PUBLICATION
            Synapsin III Regulates Dopaminergic Neuron Development in Vertebrates
- Authors
 - Faustini, G., Longhena, F., Muscò, A., Bono, F., Parrella, E., La Via, L., Barbon, A., Pizzi, M., Onofri, F., Benfenati, F., Missale, C., Memo, M., Zizioli, D., Bellucci, A.
 - ID
 - ZDB-PUB-221212-1
 - Date
 - 2022
 - Source
 - Cells 11(23): (Journal)
 - Registered Authors
 - Keywords
 - attention deficit and hyperactivity disorder, dopaminergic neurons, neurodevelopment, synapsin III
 - MeSH Terms
 - 
    
        
        
            
                
- Animals
 - Mice, Knockout
 - Brain-Derived Neurotrophic Factor/genetics
 - Induced Pluripotent Stem Cells/metabolism
 - Humans
 - Zebrafish/metabolism
 - Dopaminergic Neurons*/metabolism
 - Methylphenidate/therapeutic use
 - Synapsins*/genetics
 - Synapsins*/metabolism
 - Dopamine
 - Mice
 
 - PubMed
 - 36497160 Full text @ Cells
 
            Citation
        
        
            Faustini, G., Longhena, F., Muscò, A., Bono, F., Parrella, E., La Via, L., Barbon, A., Pizzi, M., Onofri, F., Benfenati, F., Missale, C., Memo, M., Zizioli, D., Bellucci, A. (2022) Synapsin III Regulates Dopaminergic Neuron Development in Vertebrates. Cells. 11(23):.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Attention deficit and hyperactivity disorder (ADHD) is a neurodevelopmental disorder characterized by alterations in the mesocorticolimbic and nigrostriatal dopaminergic pathways. Polymorphisms in the Synapsin III (Syn III) gene can associate with ADHD onset and even affect the therapeutic response to the gold standard ADHD medication, methylphenidate (MPH), a monoamine transporter inhibitor whose efficacy appears related with the stimulation of brain-derived neurotrophic factor (BDNF). Interestingly, we previously showed that MPH can bind Syn III, which can regulate neuronal development. These observations suggest that Syn III polymorphism may impinge on ADHD onset and response to therapy by affecting BDNF-dependent dopaminergic neuron development. Here, by studying zebrafish embryos exposed to Syn III gene knock-down (KD), Syn III knock-out (ko) mice and human induced pluripotent stem cells (iPSCs)-derived neurons subjected to Syn III RNA interference, we found that Syn III governs the earliest stages of dopaminergic neurons development and that this function is conserved in vertebrates. We also observed that in mammals Syn III exerts this function acting upstream of brain-derived neurotrophic factor (BDNF)- and cAMP-dependent protein kinase 5 (Cdk5)-stimulated dendrite development. Collectively, these findings own significant implications for deciphering the biological basis of ADHD.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping