PUBLICATION
            Asymmetric involution of the myocardial field drives heart tube formation in zebrafish
- Authors
- Rohr, S., Otten, C., and Abdelilah-Seyfried, S.
- ID
- ZDB-PUB-080218-11
- Date
- 2008
- Source
- Circulation research 102(2): e12-19 (Journal)
- Registered Authors
- Abdelilah-Seyfried, Salim
- Keywords
- heart tube, cell polarity, protein kinase C iota, left–right asymmetry, southpaw, nagie oko
- MeSH Terms
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                - Epithelial Cells
- Embryo, Nonmammalian
- Heart/embryology*
- Heart/growth & development
- Myocardium/cytology
- Zebrafish
- Animals
- Cell Movement
- Gene Expression Regulation, Developmental*
- Morphogenesis*
 
- PubMed
- 18202314 Full text @ Circ. Res.
            Citation
        
        
            Rohr, S., Otten, C., and Abdelilah-Seyfried, S. (2008) Asymmetric involution of the myocardial field drives heart tube formation in zebrafish. Circulation research. 102(2):e12-19.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Many vertebrate organs are derived from monolayered epithelia that undergo morphogenesis to acquire their shape. Whereas asymmetric left/right gene expression within the zebrafish heart field has been well documented, little is known about the tissue movements and cellular changes underlying early cardiac morphogenesis. Here, we demonstrate that asymmetric involution of the myocardium of the right-posterior heart field generates the ventral floor, whereas the noninvoluting left heart field gives rise to the dorsal roof of the primary heart tube. During heart tube formation, asymmetric left/right gene expression within the myocardium correlates with asymmetric tissue morphogenesis. Disruption of left/right gene expression causes randomized myocardial tissue involution. Time-lapse analysis combined with genetic analyses reveals that motility of the myocardial epithelium is a tissue migration process. Our results demonstrate that asymmetric morphogenetic movements of the 2 bilateral myocardial cell populations generate different dorsoventral regions of the zebrafish heart tube. Failure to generate a heart tube does not affect the acquisition of atrial versus ventricular cardiac cell shapes. Therefore, establishment of basic cardiac cell shapes precedes cardiac function. Together, these results provide the framework for the integration of single cell behaviors during the formation of the vertebrate primary heart tube.
            
    
        
        
    
    
    
                
                    
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                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
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