Finer touch for tuning stem cell 'fate' with substrates of varying stiffness

Finer touch for tuning stem cell "fate" with substrates of varying stiffness
(top) Intracellular localization of RUNX2 and YAP in MSCs on gelatin gels with different elastic moduli. Notice how more signal is seen in a single location (the nucleus) for stiffer substrates. (bottom) Illustration of how localization of YAP and RUNX2 changes with substrate stiffness for different batches. Note the consistency between batches in how YAP localization changes with stiffness, and the lack thereof for RUNX2 before they converge. Credit: Tokyo Metropolitan University

Researchers from Tokyo Metropolitan University have been quantifying how different batches of mesenchymal stem cells respond to the mechanical stiffness of their environments. They focused on how certain proteins were "localized" in cell nuclei and found key trends in how this changed with stiffness. Their findings explain inconsistencies between previous findings and may guide how scientists control the state of stem cells for research and medical treatments.

Mesenchymal stem cells (MSCs) are important "progenitor" cells that can transform into muscle, cartilage, bone or fat cells. In 2006, pioneering work by Engler and coworkers showed that they could control what cell type mesenchymal stem cells transformed (or "differentiated") into by simply placing them on surfaces with a different mechanical stiffness, or elastic modulus. Ever since, scientists have been trying to identify exactly how this occurs. The trouble is, despite the phenomenon being robust and reproducible, it turns out that they are sensitive to the exact into which they are placed, even which batch they came from. The stakes are high: reliable control over MSC states would mean more research and even potential biomedical applications.

This inspired a team led by Associate Professor Hiromi Miyoshi of Tokyo Metropolitan University to look at how different batches of MSCs respond to . They focused on two proteins present in MSCs, the YAP protein, which helps cells respond to mechanical environments, and RUNX2, a key player in helping MSCs turn into osteoblasts which eventually become bone. They looked at how different MSC batches have different distributions of YAP and RUNX2 inside their cells. For their "stiff" environments, they chose a specially designed gelatin substrate which had significantly better reproducibility than popular collagen alternatives.

From the beginning, they found that their batches were quite distinct. In basic experiments looking at how they turned into bone-making or fat-making cells, they found that the batches produced very different levels of calcium and fat deposits. But when it came to their mechanoresponsive behavior, it turned out they were not as wildly distinct as initially thought. Firstly, the team found that the proportion of YAP found in the nuclei of cells (or "localization") turns out to vary in a consistent manner between batches, plateauing at the same stiffness. For RUNX2, though the localization varied differently, they still plateaued at a specific stiffness value (a different one to YAP). Even then, the trend in RUNX2 localization was linear up to the plateau.

With this kind of information, anyone could make a gel of a specific and actively control the level of YAP/RUNX2 in the nucleus of . By doing so, they could tune when and how their differentiate. The team hope this new level of control over cell fate will help accelerate research into MSCs and potentially lead to therapeutic applications.


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More information: Masashi YAMAZAKI et al, Designing Elastic Modulus of Cell Culture Substrate to Regulate YAP and RUNX2 Localization for Controlling Differentiation of Human Mesenchymal Stem Cells, Analytical Sciences (2021). DOI: 10.2116/analsci.20SCP02
Provided by Tokyo Metropolitan University
Citation: Finer touch for tuning stem cell 'fate' with substrates of varying stiffness (2021, May 24) retrieved 4 August 2021 from https://phys.org/news/2021-05-finer-tuning-stem-cell-fate.html
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