PUBLICATION
            Dynamic spatiotemporal coordination of neural stem cell fate decisions occurs through local feedback in the adult vertebrate brain
- Authors
- Dray, N., Mancini, L., Binshtok, U., Cheysson, F., Supatto, W., Mahou, P., Bedu, S., Ortica, S., Than-Trong, E., Krecsmarik, M., Herbert, S., Masson, J.B., Tinevez, J.Y., Lang, G., Beaurepaire, E., Sprinzak, D., Bally-Cuif, L.
- ID
- ZDB-PUB-210407-76
- Date
- 2021
- Source
- Cell Stem Cell 28(8): 1457-1472.e12 (Journal)
- Registered Authors
- Bally-Cuif, Laure
- Keywords
- Notch signaling, adult neural stem cell, analytical modeling, intrinsic niche, pallium, population behavior, quiescence, spatial statistics, spatiotemporal homeostasis, zebrafish
- MeSH Terms
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                - Neural Stem Cells*
- Neurogenesis*
- Animals
- Zebrafish
- Cell Proliferation
- Feedback
- Brain
 
- PubMed
- 33823144 Full text @ Cell Stem Cell
            Citation
        
        
            Dray, N., Mancini, L., Binshtok, U., Cheysson, F., Supatto, W., Mahou, P., Bedu, S., Ortica, S., Than-Trong, E., Krecsmarik, M., Herbert, S., Masson, J.B., Tinevez, J.Y., Lang, G., Beaurepaire, E., Sprinzak, D., Bally-Cuif, L. (2021) Dynamic spatiotemporal coordination of neural stem cell fate decisions occurs through local feedback in the adult vertebrate brain. Cell Stem Cell. 28(8):1457-1472.e12.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Neural stem cell (NSC) populations persist in the adult vertebrate brain over a lifetime, and their homeostasis is controlled at the population level through unknown mechanisms. Here, we combine dynamic imaging of entire NSC populations in their in vivo niche over several weeks with pharmacological manipulations, mathematical modeling, and spatial statistics and demonstrate that NSCs use spatiotemporally resolved local feedback signals to coordinate their decision to divide in adult zebrafish brains. These involve Notch-mediated short-range inhibition from transient neural progenitors and a dispersion effect from the dividing NSCs themselves exerted with a delay of 9-12 days. Simulations from a stochastic NSC lattice model capturing these interactions demonstrate that these signals are linked by lineage progression and control the spatiotemporal distribution of output neurons. These results highlight how local and temporally delayed interactions occurring between brain germinal cells generate self-propagating dynamics that maintain NSC population homeostasis and coordinate specific spatiotemporal correlations.
            
    
        
        
    
    
    
                
                    
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