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High-throughput 3D screening for differentiation of hPSC-derived cell therapy candidates
The emergence of several cell therapy candidates in the clinic is an encouraging sign for human diseases/disorders that currently have no effective treatment; however, scalable production of these cell therapies has become a bottleneck. To overcome this barrier, three-dimensional (3D) cell culture s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413735/ https://www.ncbi.nlm.nih.gov/pubmed/32821815 http://dx.doi.org/10.1126/sciadv.aaz1457 |
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author | Muckom, Riya Bao, Xiaoping Tran, Eric Chen, Evelyn Murugappan, Abirami Dordick, Jonathan S. Clark, Douglas S. Schaffer, David V. |
author_facet | Muckom, Riya Bao, Xiaoping Tran, Eric Chen, Evelyn Murugappan, Abirami Dordick, Jonathan S. Clark, Douglas S. Schaffer, David V. |
author_sort | Muckom, Riya |
collection | PubMed |
description | The emergence of several cell therapy candidates in the clinic is an encouraging sign for human diseases/disorders that currently have no effective treatment; however, scalable production of these cell therapies has become a bottleneck. To overcome this barrier, three-dimensional (3D) cell culture strategies have been considered for enhanced cell production. Here, we demonstrate a high-throughput 3D culture platform used to systematically screen 1200 culture conditions with varying doses, durations, dynamics, and combinations of signaling cues to derive oligodendrocyte progenitor cells and midbrain dopaminergic neurons from human pluripotent stem cells (hPSCs). Statistical models of the robust dataset reveal previously unidentified patterns about cell competence to Wnt, retinoic acid, and sonic hedgehog signals, and their interactions, which may offer insights into the combinatorial roles these signals play in human central nervous system development. These insights can be harnessed to optimize production of hPSC-derived cell replacement therapies for a range of neurological indications. |
format | Online Article Text |
id | pubmed-7413735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74137352020-08-19 High-throughput 3D screening for differentiation of hPSC-derived cell therapy candidates Muckom, Riya Bao, Xiaoping Tran, Eric Chen, Evelyn Murugappan, Abirami Dordick, Jonathan S. Clark, Douglas S. Schaffer, David V. Sci Adv Research Articles The emergence of several cell therapy candidates in the clinic is an encouraging sign for human diseases/disorders that currently have no effective treatment; however, scalable production of these cell therapies has become a bottleneck. To overcome this barrier, three-dimensional (3D) cell culture strategies have been considered for enhanced cell production. Here, we demonstrate a high-throughput 3D culture platform used to systematically screen 1200 culture conditions with varying doses, durations, dynamics, and combinations of signaling cues to derive oligodendrocyte progenitor cells and midbrain dopaminergic neurons from human pluripotent stem cells (hPSCs). Statistical models of the robust dataset reveal previously unidentified patterns about cell competence to Wnt, retinoic acid, and sonic hedgehog signals, and their interactions, which may offer insights into the combinatorial roles these signals play in human central nervous system development. These insights can be harnessed to optimize production of hPSC-derived cell replacement therapies for a range of neurological indications. American Association for the Advancement of Science 2020-08-07 /pmc/articles/PMC7413735/ /pubmed/32821815 http://dx.doi.org/10.1126/sciadv.aaz1457 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Muckom, Riya Bao, Xiaoping Tran, Eric Chen, Evelyn Murugappan, Abirami Dordick, Jonathan S. Clark, Douglas S. Schaffer, David V. High-throughput 3D screening for differentiation of hPSC-derived cell therapy candidates |
title | High-throughput 3D screening for differentiation of hPSC-derived cell therapy candidates |
title_full | High-throughput 3D screening for differentiation of hPSC-derived cell therapy candidates |
title_fullStr | High-throughput 3D screening for differentiation of hPSC-derived cell therapy candidates |
title_full_unstemmed | High-throughput 3D screening for differentiation of hPSC-derived cell therapy candidates |
title_short | High-throughput 3D screening for differentiation of hPSC-derived cell therapy candidates |
title_sort | high-throughput 3d screening for differentiation of hpsc-derived cell therapy candidates |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413735/ https://www.ncbi.nlm.nih.gov/pubmed/32821815 http://dx.doi.org/10.1126/sciadv.aaz1457 |
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