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    Increased radial glia quiescence, decreased reactivation upon injury and unaltered neuroblast behavior underlie decreased neurogenesis in the aging zebrafish telencephalon.
        
        J. Comp. Neurol. 521, 3099-3115 (2013)
    
    
    
				The zebrafish has recently become a source of new data on the mechanisms of neural stem cell (NSC) maintenance and ongoing neurogenesis in adult brains. In this vertebrate, neurogenesis occurs at high levels in all ventricular regions of the brain, and brain injuries recover successfully, owing to the recruitment of radial glia, which function as NSCs. This new vertebrate model of adult neurogenesis is thus advancing our knowledge of the molecular cues in use for the activation of NSCs and fate of their progeny. Because the regenerative potential of somatic stem cells generally weakens with increasing age, it is important to assess the extent to which zebrafish NSC potential decreases or remains unaltered with age. We found that neurogenesis in the ventricular zone, in the olfactory bulb, and in a newly identified parenchymal zone of the telencephalon indeed declines as the fish ages and that oligodendrogenesis also declines. In the ventricular zone, the radial glial cell population remains largely unaltered morphologically but enters less frequently into the cell cycle and hence produces fewer neuroblasts. The neuroblasts themselves do not change their behavior with age and produce the same number of postmitotic neurons. Thus, decreased neurogenesis in the physiologically aging zebrafish brain is correlated with an increasing quiescence of radial glia. After injuries, radial glia in aged brains are reactivated, and the percentage of cell cycle entry is increased in the radial glia population. However, this reaction is far less pronounced than in younger animals, pointing to irreversible changes in aging zebrafish radial glia.
			
			
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Times Cited
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
    
        Schlagwörter
        S100β; adult neurogenesis; aging; deltaA; gfap; injury; neural stem cells; quiescence; radial glia; regeneration; telencephalon; zebrafish; Neural Stem-cells ; Adult Hippocampal Neurogenesis ; Age-related Decline ; Subventricular Zone ; Ventricular Zone ; Dentate Gyrus ; Brain ; Proliferation ; Expression ; Progenitors
    
 
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2013
    
 
     
    
        HGF-Berichtsjahr
        2013
    
 
    
    
        ISSN (print) / ISBN
        0021-9967
    
 
    
        e-ISSN
        1096-9861
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        Journal of Comparative Neurology, The
    
 
		
    
        Quellenangaben
        
	    Band: 521,  
	    Heft: 13,  
	    Seiten: 3099-3115 
	    
	    
	
    
 
  
         
        
            Verlag
            Wiley
        
 
         
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Research Unit Sensory Biology and Organogenesis (SBO)
Institute of Stem Cell Research (ISF)
 
    Institute of Stem Cell Research (ISF)
        POF Topic(s)
        30204 - Cell Programming and Repair
    
 
    
        Forschungsfeld(er)
        Stem Cell and Neuroscience
    
 
    
        PSP-Element(e)
        G-500100-001
G-500800-001
 
     
     	
    G-500800-001
        PubMed ID
        23787922
    
    
    
        WOS ID
        WOS:000321865200013
    
    
        Scopus ID
        84880646091
    
    
        Erfassungsdatum
        2013-08-02