PUBLICATION
            Delta-Notch signalling controls commitment to a secretory fate in the zebrafish intestine
- Authors
- Crosnier, C., Vargesson, N., Gschmeissner, S., Ariza-McNaughton, L., Morrison, A., and Lewis, J.
- ID
- ZDB-PUB-050209-3
- Date
- 2005
- Source
- Development (Cambridge, England) 132(5): 1093-1104 (Journal)
- Registered Authors
- Lewis, Julian
- Keywords
- Intestine, DeltaD, DeltaC, Notch, mind bomb, Zebrafish, Monoclonal antibody, Stem cells, Goblet cells, Enteroendocrine cells, Absorptive cells
- MeSH Terms
- 
    
        
        
            
                - RNA/metabolism
- Intracellular Signaling Peptides and Proteins
- Antibodies, Monoclonal/metabolism
- Ligands
- Phenotype
- Signal Transduction*
- Gene Expression Regulation, Developmental*
- Mutation
- In Situ Nick-End Labeling
- Intestines/embryology*
- Intestines/metabolism*
- Receptors, Notch
- Animals
- Cell Movement
- Cell Lineage
- Zebrafish
- Cell Differentiation
- Cell Proliferation
- Blotting, Western
- Reverse Transcriptase Polymerase Chain Reaction
- Membrane Proteins/metabolism*
 
- PubMed
- 15689380 Full text @ Development
            Citation
        
        
            Crosnier, C., Vargesson, N., Gschmeissner, S., Ariza-McNaughton, L., Morrison, A., and Lewis, J. (2005) Delta-Notch signalling controls commitment to a secretory fate in the zebrafish intestine. Development (Cambridge, England). 132(5):1093-1104.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The transparency of the juvenile zebrafish and its genetic advantages make it an attractive model for study of cell turnover in the gut. BrdU labelling shows that the gut epithelium is renewed in essentially the same way as in mammals: the villi are lined with non-dividing differentiated cells, while cell division is confined to the intervillus pockets. New cells produced in the pockets take about 4 days to migrate out to the tips of the villi, where they die. We have generated monoclonal antibodies to identify the absorptive and secretory cells in the epithelium, and we have used these antibodies to examine the part that Delta-Notch signalling plays in producing the diversity of intestinal cell types. Several Notch receptors and ligands are expressed in the gut. In particular, the Notch ligand DeltaD (Delta1 in the mouse) is expressed in cells of the secretory lineage. In an aei mutant, where DeltaD is defective, secretory cells are overproduced. In mind bomb (mib), where all Delta-Notch signalling is believed to be blocked, almost all the cells in the 3-day gut epithelium adopt a secretory character. Thus, secretory differentiation appears to be the default in the absence of Notch activation, and lateral inhibition mediated by Delta-Notch signalling is required to generate a balanced mixture of absorptive and secretory cells. These findings demonstrate the central role of Notch signalling in the gut stem-cell system and establish the zebrafish as a model for study of the mechanisms controlling renewal of gut epithelium.
            
    
        
        
    
    
    
                
                    
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                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    