PUBLICATION
            CFTR regulates embryonic T lymphopoiesis via Wnt signaling in zebrafish
- Authors
 - Lin, Z., Luo, M., Zhou, B., Liu, Y., Sun, H.
 - ID
 - ZDB-PUB-210506-7
 - Date
 - 2021
 - Source
 - Immunology Letters 234: 47-53 (Journal)
 - Registered Authors
 - Sun, Huaqin
 - Keywords
 - CFTR, T lymphopoiesis, Wnt signaling, Zebrafish
 - MeSH Terms
 - 
    
        
        
            
                
- Computational Biology/methods
 - Hematopoietic Stem Cells/cytology
 - Hematopoietic Stem Cells/metabolism
 - Cystic Fibrosis Transmembrane Conductance Regulator/genetics
 - Cystic Fibrosis Transmembrane Conductance Regulator/metabolism
 - Gene Expression Profiling
 - Gene Expression Regulation, Developmental*
 - Cell Differentiation/genetics*
 - Disease Models, Animal
 - Zebrafish
 - Animals
 - Mutation
 - T-Lymphocytes/cytology*
 - T-Lymphocytes/metabolism*
 - Lymphopoiesis/genetics*
 - Gene Ontology
 - Phenotype
 - Wnt Signaling Pathway*
 
 - PubMed
 - 33951474 Full text @ Immunol. Lett.
 
            Citation
        
        
            Lin, Z., Luo, M., Zhou, B., Liu, Y., Sun, H. (2021) CFTR regulates embryonic T lymphopoiesis via Wnt signaling in zebrafish. Immunology Letters. 234:47-53.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The number and function of T cells are abnormal as observed in cystic fibrosis (CF) patients and CF mouse models, and our previous work shows that the CFTR mutant leads to deficiency of primitive and definitive hematopoietic in zebrafish. However, the functions and underlying mechanisms of CFTR in T cell development during early embryogenesis have not been explored. Here, we report that the genetic ablation of CFTR in zebrafish resulted in abrogated embryonic T lymphopoiesis, which was ascribed to impaired thymic homing and expansion of hematopoietic stem cells (HSCs). Transcriptome analysis of isolated HSCs in zebrafish embryos at 48 hpf showed a significant alteration of key factors essential for T cell development and Wnt signaling, consistent with our previous work on CFTR regulating hematopoiesis. In brief, we uncovered the function of CFTR in embryonic T cell development and suggest that the immune deficiency of CF patients may originate from an early embryonic stage.
            
    
        
        
    
    
    
                
                    
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                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
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