PUBLICATION
            Sema6a and Plxna2 mediate spatially regulated repulsion within the developing eye to promote eye vesicle cohesion
- Authors
 - Ebert, A.M., Childs, S.J., Hehr, C.L., Cechmanek, P.B., McFarlane, S.
 - ID
 - ZDB-PUB-140612-6
 - Date
 - 2014
 - Source
 - Development (Cambridge, England) 141: 2473-82 (Journal)
 - Registered Authors
 - Childs, Sarah J.
 - Keywords
 - Morphogenesis, Plexin, Repulsion, Semaphorin, Zebrafish
 - MeSH Terms
 - 
    
        
        
            
                
- Gene Expression Regulation, Developmental*
 - Zebrafish Proteins/genetics
 - Zebrafish Proteins/physiology*
 - Animals
 - Axons/metabolism
 - Semaphorins/genetics
 - Semaphorins/physiology*
 - Green Fluorescent Proteins/metabolism
 - Receptors, Cell Surface/genetics
 - Receptors, Cell Surface/physiology*
 - Morphogenesis
 - Signal Transduction
 - Gene Expression Profiling
 - Eye/embryology*
 - Cell Communication
 - Stem Cells/cytology
 - Zebrafish/embryology
 - Zebrafish/genetics
 - Nerve Tissue Proteins/genetics
 - Nerve Tissue Proteins/physiology*
 - Prosencephalon/embryology
 - Cell Proliferation
 - Cell Movement
 
 - PubMed
 - 24917502 Full text @ Development
 
            Citation
        
        
            Ebert, A.M., Childs, S.J., Hehr, C.L., Cechmanek, P.B., McFarlane, S. (2014) Sema6a and Plxna2 mediate spatially regulated repulsion within the developing eye to promote eye vesicle cohesion. Development (Cambridge, England). 141:2473-82.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Organs are generated from collections of cells that coalesce and remain together as they undergo a series of choreographed movements to give the organ its final shape. We know little about the cellular and molecular mechanisms that regulate tissue cohesion during morphogenesis. Extensive cell movements underlie eye development, starting with the eye field separating to form bilateral vesicles that go on to evaginate from the forebrain. What keeps eye cells together as they undergo morphogenesis and extensive proliferation is unknown. Here, we show that plexina2 (Plxna2), a member of a receptor family best known for its roles in axon and cell guidance, is required alongside the repellent semaphorin 6a (Sema6a) to keep cells integrated within the zebrafish eye vesicle epithelium. sema6a is expressed throughout the eye vesicle, whereas plxna2 is restricted to the ventral vesicle. Knockdown of Plxna2 or Sema6a results in a loss of vesicle integrity, with time-lapse microscopy showing that eye progenitors either fail to enter the evaginating vesicles or delaminate from the eye epithelium. Explant experiments, and rescue of eye vesicle integrity with simultaneous knockdown of sema6a and plxna2, point to an eye-autonomous requirement for Sema6a/Plxna2. We propose a novel, tissue-autonomous mechanism of organ cohesion, with neutralization of repulsion suggested as a means to promote interactions between cells within a tissue domain.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping