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Use of bioreactors for culturing human retinal organoids improves photoreceptor yields
BACKGROUND: The use of human pluripotent stem cell-derived retinal cells for cell therapy strategies and disease modelling relies on the ability to obtain healthy and organised retinal tissue in sufficient quantities. Generating such tissue is a lengthy process, often taking over 6 months of cell cu...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998504/ https://www.ncbi.nlm.nih.gov/pubmed/29895313 http://dx.doi.org/10.1186/s13287-018-0907-0 |
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author | Ovando-Roche, Patrick West, Emma L. Branch, Matthew J. Sampson, Robert D. Fernando, Milan Munro, Peter Georgiadis, Anastasios Rizzi, Matteo Kloc, Magdalena Naeem, Arifa Ribeiro, Joana Smith, Alexander J. Gonzalez-Cordero, Anai Ali, Robin R. |
author_facet | Ovando-Roche, Patrick West, Emma L. Branch, Matthew J. Sampson, Robert D. Fernando, Milan Munro, Peter Georgiadis, Anastasios Rizzi, Matteo Kloc, Magdalena Naeem, Arifa Ribeiro, Joana Smith, Alexander J. Gonzalez-Cordero, Anai Ali, Robin R. |
author_sort | Ovando-Roche, Patrick |
collection | PubMed |
description | BACKGROUND: The use of human pluripotent stem cell-derived retinal cells for cell therapy strategies and disease modelling relies on the ability to obtain healthy and organised retinal tissue in sufficient quantities. Generating such tissue is a lengthy process, often taking over 6 months of cell culture, and current approaches do not always generate large quantities of the major retinal cell types required. METHODS: We adapted our previously described differentiation protocol to investigate the use of stirred-tank bioreactors. We used immunohistochemistry, flow cytometry and electron microscopy to characterise retinal organoids grown in standard and bioreactor culture conditions. RESULTS: Our analysis revealed that the use of bioreactors results in improved laminar stratification as well as an increase in the yield of photoreceptor cells bearing cilia and nascent outer-segment-like structures. CONCLUSIONS: Bioreactors represent a promising platform for scaling up the manufacture of retinal cells for use in disease modelling, drug screening and cell transplantation studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0907-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5998504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59985042018-06-25 Use of bioreactors for culturing human retinal organoids improves photoreceptor yields Ovando-Roche, Patrick West, Emma L. Branch, Matthew J. Sampson, Robert D. Fernando, Milan Munro, Peter Georgiadis, Anastasios Rizzi, Matteo Kloc, Magdalena Naeem, Arifa Ribeiro, Joana Smith, Alexander J. Gonzalez-Cordero, Anai Ali, Robin R. Stem Cell Res Ther Research BACKGROUND: The use of human pluripotent stem cell-derived retinal cells for cell therapy strategies and disease modelling relies on the ability to obtain healthy and organised retinal tissue in sufficient quantities. Generating such tissue is a lengthy process, often taking over 6 months of cell culture, and current approaches do not always generate large quantities of the major retinal cell types required. METHODS: We adapted our previously described differentiation protocol to investigate the use of stirred-tank bioreactors. We used immunohistochemistry, flow cytometry and electron microscopy to characterise retinal organoids grown in standard and bioreactor culture conditions. RESULTS: Our analysis revealed that the use of bioreactors results in improved laminar stratification as well as an increase in the yield of photoreceptor cells bearing cilia and nascent outer-segment-like structures. CONCLUSIONS: Bioreactors represent a promising platform for scaling up the manufacture of retinal cells for use in disease modelling, drug screening and cell transplantation studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0907-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-13 /pmc/articles/PMC5998504/ /pubmed/29895313 http://dx.doi.org/10.1186/s13287-018-0907-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ovando-Roche, Patrick West, Emma L. Branch, Matthew J. Sampson, Robert D. Fernando, Milan Munro, Peter Georgiadis, Anastasios Rizzi, Matteo Kloc, Magdalena Naeem, Arifa Ribeiro, Joana Smith, Alexander J. Gonzalez-Cordero, Anai Ali, Robin R. Use of bioreactors for culturing human retinal organoids improves photoreceptor yields |
title | Use of bioreactors for culturing human retinal organoids improves photoreceptor yields |
title_full | Use of bioreactors for culturing human retinal organoids improves photoreceptor yields |
title_fullStr | Use of bioreactors for culturing human retinal organoids improves photoreceptor yields |
title_full_unstemmed | Use of bioreactors for culturing human retinal organoids improves photoreceptor yields |
title_short | Use of bioreactors for culturing human retinal organoids improves photoreceptor yields |
title_sort | use of bioreactors for culturing human retinal organoids improves photoreceptor yields |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998504/ https://www.ncbi.nlm.nih.gov/pubmed/29895313 http://dx.doi.org/10.1186/s13287-018-0907-0 |
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