PUBLICATION
            Vinculin controls endothelial cell junction dynamics during vascular lumen formation
- Authors
- Kotini, M.P., van der Stoel, M.M., Yin, J., Han, M.K., Kirchmaier, B., de Rooij, J., Affolter, M., Huveneers, S., Belting, H.G.
- ID
- ZDB-PUB-220414-8
- Date
- 2022
- Source
- Cell Reports 39: 110658 (Journal)
- Registered Authors
- Affolter, Markus, Belting, Heinz-Georg Paul (Henry), Huveneers, Stephan, Kirchmaier, Bettina, van der Stoel, Miesje
- Keywords
- CP: Cell biology, VE-cadherin, angiogenesis, cell-cell adhesion, junctional dynamics, lumenization, vinculin, zebrafish
- MeSH Terms
- 
    
        
        
            
                - Adherens Junctions/metabolism
- Cadherins/metabolism
- Zebrafish Proteins/metabolism
- Zebrafish/metabolism
- Mechanotransduction, Cellular*
- Endothelial Cells*/metabolism
- Vinculin*/metabolism
- Neovascularization, Physiologic
- Intercellular Junctions/metabolism
- Animals
 
- PubMed
- 35417696 Full text @ Cell Rep.
            Citation
        
        
            Kotini, M.P., van der Stoel, M.M., Yin, J., Han, M.K., Kirchmaier, B., de Rooij, J., Affolter, M., Huveneers, S., Belting, H.G. (2022) Vinculin controls endothelial cell junction dynamics during vascular lumen formation. Cell Reports. 39:110658.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Blood vessel morphogenesis is driven by coordinated endothelial cell behaviors. Active remodeling of cell-cell junctions promotes cellular plasticity while preserving vascular integrity. Here, we analyze the dynamics of endothelial adherens junctions during lumen formation in angiogenic sprouts in vivo. Live imaging in zebrafish reveals that lumen expansion is accompanied by the formation of transient finger-shaped junctions. Junctional fingers are positively regulated by blood pressure, whereas flow inhibition prevents their formation. Using fluorescent reporters, we show that junctional fingers contain the mechanotransduction protein vinculin. Furthermore, genetic deletion of vinculin prevents finger formation, a junctional defect that could be rescued by transient endothelial expression of vinculin. Our findings suggest a mechanism whereby lumen expansion leads to an increase in junctional tension, triggering recruitment of vinculin and formation of junctional fingers. We propose that endothelial cells employ force-dependent junctional remodeling to counteract external forces in order to maintain vascular integrity during sprouting angiogenesis.
            
    
        
        
    
    
    
                
                    
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