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Professor Otger Campàs together with his colleagues from the Physics of Life (PoL) Cluster of Excellence at Technische Universität Dresden and from the University of California Santa Barbara (UCSB) have now been able to unravel another mystery surrounding the question of how cells use their sense of touch to make vital decisions during embryogenesis. Their paper has now been published in the journal Nature Materials.
A research team at the Cluster of Excellence Physics of Life of TU Dresden and the University of California, Santa Barbara, reveals how cells sense their mechanical environment as they build tissues during embryogenesis
Building tissues and organs is one of the most complex and essential tasks that cells must accomplish during embryogenesis. In this collective task, cells communicate through a variety of communication methods, including biochemical signals - similar to a cell's sense of smell - and mechanical cues - the cell's sense of touch. Researchers in a variety of disciplines have been fascinated by cell communication for decades. Professor Otger Campàs together with his colleagues from the Physics of Life (PoL) Cluster of Excellence at Technische Universität Dresden and from the University of California Santa Barbara (UCSB) have now been able to unravel another mystery surrounding the question of how cells use their sense of touch to make vital decisions during embryogenesis. Their paper has now been published in the journal Nature Materials.
Testing the surroundings
In their paper, the researchers report how cells within a living embryo mechanically test their environment and what mechanical parameters and structures they perceive. “We know a lot about how cells sense and respond to mechanical cues in a dish. However, their microenvironment is quite different within an embryo and we did not know what mechanical cues they perceive in a living tissue,” said Campàs, Chair of Tissue Dynamics and PoL Managing Director.
The mechanical cures helps cells make important decisions, such as whether or not to divide, move or even differentiate, the differentiation process by which stem cells turn into more specialized cells able to perform specific functions. Previous works revealed that stem cells placed on a synthetic substrate rely heavily on mechanical cues to make decisions: Cells on surfaces with a stiffness similar to bones became osteoblasts (bone cells), whereas cells on surfaces with a stiffness similar to brain tissue became neurons. The findings greatly advanced the field of tissue engineering as researchers used these mechanical cues to create synthetic scaffolds to coax stem cells to develop into desired outcomes. These scaffolds are used today in a variety of biomedical applications.
From a dish to the living embryo
However, a dish is not the cell’s natural habitat. While building an organism, cells are not in contact with synthetic scaffolds in a flat dish, but rather with complex living materials in three dimensions.
Over the last decade, Prof. Campàs’ research group uncovered the mechanical cues that guide cells in the complex tissues of an embryo. Using a unique technique developed in his lab, the researchers could probe the living tissue in a similar way as cells do and find out what mechanical structures the cells sense. “We first studied how cells mechanically test their micro-environment as they differentiate and build the body axis of a vertebrate, as they differentiate,” Campàs said. “Cells used different protrusions to push and pull on their environment. So we quantified how fast and strong they were pushing.” Using a ferromagnetic oil droplet that they inserted between developing cells and subjecting it to a controlled magnetic field, they were able to mimic these tiny forces and measure the mechanical response of the cells surroundings.
Sensing the tissue architecture and cells change fate
Critical to these embryonic cells’ actions is their collective physical state, which Campàs and his research group described in a previous paper to be that of an active foam, similar in consistency to soap suds or beer froth, with cells clumped together by cell adhesion and tugging of each other. What the cells are mechanically probing, Campàs and team found out, is the collective state of this “living foam” – how stiff it is and how confined the assemblage is. “And right at the moment that cells differentiate and decide to change their fate, there is a change in the material properties of the tissue that they perceive.” According to him, at the moment the cells within the tissue decide on their fate, the tissue falls its stiffness.
Going forward
What’s not yet proven in this study is the complex question of whether – and if so, how – the change in the stiffness in the embryonic environment drives the change in the cell state. “There is an interplay between the mechanical characteristics of the structures that cells collectively build, such as tissues or organs, and the decisions they make individually, as these depend on the mechanics cues that cells sense in the tissue. This interplay is at the core of how nature builds organisms.”
The findings from this study might also have important implications for tissue engineering. Potential materials that mimic the foam-like characteristics of the embryonic tissue, as opposed to the widely used synthetic polymer or gel scaffolds, may allow researchers to create more robust and sophisticated synthetic tissues, organs and implants in the lab, with the appropriate geometries and mechanical characteristics for the desired functions.
Prof. Otger Campàs
Sprecher und Geschäftsführer
Exzellenzcluster Physics of Life, TU Dresden
Tel.: +49 174 1839105
Mail: otger.campas@tu-dresden.de
Alessandro Mongera, Marie Pochitaloff, Hannah J. Gustafson, Georgina A. Stooke-Vaughan, Payam Rowghanian, Sangwoo Kim and Otger Campàs: Mechanics of the cellular microenvironment as probed by cells in vivo during zebrafish presomitic mesoderm differentiation. Nature Materials.
http://dx.doi.org/10.1038/s41563-022-01433-9
Confocal image of the presomitic mesoderm of a zebrafish embryo. N-cadherin adhesion molecules (blac ...
Campas Lab
Campas Lab
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