Adaptation trajectories during adhesion and spreading affect future cell states

• Published in: Scientific reports Vol. 7; no. 1; pp. 12308 - 11
• Main Authors: Bruekers, Stéphanie M. C., Bao, Min, Hendriks, José M. A., Mulder, Klaas W., Huck, Wilhelm T. S.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 26-09-2017; Nature Publishing Group
• Subjects: 14/19; 38; 631/80; 639/301/54/2295; Adaptation; Adaptation, Physiological; Cell Adhesion - physiology; Cell Culture Techniques - methods; Cell Differentiation - physiology; Cell Line; Cell Movement - physiology; Cell spreading; Collagen; Collagen - chemistry; Cytoskeleton; Environmental changes; Fibrin; Fibrin - chemistry; Gels; Gene expression; Humanities and Social Sciences; Humans; Hydrogels; Hydrogels - chemistry; Mesenchymal Stem Cells; multidisciplinary; Physical properties; Ribonucleic acid; RNA; Science; Science (multidisciplinary); Yes-associated protein
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-12467-4

Cells are complex systems in which dynamic gene expression and protein-interaction networks adapt to changes in the environment. Seeding and subsequent spreading of cells on substrates represents an example of adaptation to a major perturbation. The formation of adhesive interactions and self-organisation of the cytoskeleton during initial spreading might prime future cell behaviour. To elucidate the role of these events on later cellular behaviour, we mapped the trajectories by which cells respond to seeding on substrates with different physical properties. Our experiments on cell spreading dynamics on collagen- or fibrin-coated polyacrylamide gels and collagen or fibrin hydrogels show that on each substrate, cells follow distinct trajectories of morphological changes, culminating in fundamentally different cell states as quantified by RNA-expression levels, YAP/TAZ localisation, proliferation and differentiation propensities. The continuous adaptation of the cell to environmental cues leaves traces due to differential cellular organisation and gene expression profiles, blurring correlations between a particular physical property and cellular phenotype.