PUBLICATION
            CXCR1 remodels the vascular niche to promote hematopoietic stem and progenitor cell engraftment
- Authors
- Blaser, B.W., Moore, J.L., Hagedorn, E.J., Li, B., Riquelme, R., Lichtig, A., Yang, S., Zhou, Y., Tamplin, O.J., Binder, V., Zon, L.I.
- ID
- ZDB-PUB-170330-3
- Date
- 2017
- Source
- The Journal of experimental medicine 214(4): 1011 (Journal)
- Registered Authors
- Moore, Jessica L., Tamplin, Owen, Zhou, Yi, Zon, Leonard I.
- Keywords
- none
- Datasets
- GEO:GSE92543, GEO:GSE56015, GEO:GSE92542
- MeSH Terms
- 
    
        
        
            
                - Receptors, Interleukin-8A/physiology*
- Cellular Microenvironment
- Zebrafish
- Interleukin-8/physiology
- Cells, Cultured
- Hematopoietic Stem Cells/physiology
- Hematopoietic Stem Cell Transplantation*
- Signal Transduction/physiology
- Animals
 
- PubMed
- 28351983 Full text @ J. Exp. Med.
            Citation
        
        
            Blaser, B.W., Moore, J.L., Hagedorn, E.J., Li, B., Riquelme, R., Lichtig, A., Yang, S., Zhou, Y., Tamplin, O.J., Binder, V., Zon, L.I. (2017) CXCR1 remodels the vascular niche to promote hematopoietic stem and progenitor cell engraftment. The Journal of experimental medicine. 214(4):1011.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The microenvironment is an important regulator of hematopoietic stem and progenitor cell (HSPC) biology. Recent advances marking fluorescent HSPCs have allowed exquisite visualization of HSPCs in the caudal hematopoietic tissue (CHT) of the developing zebrafish. Here, we show that the chemokine cxcl8 and its receptor, cxcr1, are expressed by zebrafish endothelial cells, and we identify cxcl8/cxcr1 signaling as a positive regulator of HSPC colonization. Single-cell tracking experiments demonstrated that this is a result of increases in HSPC-endothelial cell "cuddling," HSPC residency time within the CHT, and HSPC mitotic rate. Enhanced cxcl8/cxcr1 signaling was associated with an increase in the volume of the CHT and induction of cxcl12a expression. Finally, using parabiotic zebrafish, we show that cxcr1 acts HSPC nonautonomously to improve the efficiency of donor HSPC engraftment. This work identifies a mechanism by which the hematopoietic niche remodels to promote HSPC engraftment and suggests that cxcl8/cxcr1 signaling is a potential therapeutic target in patients undergoing hematopoietic stem cell transplantation.
            
    
        
        
    
    
    
                
                    
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                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
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