PUBLICATION
            Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis
- Authors
- Kramer-Zucker, A.G., Olale, F., Haycraft, C.J., Yoder, B.K., Schier, A.F., and Drummond, I.A.
- ID
- ZDB-PUB-050328-4
- Date
- 2005
- Source
- Development (Cambridge, England) 132(8): 1907-1921 (Journal)
- Registered Authors
- Drummond, Iain, Kramer-Zucker, Albrecht, Olale, Felix, Schier, Alexander
- Keywords
- Cilia, Pronephros, Kupffer's vesicle, Ependymal cell, Spinal canal, Kidney cyst, Hydrocephalus, Left-right asymmetry
- MeSH Terms
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                - In Situ Hybridization
- Microscopy, Electron
- Organogenesis/physiology*
- Microscopy, Video
- Body Patterning/physiology
- Base Sequence
- Organizers, Embryonic/embryology*
- Animals
- DNA Primers
- Nerve Tissue Proteins/genetics
- Body Fluids/physiology*
- Dyneins/genetics
- Microscopy, Fluorescence
- Sequence Analysis, DNA
- Immunohistochemistry
- Cloning, Molecular
- Oligonucleotides
- Embryo, Nonmammalian/embryology
- Embryo, Nonmammalian/ultrastructure
- Kidney/embryology*
- Cilia/physiology*
- Central Nervous System/embryology*
- Molecular Sequence Data
- Zebrafish/embryology*
 
- PubMed
- 15790966 Full text @ Development
            Citation
        
        
            Kramer-Zucker, A.G., Olale, F., Haycraft, C.J., Yoder, B.K., Schier, A.F., and Drummond, I.A. (2005) Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis. Development (Cambridge, England). 132(8):1907-1921.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Cilia, as motile and sensory organelles, have been implicated in normal development, as well as diseases including cystic kidney disease, hydrocephalus and situs inversus. In kidney epithelia, cilia are proposed to be non-motile sensory organelles, while in the mouse node, two cilia populations, motile and non-motile have been proposed to regulate situs. We show that cilia in the zebrafish larval kidney, the spinal cord and Kupffer's vesicle are motile, suggesting that fluid flow is a common feature of each of these organs. Disruption of cilia structure or motility resulted in pronephric cyst formation, hydrocephalus and left-right asymmetry defects. The data show that loss of fluid flow leads to fluid accumulation, which can account for organ distension pathologies in the kidney and brain. In Kupffer's vesicle, loss of flow is associated with loss of left-right patterning, indicating that the `nodal flow' mechanism of generating situs is conserved in non-mammalian vertebrates.
            
    
        
        
    
    
    
                
                    
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                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
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