PUBLICATION
            Definitive hematopoiesis initiates through a committed erythromyeloid progenitor in the zebrafish embryo
- Authors
 - Bertrand, J.Y., Kim, A.D., Violette, E.P., Stachura, D.L., Cisson, J.L., and Traver, D.
 - ID
 - ZDB-PUB-071029-11
 - Date
 - 2007
 - Source
 - Development (Cambridge, England) 134(23): 4147-4156 (Journal)
 - Registered Authors
 - Bertrand, Julien, Traver, David
 - Keywords
 - Erythromyeloid progenitor, Hematopoiesis, Hematopoietic progenitor cells, Zebrafish
 - MeSH Terms
 - 
    
        
        
            
                
- Embryo, Nonmammalian/cytology*
 - Embryo, Nonmammalian/physiology*
 - Flow Cytometry
 - Crosses, Genetic
 - Animals, Genetically Modified
 - Cell Transplantation
 - In Situ Hybridization, Fluorescence
 - Hematopoietic Stem Cells/cytology*
 - Zebrafish/embryology*
 - Zebrafish/genetics
 - Male
 - Embryonic Development
 - Reverse Transcriptase Polymerase Chain Reaction
 - Gene Expression Regulation, Developmental
 - Blood Cells/cytology
 - Blood Cells/physiology
 - Hematopoiesis/genetics
 - Hematopoiesis/physiology*
 - Erythroid Precursor Cells/cytology*
 - Female
 - Green Fluorescent Proteins/genetics
 - Animals
 
 - PubMed
 - 17959717 Full text @ Development
 
            Citation
        
        
            Bertrand, J.Y., Kim, A.D., Violette, E.P., Stachura, D.L., Cisson, J.L., and Traver, D. (2007) Definitive hematopoiesis initiates through a committed erythromyeloid progenitor in the zebrafish embryo. Development (Cambridge, England). 134(23):4147-4156.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Shifting sites of blood cell production during development is common across widely divergent phyla. In zebrafish, like other vertebrates, hematopoietic development has been roughly divided into two waves, termed primitive and definitive. Primitive hematopoiesis is characterized by the generation of embryonic erythrocytes in the intermediate cell mass and a distinct population of macrophages that arises from cephalic mesoderm. Based on previous gene expression studies, definitive hematopoiesis has been suggested to begin with the generation of presumptive hematopoietic stem cells (HSCs) along the dorsal aorta that express c-myb and runx1. Here we show, using a combination of gene expression analyses, prospective isolation approaches, transplantation, and in vivo lineage-tracing experiments, that definitive hematopoiesis initiates through committed erythromyeloid progenitors (EMPs) in the posterior blood island (PBI) that arise independently of HSCs. EMPs isolated by coexpression of fluorescent transgenes driven by the lmo2 and gata1 promoters exhibit an immature, blastic morphology and express only erythroid and myeloid genes. Transplanted EMPs home to the PBI, show limited proliferative potential, and do not seed subsequent hematopoietic sites such as the thymus or pronephros. In vivo fate-mapping studies similarly demonstrate that EMPs possess only transient proliferative potential, with differentiated progeny remaining largely within caudal hematopoietic tissue. Additional fate mapping of mesodermal derivatives in mid-somitogenesis embryos suggests that EMPs are born directly in the PBI. These studies provide phenotypic and functional analyses of the first hematopoietic progenitors in the zebrafish embryo and demonstrate that definitive hematopoiesis proceeds through two distinct waves during embryonic development.
            
    
        
        
    
    
    
                
                    
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                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping