PUBLICATION
            Perturbation of zebrafish swimbladder development by enhancing Wnt signaling in Wif1 morphants
- Authors
- Yin, A., Korzh, V., and Gong, Z.
- ID
- ZDB-PUB-111027-35
- Date
- 2012
- Source
- Biochimica et biophysica acta. Molecular cell research 1823(2): 236-244 (Journal)
- Registered Authors
- Gong, Zhiyuan, Korzh, Vladimir, Yin, Ao
- Keywords
- wnt signaling, wif1, swimbladder, hedgehog singaling, IWR-1, zebrafish
- MeSH Terms
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                - Oligonucleotides, Antisense/genetics
- Oligonucleotides, Antisense/metabolism
- Air Sacs/anatomy & histology
- Air Sacs/embryology*
- Air Sacs/metabolism
- Hedgehog Proteins/genetics
- Hedgehog Proteins/metabolism
- Gene Knockdown Techniques
- Wnt Signaling Pathway/physiology*
- Animals
- Zebrafish*/anatomy & histology
- Zebrafish*/embryology
- Cell Proliferation
- Adaptor Proteins, Signal Transducing/genetics
- Adaptor Proteins, Signal Transducing/metabolism*
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- Repressor Proteins/genetics
- Repressor Proteins/metabolism*
- Wnt Proteins/genetics
- Wnt Proteins/metabolism*
 
- PubMed
- 22008465 Full text @ BBA Molecular Cell Research
            Citation
        
        
            Yin, A., Korzh, V., and Gong, Z. (2012) Perturbation of zebrafish swimbladder development by enhancing Wnt signaling in Wif1 morphants. Biochimica et biophysica acta. Molecular cell research. 1823(2):236-244.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Wnt signaling plays critical roles in development of both tetrapod lung and fish swimbladder, which are the two evolutionary homologous organs. Our previous data reveal that down-regulation of Wnt signaling leads to defective swimbladder development. However, the effects of up-regulation of Wnt signaling on swimbladder development remain unclear. By knockdown of the Wnt protein inhibitory gene wif1, we demonstrated that up-regulation of Wnt signaling also resulted in perturbed development of the swimbladder. Specifically, the growth of epithelium and mesenchyme was greatly inhibited, the smooth muscle differentiation was abolished, and the organization of mesothelium was disturbed. Furthermore, our data reveal that it is the reduced cell proliferation, but not enhanced apoptosis, that contributes to the disturbance of swimbladder development in wif1 morphants. Blocking Wnt signaling by the Wnt antagonist IWR-1 did not affect wif1 expression in the swimbladder, but complete suppression of Hedgehog signaling in smo- / - mutants abolished wif expression, consistent with our earlier report of a negative feedback regulation of Wnt signaling in the swimbladder by the Hedgehog signaling. Our works established the importance of proper level of Wnt signaling for normal development of swimbladder in zebrafish.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    