PUBLICATION
            tcf21+ epicardial cells adopt non-myocardial fates during zebrafish heart development and regeneration
- Authors
- Kikuchi, K., Gupta, V., Wang, J., Holdway, J.E., Wills, A.A., Fang, Y., and Poss, K.D.
- ID
- ZDB-PUB-110613-25
- Date
- 2011
- Source
- Development (Cambridge, England) 138(14): 2895-902 (Journal)
- Registered Authors
- Fang, Yi, Gupta, Vikas, Holdway, Jennifer, Kikuchi, Kazu, Poss, Kenneth D., Wang, Jinhu, Wills, Airon
- Keywords
- heart regeneration, heart development, cardiomyocyte, epicardium, zebrafish, genetic fate-mapping
- MeSH Terms
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                - Regeneration/genetics
- Regeneration/physiology*
- Cell Differentiation/physiology
- Cell Lineage/physiology
- Morphogenesis/genetics
- Morphogenesis/physiology*
- Fluorescent Antibody Technique
- Zebrafish Proteins/metabolism*
- Animals
- Zebrafish/embryology*
- Transcription Factors/metabolism*
- Pericardium/cytology*
- Pericardium/metabolism
- Gene Expression Regulation, Developmental/physiology*
- Heart/embryology*
- Animals, Genetically Modified
 
- PubMed
- 21653610 Full text @ Development
            Citation
        
        
            Kikuchi, K., Gupta, V., Wang, J., Holdway, J.E., Wills, A.A., Fang, Y., and Poss, K.D. (2011) tcf21+ epicardial cells adopt non-myocardial fates during zebrafish heart development and regeneration. Development (Cambridge, England). 138(14):2895-902.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Recent lineage-tracing studies have produced conflicting results about whether the epicardium is a source of cardiac muscle
                     cells during heart development. Here, we examined the developmental potential of epicardial tissue in zebrafish during both
                     embryonic development and injury-induced heart regeneration. We found that upstream sequences of the transcription factor
                     gene tcf21 activated robust, epicardium-specific expression throughout development and regeneration. Cre recombinase-based, genetic
                     fate-mapping of larval or adult tcf21+ cells revealed contributions to perivascular cells, but not cardiomyocytes, during each form of cardiogenesis. Our findings
                     indicate that natural epicardial fates are limited to non-myocardial cell types in zebrafish.
            
    
        
        
    
    
    
                
                    
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                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
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                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    