PUBLICATION
            Zebrafish fin regeneration involves transient serotonin synthesis
- Authors
 - König, D., Jaźwińska, A.
 - ID
 - ZDB-PUB-190425-18
 - Date
 - 2019
 - Source
 - Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society 27(4): 375-385 (Journal)
 - Registered Authors
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Zebrafish/physiology*
 - Signal Transduction
 - Animal Fins/blood supply
 - Animal Fins/physiology*
 - Cell Differentiation
 - Animals
 - Serotonin/biosynthesis*
 - Wound Healing/physiology
 - Gene Expression Regulation, Developmental/drug effects
 - Regeneration/physiology*
 - Cell Proliferation
 - Fibroblast Growth Factors/metabolism
 - Amputation Stumps*/blood supply
 
 - PubMed
 - 31017740 Full text @ Wound Repair Regen.
 
            Citation
        
        
            König, D., Jaźwińska, A. (2019) Zebrafish fin regeneration involves transient serotonin synthesis. Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society. 27(4):375-385.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The zebrafish is a vertebrate organism capable of regenerating many of its organs. Notably, it can undergo epimorphic regeneration of its fins after amputation. This process occurs through the formation of a wound epithelium and the dedifferentiation of mesenchymal and bone-forming cells, which form a proliferative blastema. Here, we report that the entry into the regenerative process involves the local synthesis of serotonin (5-hydroxytryptamine, 5-HT) in the injury-associated tissue. One day after wounding, intracellular accumulation of serotonin was induced in the stump below the amputation plane. During blastema formation, serotonin was detected in the mesenchyme at the vicinity of the amputation plane and in the apical wound epithelium. During the advanced outgrowth phase, this monoamine was no longer present in the blastema, suggesting a temporal involvement of serotonin in the postinjury area. We show the expression of two serotonin synthesizing enzymes, tryptophan hydroxylase 1a and 1b in the blastema, suggesting the local production of this monoamine. Neither depletion of serotonin by chemical inhibition of tryptophan hydroxylase, nor ectopic administration of this monoamine affected fin regeneration, indicating it does not play a role during this process. Finally, we found that the presence of serotonin during regeneration depends on fibroblast growth factor and retinoic acid signaling. Overall, our study demonstrates that the initiation of fin regeneration is associated with a transient synthesis of serotonin in the regrowing tissue.
            
    
        
        
    
    
    
                
                    
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