PUBLICATION
            Dual role of Jam3b in early hematopoietic and vascular development
- Authors
 - Kobayashi, I., Kobayashi-Sun, J., Hirakawa, Y., Ouchi, M., Yasuda, K., Kamei, H., Fukuhara, S., Yamaguchi, M.
 - ID
 - ZDB-PUB-191220-3
 - Date
 - 2019
 - Source
 - Development (Cambridge, England) 147(1): (Journal)
 - Registered Authors
 - Fukuhara, Shigetomo, Kobayashi, Isao
 - Keywords
 - Hematopoietic stem cells, Junctional adhesion molecule, Mesoderm, Vascular endothelial cells, Zebrafish
 - MeSH Terms
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- Mesoderm/embryology
 - Receptors, Cell Surface/genetics
 - Receptors, Cell Surface/physiology*
 - Hematopoiesis*/physiology
 - Animals
 - Zebrafish Proteins/genetics
 - Zebrafish Proteins/metabolism
 - Zebrafish Proteins/physiology*
 - Cardiovascular System/cytology
 - Cardiovascular System/embryology*
 - Hematopoietic Stem Cells
 - MAP Kinase Signaling System
 - Endothelial Cells/physiology
 - Zebrafish
 - Basic Helix-Loop-Helix Transcription Factors/metabolism
 
 - PubMed
 - 31852685 Full text @ Development
 
            Citation
        
        
            Kobayashi, I., Kobayashi-Sun, J., Hirakawa, Y., Ouchi, M., Yasuda, K., Kamei, H., Fukuhara, S., Yamaguchi, M. (2019) Dual role of Jam3b in early hematopoietic and vascular development. Development (Cambridge, England). 147(1):.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                In order to efficiently derive hematopoietic stem cells (HSCs) from pluripotent precursors, it is crucial to understand how mesodermal cells acquire hematopoietic and endothelial identities, two divergent, but closely related cell fates. Although Npas4 has been recently identified as a conserved master regulator of hemato-vascular development, the molecular mechanisms underlying cell fate divergence between hematopoietic and vascular endothelial cells are still unclear. Here, we show in zebrafish that mesodermal cell differentiation into hematopoietic and vascular endothelial cells is regulated by Junctional adhesion molecule 3b (Jam3b) via two independent signaling pathways. Mutation of jam3b led to a reduction in npas4l expression in the posterior lateral plate mesoderm and defects in both hematopoietic and vascular development. Mechanistically, we uncover that Jam3b promotes endothelial specification by regulating npas4l expression through repression of the Rap1a-Erk signaling cascade. Jam3b subsequently promotes hematopoietic development, including HSCs, by regulating lrrc15 expression in endothelial precursors through the activation of an integrin-dependent signaling cascade. Our data provide insight into the divergent mechanisms for instructing hematopoietic or vascular fates from mesodermal cells.
            
    
        
        
    
    
    
                
                    
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