Spatiotemporal analyses of cellular tractions describe subcellular effect of substrate stiffness and coating
| Autor: | Marie-Mo Vaeyens, Alvaro Jorge-Peñas, Ramesh Subramani, Diego A. Vargas, Hans Van Oosterwyck, Alicia Izquierdo-Álvarez |
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| Rok vydání: | 2019 |
| Předmět: |
Polyacrylamide Hydrogel
Focus (geometry) genetic structures 0206 medical engineering Traction (engineering) Biomedical Engineering 02 engineering and technology engineering.material Traction force microscopy Coating Traction Human Umbilical Vein Endothelial Cells medicine Humans biology Chemistry technology industry and agriculture Stiffness Hydrogels 020601 biomedical engineering eye diseases Fibronectins Fibronectin surgical procedures operative Self-healing hydrogels biology.protein Biophysics engineering Stress Mechanical sense organs medicine.symptom |
| Popis: | Cells interplay with their environment through mechanical and chemical interactions. To characterize this interplay, endothelial cells were cultured on polyacrylamide hydrogels of varying stiffness, coated with either fibronectin or collagen. We developed a novel analysis technique, complementary to traction force microscopy, to characterize the spatiotemporal evolution of cellular tractions: We identified subpopulations of tractions, termed traction foci, and tracked their magnitude and lifetime. Each focus consists of tractions associated with a local single peak of maximal traction. Individual foci were spread over a larger area in cells cultured on collagen relative to those on fibronectin and exerted higher tractions on stiffer hydrogels. We found that the trends with which forces increased with increasing hydrogel stiffness were different for foci and whole-cell measurements. These differences were explained by the number of foci and their average strength. While on fibronectin multiple short-lived weak foci contributed up to 30% to the total traction on hydrogels with intermediate stiffness, short-lived foci in such a number were not observed on collagen despite the higher tractions. Our approach allows for the use of existing traction force microscopy data to gain insight at the subcellular scale without molecular probes or spatial constraining of cellular tractions. ispartof: Annals of Biomedical Engineering vol:47 issue:2 pages:624-637 ispartof: location:United States status: published |
| Databáze: | OpenAIRE |
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