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Efficient generation of hPSC-derived midbrain dopaminergic neurons in a fully defined, scalable, 3D biomaterial platform

Pluripotent stem cells (PSCs) have major potential as an unlimited source of functional cells for many biomedical applications; however, the development of cell manufacturing systems to enable this promise faces many challenges. For example, there have been major recent advances in the generation of...

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Autores principales: Adil, Maroof M., Rodrigues, Gonçalo M. C., Kulkarni, Rishikesh U., Rao, Antara T., Chernavsky, Nicole E., Miller, Evan W., Schaffer, David V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238378/
https://www.ncbi.nlm.nih.gov/pubmed/28091566
http://dx.doi.org/10.1038/srep40573
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author Adil, Maroof M.
Rodrigues, Gonçalo M. C.
Kulkarni, Rishikesh U.
Rao, Antara T.
Chernavsky, Nicole E.
Miller, Evan W.
Schaffer, David V.
author_facet Adil, Maroof M.
Rodrigues, Gonçalo M. C.
Kulkarni, Rishikesh U.
Rao, Antara T.
Chernavsky, Nicole E.
Miller, Evan W.
Schaffer, David V.
author_sort Adil, Maroof M.
collection PubMed
description Pluripotent stem cells (PSCs) have major potential as an unlimited source of functional cells for many biomedical applications; however, the development of cell manufacturing systems to enable this promise faces many challenges. For example, there have been major recent advances in the generation of midbrain dopaminergic (mDA) neurons from stem cells for Parkinson’s Disease (PD) therapy; however, production of these cells typically involves undefined components and difficult to scale 2D culture formats. Here, we used a fully defined, 3D, thermoresponsive biomaterial platform to rapidly generate large numbers of action-potential firing mDA neurons after 25 days of differentiation (~40% tyrosine hydroxylase (TH) positive, maturing into 25% cells exhibiting mDA neuron-like spiking behavior). Importantly, mDA neurons generated in 3D exhibited a 30-fold increase in viability upon implantation into rat striatum compared to neurons generated on 2D, consistent with the elevated expression of survival markers FOXA2 and EN1 in 3D. A defined, scalable, and resource-efficient cell culture platform can thus rapidly generate high quality differentiated cells, both neurons and potentially other cell types, with strong potential to accelerate both basic and translational research.
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spelling pubmed-52383782017-01-19 Efficient generation of hPSC-derived midbrain dopaminergic neurons in a fully defined, scalable, 3D biomaterial platform Adil, Maroof M. Rodrigues, Gonçalo M. C. Kulkarni, Rishikesh U. Rao, Antara T. Chernavsky, Nicole E. Miller, Evan W. Schaffer, David V. Sci Rep Article Pluripotent stem cells (PSCs) have major potential as an unlimited source of functional cells for many biomedical applications; however, the development of cell manufacturing systems to enable this promise faces many challenges. For example, there have been major recent advances in the generation of midbrain dopaminergic (mDA) neurons from stem cells for Parkinson’s Disease (PD) therapy; however, production of these cells typically involves undefined components and difficult to scale 2D culture formats. Here, we used a fully defined, 3D, thermoresponsive biomaterial platform to rapidly generate large numbers of action-potential firing mDA neurons after 25 days of differentiation (~40% tyrosine hydroxylase (TH) positive, maturing into 25% cells exhibiting mDA neuron-like spiking behavior). Importantly, mDA neurons generated in 3D exhibited a 30-fold increase in viability upon implantation into rat striatum compared to neurons generated on 2D, consistent with the elevated expression of survival markers FOXA2 and EN1 in 3D. A defined, scalable, and resource-efficient cell culture platform can thus rapidly generate high quality differentiated cells, both neurons and potentially other cell types, with strong potential to accelerate both basic and translational research. Nature Publishing Group 2017-01-16 /pmc/articles/PMC5238378/ /pubmed/28091566 http://dx.doi.org/10.1038/srep40573 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Adil, Maroof M.
Rodrigues, Gonçalo M. C.
Kulkarni, Rishikesh U.
Rao, Antara T.
Chernavsky, Nicole E.
Miller, Evan W.
Schaffer, David V.
Efficient generation of hPSC-derived midbrain dopaminergic neurons in a fully defined, scalable, 3D biomaterial platform
title Efficient generation of hPSC-derived midbrain dopaminergic neurons in a fully defined, scalable, 3D biomaterial platform
title_full Efficient generation of hPSC-derived midbrain dopaminergic neurons in a fully defined, scalable, 3D biomaterial platform
title_fullStr Efficient generation of hPSC-derived midbrain dopaminergic neurons in a fully defined, scalable, 3D biomaterial platform
title_full_unstemmed Efficient generation of hPSC-derived midbrain dopaminergic neurons in a fully defined, scalable, 3D biomaterial platform
title_short Efficient generation of hPSC-derived midbrain dopaminergic neurons in a fully defined, scalable, 3D biomaterial platform
title_sort efficient generation of hpsc-derived midbrain dopaminergic neurons in a fully defined, scalable, 3d biomaterial platform
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238378/
https://www.ncbi.nlm.nih.gov/pubmed/28091566
http://dx.doi.org/10.1038/srep40573
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