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Analysis of Cell Migration within a Three-dimensional Collagen Matrix
Published on: October 5, 2014
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Highly motile cells are metabolically responsive to collagen density
Matthew R Zanotelli1,2, Jian Zhang2, Ismael Ortiz2
1Nancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853.
Summary
Tumor cell migration is linked to energy use, but only highly motile cells show this connection. Extracellular matrix mechanics dictate cell energetics and influence motility.
Area of Science:
- Cell Biology
- Biophysics
- Cancer Research
Background:
- Altered tissue mechanics and metabolism drive tumorigenesis.
- Mechanoresponsive metabolism influences cancer cell migration and metastasis.
- Tumor-associated collagen signature (increased collagen deposition) impacts cell behavior, but its effect on metabolism is unclear.
Purpose of the Study:
- To investigate the relationship between extracellular matrix mechanics, individual cell bioenergetics, and migratory phenotype.
- To clarify the impact of varying collagen densities on cell metabolism and migration.
- To determine if cell population-based measurements obscure individual cell metabolic responses.
Main Methods:
- Utilized a range of collagen densities to modulate cell migration.
- Studied individual cell bioenergetics over time using live-cell imaging.
- Sorted cells based on motility levels to analyze distinct cellular behaviors.
Main Results:
- Cellular energetics were dependent on collagen density exclusively in highly motile cells.
- Low-motility cells and the overall population did not show this direct correlation.
- Increased migration ability with higher collagen density correlated with reduced energy expenditure during movement.
Conclusions:
- A direct link exists between extracellular matrix mechanics, migratory phenotype, and cell bioenergetics.
- Energetic costs of cell movement are influenced by the extracellular matrix.
- Matrix properties significantly impact cell motility by modulating energy usage.
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