Completed Cells, Biochemistry & Physiology Genetics & Molecular Biology

In vivo mechanisms of epithelial tissue morphogenesis

In plain English

AI plain-English summary

A fruit fly embryo builds its own body by tightening belts of protein along cell boundaries, and researchers want to know exactly how those belts form and pull tissues into shape. This matters because biologists understand many of the genes that instruct cells what to become, but they have much less grasp of the physical forces that actually sculpt a flat sheet of cells into a three-dimensional organ or body segment. The gap is fundamental: knowing the genetic blueprint is not the same as knowing how the building gets built. The team will watch actomyosin-rich boundaries in living *Drosophila* embryos as they drive two key processes—axis extension and compartment boundary formation—and test how those boundaries repair genetic errors, orient cell division, and trigger tissue folding. This is fundamental science with no immediate practical application. But similar work on how cells generate and sense mechanical forces has already informed tissue engineering, organoid culture, and understanding of birth defects. A universal set of morphogenetic rules—combining genetics with physics—could eventually help researchers predict how human tissues form, fail, or might be repaired.

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Understanding how a tri-dimensional tissue is built from the genetic blueprint is a key frontier in biology. In addition to genes known to be important in specific aspects of morphogenesis, physical constraints and properties play a major role in building tissues. In this proposal, I aim to understand how the genetic inputs integrate with the mechanical properties of the cells and tissues to produce form. To investigate this, we study the early development of the Drosophila embryo. We have found previously that actomyosin-rich boundaries play an important role in two fundamental and conserved morphogenetic phenomena, axis extension and compartmental boundary formation. We have also found that an extrinsic force contributes to axis extension. We will build on these findings by first investigating how the actomyosin-rich boundaries form and how they might repair genetic patterns during axis extension. Second, we will ask how, during compartmentalisation, they control the planar orientation of cell division and also epithelial folding. Finally, we will examine the impact of actomyosin-rich boundaries and extrinsic forces on epithelial tissue mechanics. Our approaches will be interdisciplinary, combining genetic, quantitative and in silico analyses to find novel and universal morphogenetic rules.

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Researchers

Bénédicte Sanson (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Epithelial morphogenesis: coordinating planar polarity and tissue mechanics
Elucidating the interplay between cellular behaviour and tissue mechanics during morphogenesis
In vivo mechanisms of collective cell movement and cell sorting.
Drosophila germ-band extension as a model for understanding the integration of cell intrinsic and extrinsic forces during animal morphogenesis
3D Multiscale Mechanical Modelling of Tissue Growth.

Original classification

Investigator Award in Science

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