möglich sobald  bei der ZB eingereicht worden ist.
		
    Shaping of terminal megakaryocyte differentiation and proplatelet development by sphingosine-1-phosphate receptor S1P4.
        
        FASEB J. 24, 4701-4710 (2010)
    
    
    
				Megakaryocytes, which mature from hematopoietic progenitors in the bone marrow, further differentiate by reorganizing their cytoplasm into long proplatelet extensions that release platelets into the circulation. The molecular mechanisms underlying this highly dynamic cytoplasmic and cytoskeletal remodeling process are only poorly understood. Here we report that sphingosine 1-phosphate receptor 4 (S1P(4)) is specifically up-regulated during the development of human megakaryocytes from progenitor cells and is expressed in mature murine megakaryocytes. Megakaryocytes generated from S1P(4)-deficient murine bone marrow showed atypical and reduced formation of proplatelets in vitro. The recovery of platelet numbers after experimental thrombocytopenia was significantly delayed in S1p4(-/-) mice. Remarkably, overexpression and stimulation of S1P(4) in human erythroleukemia HEL cells promoted endomitosis, formation of cytoplasmic extensions, and subsequent release of platelet-like particles. These observations indicate that S1P(4) is involved in shaping the terminal differentiation of megakaryocytes.-Golfier, S., Kondo, S., Schulze, T., Takeuchi, T., Vassileva, G., Achtman, A. H., Gräler, M. H., Abbondanzo, S. J., Wiekowski, M., Kremmer, E., Endo, Y., Lira, S. A., Bacon, K. B., Lipp, M. Shaping of terminal megakaryocyte differentiation and proplatelet development by sphingosine-1-phosphate receptor S1P(4).
			
			
		Impact Factor
					Scopus SNIP
					Web of Science
Times Cited
					Times Cited
Scopus
Cited By
					
					Cited By
Altmetric
					
				6.401
					1.550
					33
					59
					
					
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
    
        Schlagwörter
        Platelets; Lysophospholipids; Receptor-deficient mice
    
 
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2010
    
 
     
    
        HGF-Berichtsjahr
        2010
    
 
    
    
        ISSN (print) / ISBN
        0892-6638
    
 
    
        e-ISSN
        1530-6860
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        FASEB Journal
    
 
		
    
        Quellenangaben
        
	    Band: 24,  
	    Heft: 12,  
	    Seiten: 4701-4710 
	    
	    
	
    
 
  
         
        
            Verlag
            Wiley
        
 
        
            Verlagsort
            Bethesda, Md.
        
 
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institute of Molecular Immunology (IMI)
    
 
     
     
    
        PSP-Element(e)
        G-501700-003
    
 
     
     	
    
        PubMed ID
        20686109
    
    
    
        Scopus ID
        78649740029
    
    
        Erfassungsdatum
        2010-12-13