PUBLICATION
            Stable multilineage xenogeneic replacement of definitive hematopoiesis in adult zebrafish
- Authors
- Hess, I., Boehm, T.
- ID
- ZDB-PUB-160119-6
- Date
- 2016
- Source
- Scientific Reports 6: 19634 (Journal)
- Registered Authors
- Boehm, Tom, Hess, Isabell
- Keywords
- Lymphopoiesis, Medical research
- MeSH Terms
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                - Hematopoietic Stem Cell Transplantation
- Zebrafish Proteins/genetics*
- Heterografts
- Animals
- Proto-Oncogene Proteins c-myc/genetics
- Cell Differentiation
- Zebrafish/genetics*
- Hematopoietic Stem Cells/cytology
- Hematopoietic Stem Cells/metabolism
- Mutation
- Hematopoiesis/genetics*
 
- PubMed
- 26777855 Full text @ Sci. Rep.
            Citation
        
        
            Hess, I., Boehm, T. (2016) Stable multilineage xenogeneic replacement of definitive hematopoiesis in adult zebrafish. Scientific Reports. 6:19634.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Bony fishes are the most numerous and phenotypically diverse group of vertebrates inhabiting our planet, making them an ideal target for identifying general principles of tissue development and function. However, lack of suitable experimental platforms prevents the exploitation of this rich source of natural phenotypic variation. Here, we use a zebrafish strain lacking definitive hematopoiesis for interspecific analysis of hematopoietic cell development. Without conditioning prior to transplantation, hematopoietic progenitor cells from goldfish stably engraft in adult zebrafish homozygous for the c-myb(I181N) mutation. However, in competitive repopulation experiments, zebrafish hematopoietic cells exhibit an advantage over their goldfish counterparts, possibly owing to subtle species-specific functional differences in hematopoietic microenvironments resulting from over 100 million years of independent evolution. Thus, our unique animal model provides an unprecedented opportunity to genetically and functionally disentangle universal and species-specific contributions of the microenvironment to hematopoietic progenitor cell maintenance and development.
            
    
        
        
    
    
    
                
                    
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                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    