The control of chromosome segregation during mitosis in epithelial cells by substrate elasticity

• Published in: Biomaterials Vol. 33; no. 3; pp. 798 - 809
• Main Authors: Kocgozlu, Leyla, Rabineau, Morgane, Koenig, Géraldine, Haikel, Youssef, Schaaf, Pierre, Freund, Jean-Noel, Voegel, Jean-Claude, Lavalle, Philippe, Vautier, Dominique
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Ltd 01.01.2012; Elsevier
• Subjects: Advanced Basic Science; Animals; Apoptosis; Biocompatible Materials - metabolism; Biomaterials; Blotting, Western; Cancer; Cell Line; Cell migration; Chromosome missegregation; Chromosome Segregation - genetics; Chromosome Segregation - physiology; Dentistry; Elastic Modulus - physiology; Epithelial Cells - cytology; Epithelial Cells - metabolism; Integrin; Life Sciences; Mitosis - genetics; Mitosis - physiology; Polyelectrolyte multilayer films; Rats; Spindle Apparatus - metabolism; Substrate elasticity; Substrate elasticity; Integrin; Chromosome missegregation; Polyelectrolyte multilayer films; Biomaterials; Apoptosis
• ISSN: 0142-9612; 1878-5905
• DOI: 10.1016/j.biomaterials.2011.10.024

Abstract Materials of defined elasticity, including synthetic material scaffolds and tissue-derived matrices, can regulate biological responses of cells and in particular adhesion, migration, growth and differentiation which are essential parameters for tissue integration. These responses have been extensively investigated in interphase cells, but little is known whether and how material elasticity affects mitotic cells. We used polyelectrolyte multilayer films as model substrates with elastic modulus ranging from Eap = 0 up to Eap = 500 kPa and mitotic PtK2 epithelial cells to address these important questions. Soft substrates (Eap < 50 kPa) led to abnormal morphology in chromosome segregation, materialized by chromatin bridges and chromosome lagging. Frequency of these damages increased with decreasing substrate stiffness and was correlated with a pro-apoptotic phenotype. Mitotic spindle was not observed on soft substrates where formation of chromatin damages is due to low β1-integrin engagement and decrease of Rac1 activities. This work constitutes the first evidence that soft substrates hinder epithelial cell division. In perspective, our findings emphasize the prime incidence of the material elasticity on the fate of the phenotype, especially of stem cells in the mitotic phase.