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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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.
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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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