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    Integrative proteomic and microRNA analysis of primary human coronary artery endothelial cells exposed to low-dose gamma radiation.
        
        Radiat. Environ. Biophys. 52, 87-98 (2013)
    
    
    
				High doses of ionising radiation significantly increase the risk of cardiovascular disease (CVD), the vascular endothelium representing one of the main targets. Whether radiation doses lower than 500 mGy induce cardiovascular damage is controversial. The aim of this study was to investigate radiation-induced expression changes on protein and microRNA (miRNA) level in primary human coronary artery endothelial cells after a single 200 mGy radiation dose (Co-60). Using a multiplex gel-based proteomics technology (2D-DIGE), we identified 28 deregulated proteins showing more than ±1.5-fold expression change in comparison with non-exposed cells. A great majority of the proteins showed up-regulation. Bioinformatics analysis indicated "cellular assembly and organisation, cellular function and maintenance and molecular transport" as the most significant radiation-responsive network. Caspase-3, a central regulator of this network, was confirmed to be up-regulated using immunoblotting. We also analysed radiation-induced alterations in the level of six miRNAs known to play a role either in CVD or in radiation response. The expression of miR-21 and miR-146b showed significant radiation-induced deregulation. Using miRNA target prediction, three proteins found differentially expressed in this study were identified as putative candidates for miR-21 regulation. A negative correlation was observed between miR-21 levels and the predicted target proteins, desmoglein 1, phosphoglucomutase and target of Myb protein. This study shows for the first time that a low-dose exposure has a significant impact on miRNA expression that is directly related to protein expression alterations. The data presented here may facilitate the discovery of low-dose biomarkers of radiation-induced cardiovascular damage.
			
			
		Impact Factor
					Scopus SNIP
					Web of Science
Times Cited
					Times Cited
Scopus
Cited By
					
					Cited By
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				1.754
					1.004
					31
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
    
        Schlagwörter
        Ionising Radiation ; Proteomics ; Low-dose Radiation ; Mir-21 ; Mir-146b ; Endothelium ; Radiation-induced Cardiovascular Disease; Ionizing-radiation ; Cardiovascular-disease ; Long-term ; Mortality Experience ; Polyacrylamide-gels ; Statistical-model ; Breast-cancer ; Heart-disease ; Follow-up ; Mayak Pa
    
 
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2013
    
 
     
    
        HGF-Berichtsjahr
        2013
    
 
    
    
        ISSN (print) / ISBN
        0301-634X
    
 
    
        e-ISSN
        1432-2099
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        Radiation and Environmental Biophysics
    
 
		
    
        Quellenangaben
        
	    Band: 52,  
	    Heft: 1,  
	    Seiten: 87-98 
	    
	    
	
    
 
  
         
        
            Verlag
            Springer
        
 
         
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institute of Radiation Biology (ISB)
CF Metabolomics & Proteomics (CF-MPC)
Translational Metabolic Oncology (IDC-TMO)
 
    CF Metabolomics & Proteomics (CF-MPC)
Translational Metabolic Oncology (IDC-TMO)
        POF Topic(s)
        30202 - Environmental Health
30203 - Molecular Targets and Therapies
 
    30203 - Molecular Targets and Therapies
        Forschungsfeld(er)
        Radiation Sciences
Enabling and Novel Technologies
 
    Enabling and Novel Technologies
        PSP-Element(e)
        G-500200-001
G-505700-001
G-501000-001
 
     
     	
    G-505700-001
G-501000-001
        PubMed ID
        23138885
    
    
    
        WOS ID
        WOS:000315385100009
    
    
        Scopus ID
        84874389322
    
    
        Erfassungsdatum
        2013-03-01