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Adult Limbal Neurosphere Cells: A Potential Autologous Cell Resource for Retinal Cell Generation
The Corneal limbus is a readily accessible region at the front of the eye, separating the cornea and sclera. Neural colonies (neurospheres) can be generated from adult corneal limbus in vitro. We have previously shown that these neurospheres originate from neural crest stem/progenitor cells and that...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182722/ https://www.ncbi.nlm.nih.gov/pubmed/25271851 http://dx.doi.org/10.1371/journal.pone.0108418 |
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author | Chen, Xiaoli Thomson, Heather Cooke, Jessica Scott, Jennifer Hossain, Parwez Lotery, Andrew |
author_facet | Chen, Xiaoli Thomson, Heather Cooke, Jessica Scott, Jennifer Hossain, Parwez Lotery, Andrew |
author_sort | Chen, Xiaoli |
collection | PubMed |
description | The Corneal limbus is a readily accessible region at the front of the eye, separating the cornea and sclera. Neural colonies (neurospheres) can be generated from adult corneal limbus in vitro. We have previously shown that these neurospheres originate from neural crest stem/progenitor cells and that they can differentiate into functional neurons in vitro. The aim of this study was to investigate whether mouse and human limbal neurosphere cells (LNS) could differentiate towards a retinal lineage both in vivo and in vitro following exposure to a developing retinal microenvironment. In this article we show that LNS can be generated from adult mice and aged humans (up to 97 years) using a serum free culture assay. Following culture with developing mouse retinal cells, we detected retinal progenitor cell markers, mature retinal/neuronal markers and sensory cilia in the majority of mouse LNS experiments. After transplantation into the sub-retinal space of neonatal mice, mouse LNS cells expressed photoreceptor specific markers, but no incorporation into host retinal tissue was seen. Human LNS cells also expressed retinal progenitor markers at the transcription level but mature retinal markers were not observed in vitro or in vivo. This data highlights that mouse corneal limbal stromal progenitor cells can transdifferentiate towards a retinal lineage. Complete differentiation is likely to require more comprehensive regulation; however, the accessibility and plasticity of LNS makes them an attractive cell resource for future study and ultimately therapeutic application. |
format | Online Article Text |
id | pubmed-4182722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41827222014-10-07 Adult Limbal Neurosphere Cells: A Potential Autologous Cell Resource for Retinal Cell Generation Chen, Xiaoli Thomson, Heather Cooke, Jessica Scott, Jennifer Hossain, Parwez Lotery, Andrew PLoS One Research Article The Corneal limbus is a readily accessible region at the front of the eye, separating the cornea and sclera. Neural colonies (neurospheres) can be generated from adult corneal limbus in vitro. We have previously shown that these neurospheres originate from neural crest stem/progenitor cells and that they can differentiate into functional neurons in vitro. The aim of this study was to investigate whether mouse and human limbal neurosphere cells (LNS) could differentiate towards a retinal lineage both in vivo and in vitro following exposure to a developing retinal microenvironment. In this article we show that LNS can be generated from adult mice and aged humans (up to 97 years) using a serum free culture assay. Following culture with developing mouse retinal cells, we detected retinal progenitor cell markers, mature retinal/neuronal markers and sensory cilia in the majority of mouse LNS experiments. After transplantation into the sub-retinal space of neonatal mice, mouse LNS cells expressed photoreceptor specific markers, but no incorporation into host retinal tissue was seen. Human LNS cells also expressed retinal progenitor markers at the transcription level but mature retinal markers were not observed in vitro or in vivo. This data highlights that mouse corneal limbal stromal progenitor cells can transdifferentiate towards a retinal lineage. Complete differentiation is likely to require more comprehensive regulation; however, the accessibility and plasticity of LNS makes them an attractive cell resource for future study and ultimately therapeutic application. Public Library of Science 2014-10-01 /pmc/articles/PMC4182722/ /pubmed/25271851 http://dx.doi.org/10.1371/journal.pone.0108418 Text en © 2014 Chen et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited. |
spellingShingle | Research Article Chen, Xiaoli Thomson, Heather Cooke, Jessica Scott, Jennifer Hossain, Parwez Lotery, Andrew Adult Limbal Neurosphere Cells: A Potential Autologous Cell Resource for Retinal Cell Generation |
title | Adult Limbal Neurosphere Cells: A Potential Autologous Cell Resource for Retinal Cell Generation |
title_full | Adult Limbal Neurosphere Cells: A Potential Autologous Cell Resource for Retinal Cell Generation |
title_fullStr | Adult Limbal Neurosphere Cells: A Potential Autologous Cell Resource for Retinal Cell Generation |
title_full_unstemmed | Adult Limbal Neurosphere Cells: A Potential Autologous Cell Resource for Retinal Cell Generation |
title_short | Adult Limbal Neurosphere Cells: A Potential Autologous Cell Resource for Retinal Cell Generation |
title_sort | adult limbal neurosphere cells: a potential autologous cell resource for retinal cell generation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182722/ https://www.ncbi.nlm.nih.gov/pubmed/25271851 http://dx.doi.org/10.1371/journal.pone.0108418 |
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