Abstract
Conventional static culture of organoids necessitates weekly manual passaging and results in nonhomogeneous exposure of organoids to nutrients, oxygen, and toxic metabolites. Here, we developed a miniaturized spinning bioreactor, RPMotion, specifically optimized for accelerated and cost-effective culture of epithelial organoids under homogeneous conditions. We established tissue-specific RPMotion settings and standard operating protocols for the expansion of human epithelial organoids derived from the liver, intestine, and pancreas. All organoid types proliferated faster in the bioreactor (5.2-fold, 3-fold, and 4-fold, respectively) compared to static culture while keeping their organ-specific phenotypes. We confirmed that the bioreactor is suitable for organoid establishment directly from biopsies and for long-term expansion of liver organoids. Furthermore, we showed that after accelerated expansion, liver organoids can be differentiated into hepatocyte-like cells in the RPMotion bioreactor. In conclusion, this miniaturized bioreactor enables work-, time-, and cost-efficient organoid culture, holding great promise for organoid-based fundamental and translational research and development.
| Original language | English |
|---|---|
| Article number | 100903 |
| Journal | Cell Reports Methods |
| Volume | 4 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - 18 Nov 2024 |
Bibliographical note
Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.Keywords
- Bioreactors
- Cell Culture Techniques/methods
- Cell Differentiation
- Cell Proliferation
- Cells, Cultured
- Epithelial Cells/cytology
- Hepatocytes/cytology
- Humans
- Liver/cytology
- Miniaturization
- Organoids/metabolism
- Pancreas/cytology
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