Scalable expansion of iPSC and their derivatives across multiple lineages.
Bioprocessing
Cell banking
Cell processing
Differentiation
EBiSC
Induced pluripotent stem cells
Suspension-based bioreactor
Upscaling
Journal
Reproductive toxicology (Elmsford, N.Y.)
ISSN: 1873-1708
Titre abrégé: Reprod Toxicol
Pays: United States
ID NLM: 8803591
Informations de publication
Date de publication:
09 2022
09 2022
Historique:
received:
28
12
2021
revised:
10
05
2022
accepted:
13
05
2022
pubmed:
21
5
2022
medline:
24
8
2022
entrez:
20
5
2022
Statut:
ppublish
Résumé
Induced pluripotent stem cell (iPSC) technology enabled the production of pluripotent stem cell lines from somatic cells from a range of known genetic backgrounds. Their ability to differentiate and generate a wide variety of cell types has resulted in their use for various biomedical applications, including toxicity testing. Many of these iPSC lines are now registered in databases and stored in biobanks such as the European Bank for induced pluripotent Stem Cells (EBiSC), which can streamline the quality control and distribution of these individual lines. To generate the quantities of cells for banking and applications like high-throughput toxicity screening, scalable and robust methods need to be developed to enable the large-scale production of iPSCs. 3D suspension culture platforms are increasingly being used by stem cell researchers, owing to a higher cell output in a smaller footprint, as well as simpler scaling by increasing culture volume. Here we describe our strategies for successful scalable production of iPSCs using a benchtop bioreactor and incubator for 3D suspension cultures, while maintaining quality attributes expected of high-quality iPSC lines. Additionally, to meet the increasing demand for "ready-to-use" cell types, we report recent work to establish robust, scalable differentiation protocols to cardiac, neural, and hepatic fate to enable EBiSC to increase available research tools.
Identifiants
pubmed: 35595152
pii: S0890-6238(22)00068-5
doi: 10.1016/j.reprotox.2022.05.007
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
23-35Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.