Regulation of epithelial tissue homeostasis by active transepithelial transport

Epithelia are intricate tissues whose function is intimately linked to mechanics. While mechanobiology has primarily focused on factors such as cell-generated contractility and mechanical properties of extracellular matrix, a interesting mechanobiological paradigm highlights the role of osmotic and mechanical pressures in shaping epithelial tissues. In our study, we developed an in vitro model of cell-coated microsized hydrogel spheres (MHSs) which allows to decipher the interplay between cellular activities and tissue mechanics. Drastic, isotropic MHS compressions were observed once the epithelia reached confluence. Further studies revealed that the compression was a process independent of cell contractility but rather regulated by active transepithelial fluid flow. Compressive stresses of about 7 kPa are generated by such an active hydraulic mechanism. Tissue homeostasis is then maintained by a fine balance between cell proliferation and extrusion. Our findings demonstrate the critical role of fluid transport in generating mechanical forces within epithelial tissues. Supported by a theoretical mechanohydraulic model, a mechanistic framework for understanding the intricate interplay between cellular processes and tissue mechanics was established. These results challenge traditional views of epithelial tissue mechanics, emphasizing the pivotal influence of osmotic and mechanical pressures in shaping tissues. We anticipate that this study will advance the understanding of epithelial tissue development, the maintenance of homeostasis, and the mechanisms underlying pathological conditions.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-11-11
DOI
https://doi.org/10.1073/pnas.2503156122
Primary Topic
Cellular Mechanics and Interactions
Type
article
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article

Regulation of epithelial tissue homeostasis by active transepithelial transport

Benoît Ladoux, Jacques Prost, Charlie Duclut, Huiqiong Wu et al.
Proceedings of the National Academy of Sciences
Cellular Mechanics and Interactions
article

Regulation of epithelial tissue homeostasis by active transepithelial transport

Benoît Ladoux, Jacques Prost, Charlie Duclut, Huiqiong Wu, René‐Marc Mège, Tien Dang, Ranjith Chilupuri, Gregory Arkowitz
article en

Abstract

Epithelia are intricate tissues whose function is intimately linked to mechanics. While mechanobiology has primarily focused on factors such as cell-generated contractility and mechanical properties of extracellular matrix, a interesting mechanobiological paradigm highlights the role of osmotic and mechanical pressures in shaping epithelial tissues. In our study, we developed an in vitro model of cell-coated microsized hydrogel spheres (MHSs) which allows to decipher the interplay between cellular activities and tissue mechanics. Drastic, isotropic MHS compressions were observed once the epithelia reached confluence. Further studies revealed that the compression was a process independent of cell contractility but rather regulated by active transepithelial fluid flow. Compressive stresses of about 7 kPa are generated by such an active hydraulic mechanism. Tissue homeostasis is then maintained by a fine balance between cell proliferation and extrusion. Our findings demonstrate the critical role of fluid transport in generating mechanical forces within epithelial tissues. Supported by a theoretical mechanohydraulic model, a mechanistic framework for understanding the intricate interplay between cellular processes and tissue mechanics was established. These results challenge traditional views of epithelial tissue mechanics, emphasizing the pivotal influence of osmotic and mechanical pressures in shaping tissues. We anticipate that this study will advance the understanding of epithelial tissue development, the maintenance of homeostasis, and the mechanisms underlying pathological conditions.

Proceedings of the National Academy of SciencesVol. 122(46)
Centre National de la Recherche Scientifique (FR), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), Université Paris Cité (FR), Sorbonne Université (FR), Max Planck Institute for the Science of Light (DE), Institut Jacques Monod (FR), Laboratoire des Biomolécules (FR)
Openalex Percentile: Top 65%
Cellular Mechanics and Interactions
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