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Tension directs cancer cell migration over fiber alignment through energy minimization
Matthew R Zanotelli1, Joseph P Miller2, Wenjun Wang3
1Nancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, 14853, USA; Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, USA.
Cells migrate against collagen fiber alignment when tension is applied perpendicular to it. This reduces the energy needed for migration by altering matrix mechanics, guiding cell movement via energy minimization.
Area of Science:
- Cell Biology
- Biophysics
- Mechanobiology
Background:
- Cell migration is crucial for biological processes like metastasis.
- Tissue mechanics, including collagen fiber alignment and tension, influence cell migration.
- Decoupling these mechanical cues is essential for understanding their individual impacts.
Purpose of the Study:
- To investigate the individual effects of collagen fiber alignment and tension on cell migration.
- To determine how these cues influence the force and energy requirements for cell motility.
- To understand the role of energy minimization in directing cell migration through fibrous matrices.
Main Methods:
- Decoupling of collagen fiber alignment and tension in experimental models.
- Computational modeling to analyze mechanical cues and energy requirements.
- Experimental validation of computational predictions regarding cell migration pathways.
Main Results:
- Cells preferentially migrate along the axis of tension, even against collagen fiber alignment.
- Applying tension perpendicular to fiber alignment increases stored potential energy in the matrix.
- This increased potential energy reduces the cell's energy expenditure for matrix deformation during migration.
Conclusions:
- Cell migration trajectory is directed by energy minimization principles.
- Applied tension can facilitate cell migration against the direction of collagen fiber alignment.
- Findings offer insights into the bioenergetics of cell migration within fibrous extracellular matrices.
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