Benchmarking porcine pancreatic ductal organoids for drug screening applications

Primary human pancreatic ductal organoids (HPDO) have emerged as a model to study pancreas biology and model disease like pancreatitis and pancreatic cancer. Yet, donor material availability, genetic variability and a lack of extensive benchmarking to healthy and disease pancreas limits the range of applications. To address this gap, we established porcine pancreatic ductal organoids (PPDO) as a system from a reliable, genetically defined and easily obtainable source to model pancreatic ductal/progenitor biology. We benchmarked PPDO to HPDO and primary porcine pancreas using single-cell RNA sequencing (scRNA-Seq). We observed no overt phenotypic differences in PPDO derived from distinct developmental stages using extensive proteomics profiling, with a WNT/basal cell signaling enriched population characterizing PPDO. PPDO exhibited differentiation potential towards mature ductal cells and limited potential towards endocrine lineages. We used PPDO as a chemical screening platform to assess the safety of FDA-approved drugs and showed conserved toxicity of statins and α-adrenergic receptor inhibitors between PPDO and HPDO cultures. Overall, our results highlight the PPDO as a model for mammalian duct/progenitor applications.

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Publication Details

Journal
EMBO Molecular Medicine
Published
2025-11-04
DOI
https://doi.org/10.1038/s44321-025-00330-3
Citations
1
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.81
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article

Benchmarking porcine pancreatic ductal organoids for drug screening applications

Michael Sterr, Kaiyuan Yang, Eckhard Wolf, Christine von Toerne et al.
1 citations
EMBO Molecular Medicine
Single-cell and spatial transcriptomics
0.81
article

Benchmarking porcine pancreatic ductal organoids for drug screening applications

Michael Sterr, Kaiyuan Yang, Eckhard Wolf, Christine von Toerne, Elisabeth Kemter, Simone Renner, Janina Fuß, Christos Karampelias, Heiko Lickert, Sören Franzenburg, Tatsuya Kin, Mireia Molina Van den Bosch, Falk J Farkas
article en
1 citations

Abstract

Primary human pancreatic ductal organoids (HPDO) have emerged as a model to study pancreas biology and model disease like pancreatitis and pancreatic cancer. Yet, donor material availability, genetic variability and a lack of extensive benchmarking to healthy and disease pancreas limits the range of applications. To address this gap, we established porcine pancreatic ductal organoids (PPDO) as a system from a reliable, genetically defined and easily obtainable source to model pancreatic ductal/progenitor biology. We benchmarked PPDO to HPDO and primary porcine pancreas using single-cell RNA sequencing (scRNA-Seq). We observed no overt phenotypic differences in PPDO derived from distinct developmental stages using extensive proteomics profiling, with a WNT/basal cell signaling enriched population characterizing PPDO. PPDO exhibited differentiation potential towards mature ductal cells and limited potential towards endocrine lineages. We used PPDO as a chemical screening platform to assess the safety of FDA-approved drugs and showed conserved toxicity of statins and α-adrenergic receptor inhibitors between PPDO and HPDO cultures. Overall, our results highlight the PPDO as a model for mammalian duct/progenitor applications.

EMBO Molecular MedicineVol. 17(12)
Alberta Hospital Edmonton (CA), Center for Environmental Health (US), University of Alberta Hospital (CA), Helmholtz Zentrum München (DE), LMU Klinikum (DE), Christian-Albrechts-Universität zu Kiel (DE), Deutsches Diabetes-Zentrum e.V. (DE), German Center for Diabetes Research (DE), Heinrich Heine University Düsseldorf (DE), Technical University of Munich (DE), Ludwig-Maximilians-Universität München (DE)
Openalex Percentile: Top 22%
Single-cell and spatial transcriptomics
0.81
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