Active Cells, Biochemistry & Physiology Genetics & Molecular Biology

Mechanical regulation of cell division: Speed versus Strength

In plain English

AI plain-English summary

A living tissue’s response to being stretched depends critically on *how fast* the stretch happens, not just how far it goes. Most lab experiments yank tissues instantly, but inside the body—during embryo growth, wound healing, or the stiffening of fibrotic tissue—strain builds up slowly, over hours or days. This gap matters because the speed of mechanical change may fundamentally alter how cells decide to divide. In preliminary work, the researchers found that stretching tissue at different speeds produces markedly different division responses. They will combine custom tissue-stretching devices with mathematical models to map how strain rate, not just strain magnitude, governs cell division. This is fundamental science. There is no immediate clinical application. But the mechanisms that tune proliferation to mechanical timing are likely to be hijacked in cancer, where crowded, stiff tumour microenvironments create unusual strain patterns. Understanding how cells sense the *pace* of force could eventually reveal new targets for therapies that normalise division in diseased tissues, or improve lab-grown tissues for regenerative medicine. For now, the work opens a previously unexplored dimension of mechano-regulation.

View original technical description
Cells within biological tissues must respond to internal and external mechanical forces to maintain tissue structure, ensure tissue homeostasis and coordinate embryonic development. Mechanical regulation of cell division is emerging as a key route to control proliferation in tissues, but our knowledge of the mechanisms involved is still in its infancy. This is important considering the mechanical strains experienced in proliferating tissues during embryonic development and in common diseases, such as cancer. A major gap in our understanding is how the speed of mechanical change impacts mechano- regulation. Most studies expose cells to fast, instantaneous, changes in mechanical strain but in vivo tissues frequently experience a much slower build-up of strain, such as during morphogenesis or fibrosis. Crucially, in preliminary work, we find a marked difference in division response when tissue is stretched at different speeds. We will use a combination of tissue-stretch and tailored mathematical and computational modelling to determine how the speed versus strength of strain regulates cell division in complex tissue environments. Unravelling how tissues respond to strain rate provides a new window into the fundamentals of mechano-regulation not previously explored and will reveal mechanisms vital to tissue function that can be exploited in regenerative medicine.

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Researchers

Sarah Woolner (EPMC Awardee)

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Original classification

Career Development Award

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