TY - JOUR
T1 - Accelerated production of human epithelial organoids in a miniaturized spinning bioreactor
AU - Ye, Shicheng
AU - Marsee, Ary
AU - van Tienderen, Gilles S
AU - Rezaeimoghaddam, Mohammad
AU - Sheikh, Hafsah
AU - Samsom, Roos-Anne
AU - de Koning, Eelco J P
AU - Fuchs, Sabine
AU - Verstegen, Monique M A
AU - van der Laan, Luc J W
AU - van de Vosse, Frans
AU - Malda, Jos
AU - Ito, Keita
AU - Spee, Bart
AU - Schneeberger, Kerstin
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/11/18
Y1 - 2024/11/18
N2 - 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.
AB - 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.
KW - Bioreactors
KW - Cell Culture Techniques/methods
KW - Cell Differentiation
KW - Cell Proliferation
KW - Cells, Cultured
KW - Epithelial Cells/cytology
KW - Hepatocytes/cytology
KW - Humans
KW - Liver/cytology
KW - Miniaturization
KW - Organoids/metabolism
KW - Pancreas/cytology
U2 - 10.1016/j.crmeth.2024.100903
DO - 10.1016/j.crmeth.2024.100903
M3 - Article
C2 - 39561715
SN - 2667-2375
VL - 4
JO - Cell reports methods
JF - Cell reports methods
IS - 11
M1 - 100903
ER -