Substrate stress relaxation regulates monolayer fluidity and leader cell formation for collectively migrating epithelia.
Frank CharbonierJunqin ZhuRaleigh SlymanCole AllanOvijit ChaudhuriPublished in: bioRxiv : the preprint server for biology (2024)
Groups of cells must coordinate their movements in order to sculpt organs during development and maintain tissues. The mechanical properties of the underlying substrate on which cells reside are known to influence key aspects of single and collective cell migration. Despite being a nearly universal feature of biological tissues, the role of viscoelasticity (i.e., fluid-like and solid-like behavior) in collective cell migration is unclear. Using tunable engineered biomaterials, we demonstrate that sheets of epithelial cells display enhanced migration on slower-relaxing (more elastic) substrates relative to faster-relaxing (more viscous) substrates. Building our understanding of tissue-substrate interactions and collective cell dynamics provides insights into approaches for tissue engineering and regenerative medicine, and therapeutic interventions to promote health and treat disease.
Keyphrases
- cell migration
- tissue engineering
- induced apoptosis
- cell cycle arrest
- single cell
- gene expression
- cell therapy
- healthcare
- public health
- machine learning
- mental health
- signaling pathway
- oxidative stress
- cell death
- deep learning
- stem cells
- structural basis
- bone marrow
- climate change
- health information
- pi k akt
- energy transfer