubMed |
description | PURPOSE: The aim of this study was to investigate whether cells originating from human embryonic stem cells (hESCs) could be successfully transplanted onto a partially wounded human cornea. A second aim was to study the ability of the transplanted cells to differentiate into corneal epithelial-like cells. METHODS: Spontaneously, differentiated hESCs were transplanted onto a human corneal button (without limbus) with the epithelial layer partially removed. The cells were cultured on Bowman’s membrane for up to 9 days, and the culture dynamics documented in a time-lapse system. As the transplanted cells originated from a genetically engineered hESC line, they all expressed green fluorescent protein, which facilitated their identification during the culture experiments, tissue preparation and analysis. To detect any differentiation into human corneal epithelial-like cells, we analysed the transplanted cells by immunohistochemistry using antibodies specific for CK3, CK15 and PAX6. RESULTS: The transplanted cells established and expanded on Bowman’s membrane, forming a 1–4 cell layer surrounded by host corneal epithelial cells. Expression of the corneal marker PAX6 appeared 3 days after transplantation, and after 6 days, the cells were expressing both PAX6 and CK3. CONCLUSION: This shows that it is possible to transplant cells originating from hESCs onto Bowman’s membrane with the epithelial layer partially removed and to get these cells to establish, grow and differentiate into corneal epithelial-like cells in vitro. |
format | Online Article Text |
id | pubmed-3660785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36607852013-05-22 Transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro Hanson, Charles Hardarson, Thorir Ellerström, Catharina Nordberg, Markus Caisander, Gunilla Rao, Mahendra Hyllner, Johan Stenevi, Ulf Acta Ophthalmol Original Articles PURPOSE: The aim of this study was to investigate whether cells originating from human embryonic stem cells (hESCs) could be successfully transplanted onto a partially wounded human cornea. A second aim was to study the ability of the transplanted cells to differentiate into corneal epithelial-like cells. METHODS: Spontaneously, differentiated hESCs were transplanted onto a human corneal button (without limbus) with the epithelial layer partially removed. The cells were cultured on Bowman’s membrane for up to 9 days, and the culture dynamics documented in a time-lapse system. As the transplanted cells originated from a genetically engineered hESC line, they all expressed green fluorescent protein, which facilitated their identification during the culture experiments, tissue preparation and analysis. To detect any differentiation into human corneal epithelial-like cells, we analysed the transplanted cells by immunohistochemistry using antibodies specific for CK3, CK15 and PAX6. RESULTS: The transplanted cells established and expanded on Bowman’s membrane, forming a 1–4 cell layer surrounded by host corneal epithelial cells. Expression of the corneal marker PAX6 appeared 3 days after transplantation, and after 6 days, the cells were expressing both PAX6 and CK3. CONCLUSION: This shows that it is possible to transplant cells originating from hESCs onto Bowman’s membrane with the epithelial layer partially removed and to get these cells to establish, grow and differentiate into corneal epithelial-like cells in vitro. Blackwell Publishing Ltd 2013-03 /pmc/articles/PMC3660785/ /pubmed/22280565 http://dx.doi.org/10.1111/j.1755-3768.2011.02358.x Text en © 2012 The Authors. Acta Ophthalmologica © 2012 Acta Ophthalmologica Scandinavica Foundation http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Hanson, Charles Hardarson, Thorir Ellerström, Catharina Nordberg, Markus Caisander, Gunilla Rao, Mahendra Hyllner, Johan Stenevi, Ulf Transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro |
title | Transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro |
title_full | Transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro |
title_fullStr | Transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro |
title_full_unstemmed | Transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro |
title_short | Transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro |
title_sort | transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660785/ https://www.ncbi.nlm.nih.gov/pubmed/22280565 http://dx.doi.org/10.1111/j.1755-3768.2011.02358.x |
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