# Molecular tension indicators reveal unexpectedly complex regulation of tension in live mouse organs

**Authors:** Keita Fujiwara, Katsunori Fujiki, Tomoya O. Akama, Katsuhiko Shirahige, Ichiro Shiojima, Tomoyuki Nakamura, Maretoshi Hirai

PMC · DOI: 10.1038/s42003-026-09746-0 · 2026-02-19

## TL;DR

New molecular tension indicators reveal that mechanical forces in mouse organs are regulated in complex and varied ways.

## Contribution

A FRET-free molecular tension sensor was developed for high-resolution in vivo visualization of mechanical forces.

## Key findings

- The new sensor allows visualization of subtle tension changes from color tone under superresolution microscopy.
- H11 knock-in mice showed molecule-specific and heterogeneous regulation of mechanical load in tissues.
- Mechanical force regulation in live mouse organs is more complex than previously understood.

## Abstract

Since the emergence of molecular tension sensors, the understanding of mechanical forces has advanced substantially. However, visualizing molecular tension in mammalian tissues has remained challenging owing to the technical constraints of the Förster resonance energy transfer (FRET)-based molecular tension sensors. Here, we develop a molecular tension sensor based on circularly permuted EGFP with an elastic linker, which is inserted into either αActinin or αCatenin and then fused with mCherry at the C-terminus to simultaneously visualize tension and the amount of sensor protein. This single-fluorophore tension indicator enables subtle tension changes to be visualized simply from color tone under superresolution microscopy. We further generate H11 knock-in mice expressing these indicators, revealing a molecular-specific regulation of mechanical load within tissues. Thus, our molecular tension indicators provide a powerful approach for probing the complex and heterogeneous regulation of mechanical forces in vivo mammalian systems.

FRET-free molecular tension indicators enable high-resolution visualization of tension in vivo, revealing that the regulation of mechanical forces is unexpectedly complex, molecule-specific and heterogeneous in live mouse organs.

## Linked entities

- **Genes:** actn1.L (actinin alpha 1 L homeolog) [NCBI Gene 399422], H1-1 (H1.1 linker histone, cluster member) [NCBI Gene 3024]
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** H1-1 (H1.1 linker histone, cluster member) [NCBI Gene 3024] {aka H1.1, H1A, H1F1, HIST1, HIST1H1A}
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13031782/full.md

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Source: https://tomesphere.com/paper/PMC13031782