Osmotic pressure induces unexpected relaxation of contractile 3D microtissue

Cell contraction and proliferation, matrix secretion and external mechanical forces induce compression during embryogenesis and tumor growth, which in turn regulate cell proliferation, metabolism or differentiation. How compression affects tissue contractility, a hallmark of tissue function, is however unknown. Here we apply osmotic compression to microtissues of either mouse colon adenocarcinoma CT26 cells, mouse NIH 3T3 fibroblasts, or human primary colon cancer-associated fibroblasts. Microtissues are anchored to flexible pillars that serve as force transducers. We observe that low-amplitude osmotic compression induces a rapid relaxation of tissue contractility, primed by the deformation of the extracellular matrix. Furthermore, we show that this compression-induced relaxation is independent of the cell type, proportional to the initial tissue contractility, and depends on RhoA-mediated myosin activity. Together, our results demonstrate that compressive stress can relax active tissue force, and points to a potential role of this feedback mechanism during morphogenetic events such as onco- or embryogenesis.

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Publication Details

Journal
The European Physical Journal E
Published
2025-06-24
DOI
https://doi.org/10.1140/epje/s10189-025-00497-0
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Osmotic pressure induces unexpected relaxation of contractile 3D microtissue

Ben Fabry, Jonathan Fouchard, Simon de Beco, Martial Balland et al.
The European Physical Journal E
3D Printing in Biomedical Research
article

Osmotic pressure induces unexpected relaxation of contractile 3D microtissue

Ben Fabry, Jonathan Fouchard, Simon de Beco, Martial Balland, D. Ambrosi, Pietro Mascheroni, Giovanni Cappello, Thomas Boudou, Pierre Recho, Ayman Radwan, Fanny Wodrascka, Genesis Marquez-Vivas, Parvathy Anoop
article en

Abstract

Cell contraction and proliferation, matrix secretion and external mechanical forces induce compression during embryogenesis and tumor growth, which in turn regulate cell proliferation, metabolism or differentiation. How compression affects tissue contractility, a hallmark of tissue function, is however unknown. Here we apply osmotic compression to microtissues of either mouse colon adenocarcinoma CT26 cells, mouse NIH 3T3 fibroblasts, or human primary colon cancer-associated fibroblasts. Microtissues are anchored to flexible pillars that serve as force transducers. We observe that low-amplitude osmotic compression induces a rapid relaxation of tissue contractility, primed by the deformation of the extracellular matrix. Furthermore, we show that this compression-induced relaxation is independent of the cell type, proportional to the initial tissue contractility, and depends on RhoA-mediated myosin activity. Together, our results demonstrate that compressive stress can relax active tissue force, and points to a potential role of this feedback mechanism during morphogenetic events such as onco- or embryogenesis.

The European Physical Journal EVol. 48(6-7)
Centre National de la Recherche Scientifique (FR), Politecnico di Torino (IT), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), Université Paris Cité (FR), Sorbonne Université (FR), Institut de Biologie Paris-Seine (FR), Laboratoire Interdisciplinaire de Physique (FR), Institut Jacques Monod (FR), Université Grenoble Alpes (FR)
Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Institut des sciences de l'ingénierie et des systèmes, H2020 Marie Skłodowska-Curie Actions
Good health and well-being
Openalex Percentile: Top 86%
3D Printing in Biomedical Research
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