Accelerated maturation of branched organoids confined in collagen droplets

Droplet-based organoid culture offers several advantages over conventional bulk organoid culture, such as improved yield, reproducibility, and throughput. However, organoids grown in droplets typically display only a spherical geometry and lack the intricate structural complexity found in native tissue. By incorporating singularised pancreatic ductal adenocarcinoma cells into collagen droplets, we achieve the growth of branched structures, indicating a more complex interaction with the surrounding hydrogel. A comparison of organoid growth in droplets of different diameters showed that while geometrical confinement improves organoid homogeneity, it also impairs the formation of more complex organoid morphologies. Thus, only in 750 μm diameter collagen droplets did we achieve the consistent growth of highly branched structures with a morphology closely resembling the structural complexity achieved in traditional bulk organoid culture. Moreover, our analysis of organoid morphology and transcriptomic data suggests an accelerated maturation of organoids cultured in collagen droplets, highlighting a shift in developmental timing compared to traditional systems.

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Publication Details

Journal
Lab on a Chip
Published
2025-01-01
DOI
https://doi.org/10.1039/d5lc00287g
Primary Topic
Tissue Engineering and Regenerative Medicine
Type
article
Field-Weighted Citation Impact
0.00

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article

Accelerated maturation of branched organoids confined in collagen droplets

Anna Pastucha, Andreas R. Bausch, David A. Weitz, Iris Ruider et al.
Lab on a Chip
Tissue Engineering and Regenerative Medicine
article

Accelerated maturation of branched organoids confined in collagen droplets

Anna Pastucha, Andreas R. Bausch, David A. Weitz, Iris Ruider, Maximilian Reichert, Marion Raich, Wentao Xu, Yan Liu
article en

Abstract

Droplet-based organoid culture offers several advantages over conventional bulk organoid culture, such as improved yield, reproducibility, and throughput. However, organoids grown in droplets typically display only a spherical geometry and lack the intricate structural complexity found in native tissue. By incorporating singularised pancreatic ductal adenocarcinoma cells into collagen droplets, we achieve the growth of branched structures, indicating a more complex interaction with the surrounding hydrogel. A comparison of organoid growth in droplets of different diameters showed that while geometrical confinement improves organoid homogeneity, it also impairs the formation of more complex organoid morphologies. Thus, only in 750 μm diameter collagen droplets did we achieve the consistent growth of highly branched structures with a morphology closely resembling the structural complexity achieved in traditional bulk organoid culture. Moreover, our analysis of organoid morphology and transcriptomic data suggests an accelerated maturation of organoids cultured in collagen droplets, highlighting a shift in developmental timing compared to traditional systems.

Lab on a ChipVol. 25(19)
Harvard University (US), German Cancer Research Center (DE), Heidelberg University (DE), TUM Klinikum (DE), Max Planck Institute of Psychiatry (DE), Inspire Institute (US), Technical University of Munich (DE)
European Commission, Bundesministerium für Bildung und Forschung, Innovation and Technology Commission, Max-Planck-Gesellschaft, Westfälische Wilhelms-Universität Münster, Technische Universität München, Hansjörg Wyss Institute for Biologically Inspired Engineering, Harvard University, H2020 European Research Council
Openalex Percentile: Top 69%
Tissue Engineering and Regenerative Medicine
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