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September 2nd, 2025
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CNRS
cell biology
bioRxiv

Scaffolded hiPSC liver organoids recapitulating bile duct tubulogenesis and periportal architecture.

Rajendiran, H.Open in Google Scholar•Luciani, F.Open in Google Scholar•Serhrouchni, S.Open in Google Scholar•Monet, A.Open in Google Scholar•Ong, H. T.Open in Google Scholar•Zhu, J.Open in Google Scholar•Mishra, P.Open in Google Scholar•Marchand, M.Open in Google Scholar•Sahni, G.Open in Google Scholar•Arora, A.Open in Google Scholaret al.

Recapitulating the liver periportal area in vitro remains a major challenge due to its complex cellular composition and the coordinated development of both ductal and endothelial networks. Most existing bile duct organoid models fail to reproduce tubular extension and multicellular organization. Here, we present an approach that leverages biofunctionalized ECM micro-rods to scaffold the coordinated development of bile ducts, parenchymal cells, and vascular structures. Our system recapitulates key developmental stages, from the formation of the ductal plate to the emergence of elongated tubular ducts. We further demonstrate that this approach is scalable and amenable to quantitative analysis through label-free Optical Coherence Tomography combined with AI-driven 3D segmentation. We show that the ECM rod alone provides the biophysical cues to initiate the elongation of the bile ducts and the spatial structuration of the cellular organization, while the biofunctionalization with attached growth factors enhance the maturation and the connectivity of the biliary system.

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