PUBLICATION
            Traction forces at the cytokinetic ring regulate cell division and polyploidy in the migrating zebrafish epicardium
- Authors
 - Uroz, M., Garcia-Puig, A., Tekeli, I., Elosegui-Artola, A., Abenza, J.F., Marín-Llauradó, A., Pujals, S., Conte, V., Albertazzi, L., Roca-Cusachs, P., Raya, Á., Trepat, X.
 - ID
 - ZDB-PUB-190605-9
 - Date
 - 2019
 - Source
 - Nature Materials 18(9): 1015-1023 (Journal)
 - Registered Authors
 - Raya, Angel, Tekeli, Isil
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Zebrafish*
 - Polyploidy*
 - Cytokinesis*
 - Cell Division*
 - Pericardium/cytology*
 - Animals
 - Extracellular Matrix
 
 - PubMed
 - 31160803 Full text @ Nat. Mater.
 
            Citation
        
        
            Uroz, M., Garcia-Puig, A., Tekeli, I., Elosegui-Artola, A., Abenza, J.F., Marín-Llauradó, A., Pujals, S., Conte, V., Albertazzi, L., Roca-Cusachs, P., Raya, Á., Trepat, X. (2019) Traction forces at the cytokinetic ring regulate cell division and polyploidy in the migrating zebrafish epicardium. Nature Materials. 18(9):1015-1023.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Epithelial repair and regeneration are driven by collective cell migration and division. Both cellular functions involve tightly controlled mechanical events, but how physical forces regulate cell division in migrating epithelia is largely unknown. Here we show that cells dividing in the migrating zebrafish epicardium exert large cell-extracellular matrix (ECM) forces during cytokinesis. These forces point towards the division axis and are exerted through focal adhesions that connect the cytokinetic ring to the underlying ECM. When subjected to high loading rates, these cytokinetic focal adhesions prevent closure of the contractile ring, leading to multi-nucleation through cytokinetic failure. By combining a clutch model with experiments on substrates of different rigidity, ECM composition and ligand density, we show that failed cytokinesis is triggered by adhesion reinforcement downstream of increased myosin density. The mechanical interaction between the cytokinetic ring and the ECM thus provides a mechanism for the regulation of cell division and polyploidy that may have implications in regeneration and cancer.
            
    
        
        
    
    
    
                
                    
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