Mechanobiological mechanism of cyclic stretch-induced cell columnarization

In vivo, epithelial cells maintain structural integrity under dynamic mechanical perturbations. To study this, we treated various epithelial cell lines with long-term cyclic stretch (CS). Surprisingly, cells transitioned from cuboidal to columnar shape (columnarization) in MDCK cells, while others only elongated. This change correlated with actin accumulation at the top and stress fiber realignment at the bottom. Blocking mechanical stimulation via FAK inhibition or reducing vinculin partially prevented columnarization; however, disrupting tight junctions or cellular contractility substantially blocked it. The MK4 cells, derived from MDCK cells with weaker cell-cell junctions, showed less columnarization under CS, whereas overexpressing Caveolin-1 (Cav1) in MK4 cells enhanced junctions and promoted columnar formation. Atomic force microscopy studies revealed increased apical junctional stiffness in both CS-treated MDCK and Cav1-overexpressing MK4 cells. This, combined with a mathematical model, elucidated the physical characteristics and changes in cell tension post-stretch, revealing the mechanobiological foundation of epithelial cell columnarization.

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Publication Details

Journal
Cell Reports
Published
2025-05-01
DOI
https://doi.org/10.1016/j.celrep.2025.115662
Citations
4
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
4.61
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Mechanobiological mechanism of cyclic stretch-induced cell columnarization

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article

Mechanobiological mechanism of cyclic stretch-induced cell columnarization

L. James Lee, Fu-Lai Wen, Chia-hsuan Lu, Gang‐Hui Lee, Keng-hui Lin, Ming‐Jer Tang, I-Hsiu Su
article en
4 citations

Abstract

In vivo, epithelial cells maintain structural integrity under dynamic mechanical perturbations. To study this, we treated various epithelial cell lines with long-term cyclic stretch (CS). Surprisingly, cells transitioned from cuboidal to columnar shape (columnarization) in MDCK cells, while others only elongated. This change correlated with actin accumulation at the top and stress fiber realignment at the bottom. Blocking mechanical stimulation via FAK inhibition or reducing vinculin partially prevented columnarization; however, disrupting tight junctions or cellular contractility substantially blocked it. The MK4 cells, derived from MDCK cells with weaker cell-cell junctions, showed less columnarization under CS, whereas overexpressing Caveolin-1 (Cav1) in MK4 cells enhanced junctions and promoted columnar formation. Atomic force microscopy studies revealed increased apical junctional stiffness in both CS-treated MDCK and Cav1-overexpressing MK4 cells. This, combined with a mathematical model, elucidated the physical characteristics and changes in cell tension post-stretch, revealing the mechanobiological foundation of epithelial cell columnarization.

Cell ReportsVol. 44(5)
University of Oxford (GB), Institute of Physics, Academia Sinica (TW), National Center for Theoretical Sciences (TW), National Cheng Kung University (TW)
Zero hunger
Openalex Percentile: Top 6%
Cellular Mechanics and Interactions
4.61
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