Human 3D epithelioids enable continuous long-term clonal evolution studies across multiple epithelial tissues
Ferreira, I. S.; Pradilla-Dieste, A.; Valverde-Lopez, J. A.; Abascal, F.; Ishida, Y.; Baselga, M.; Przybilla, M.; Lawson, A.; Nicola, P.; Baez-Ortega, A.; Butler, R.; Soriano-Navarro, M.; Miniter, M.; Malasi, K.; Sancho-Serra, C.; Man, C.-B.; Cameron, M.; Tadross, J. A.; Bates, A.; Harden, G.; Ince, W.; Barnet, G.; Jena, R.; Vento-Tormo, R.; Martin, J.; Mahbubani, K. T.; Saeb-Parsy, K.; Schuhmacher, A. J.; Martincorena, I.; Fernandez-Antoran, D.
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Modeling human epithelia in vitro remains challenging because current systems do not fully preserve the combination of architecture, heterogeneity, clonal composition, and long-term dynamics shown in vivo. While 3D approaches such as organoids and organotypic cultures capture important aspects of lineage differentiation and niche signaling, they often lose stable organization over time, limiting studies of long-lasting processes such as clonal evolution and cell competition. Here, we present human epithelioids as continuous long-term, 3D epithelial cultures efficiently derived from eight adult human epithelia, including trachea, skin, buccal mucosa, esophagus, blader, urethra, submandibular gland and endometrium. Using immunostaining, electron microscopy, single-cell RNA sequencing, functional assays and somatic mutation analyses, we deeply characterized human epithelioids and confirmed that they recapitulate native architecture and cell diversity, sustain regenerative capacity, and preserve donor-specific mutational landscapes, establishing a robust and versatile platform for longitudinal interrogation of clonal evolution, tissue dynamics and responses to clinically relevant perturbations, including radiotherapy and chemotherapy, over extended timescales.
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