PUBLICATION
            Characterization of neural stem cells and their progeny in the adult zebrafish optic tectum
- Authors
- Ito, Y., Tanaka, H., Okamoto, H., and Ohshima, T.
- ID
- ZDB-PUB-100330-35
- Date
- 2010
- Source
- Developmental Biology 342(1): 26-38 (Journal)
- Registered Authors
- Okamoto, Hitoshi, Tanaka, Hideomi
- Keywords
- Adult neurogenesis, Neural stem cells, Optic tectum, Radial glia, Zebrafish
- MeSH Terms
- 
    
        
        
            
                - Adult
- Humans
- Neurons/cytology
- Neurons/metabolism*
- Animals, Genetically Modified
- Multipotent Stem Cells/metabolism
- Zebrafish/genetics
- Zebrafish/metabolism
- Bromodeoxyuridine/metabolism
- Animals
- Brain/cytology
- Brain/metabolism*
- Stem Cells/cytology
- Stem Cells/metabolism*
- Stem Cells/physiology
- Superior Colliculi/metabolism*
- Green Fluorescent Proteins/genetics
- Green Fluorescent Proteins/metabolism
- Cell Differentiation/genetics
- Cell Differentiation/physiology
- Neuroglia/cytology
- Neuroglia/metabolism*
- Glial Fibrillary Acidic Protein/genetics
- Glial Fibrillary Acidic Protein/metabolism
 
- PubMed
- 20346355 Full text @ Dev. Biol.
            Citation
        
        
            Ito, Y., Tanaka, H., Okamoto, H., and Ohshima, T. (2010) Characterization of neural stem cells and their progeny in the adult zebrafish optic tectum. Developmental Biology. 342(1):26-38.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                In the adult teleost brain, proliferating cells are observed in a broad area, while these cells have a restricted distribution in adult mammalian brains. In the adult teleost optic tectum, most of the proliferating cells are distributed in the caudal margin of the periventricular gray zone (PGZ). We found that the PGZ is largely divided into 3 regions: 1 mitotic region and 2 post-mitotic regions-the superficial and deep layers. These regions are distinguished by the differential expression of several marker genes: pcna, sox2, msi1, elavl3, gfap, fabp7a, and s100beta. Using transgenic zebrafish Tg (gfap:GFP), we found that the deep layer cells specifically express gfap:GFP and have a radial glial morphology. We noted that bromodeoxyuridine (BrdU)-positive cells in the mitotic region did not exhibit glial properties, but maintained neuroepithelial characteristics. Pulse-chase experiments with BrdU-positive cells revealed the presence of self-renewing stem cells within the mitotic region. BrdU-positive cells differentiate into glutamatergic or GABAergic neurons and oligodendrocytes in the superficial layer and into radial glial cells in the deep layer. These results demonstrate that the proliferating cells in the PGZ contribute to neuronal and glial lineages to maintain the structure of the optic tectum in adult zebrafish.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    