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   <subfield code="a">Low-dose irradiation causes rapid alterations to the proteome of the human endothelial cell line EA.hy926</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Franka Pluder, Zarko Barjaktarovic, Omid Azimzadeh, Simone Mörtl, Anne Krämer, Sylvia Steininger, Hakan Sarioglu, Dariusz Leszczynski, Reetta Nylund, Arvi Hakanen, Arundhathi Sriharshan, Michael Atkinson, Soile Tapio]</subfield>
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   <subfield code="a">High doses of ionising radiation damage the heart by an as yet unknown mechanism. A concern for radiological protection is the recent epidemiological data indicating that doses as low as 100-500mGy may induce cardiac damage. The aim of this study was to identify potential molecular targets and/or mechanisms involved in the pathogenesis of low-dose radiation-induced cardiovascular disease. The vascular endothelium plays a pivotal role in the regulation of cardiac function and is therefore a potential target tissue. We report here that low-dose radiation induced rapid and time-dependent changes in the cytoplasmic proteome of the human endothelial cell line EA.hy926. The proteomes were investigated at 4 and 24h after irradiation at two different dose rates (Co-60 gamma ray total dose 200mGy; 20mGy/min and 190mGy/min) using 2D-DIGE technology. Differentially expressed proteins were identified, after in-gel trypsin digestion, by MALDI-TOF/TOF tandem mass spectrometry, and peptide mass fingerprint analyses. We identified 15 significantly differentially expressed proteins, of which 10 were up-regulated and 5 down-regulated, with more than±1.5-fold difference compared with unexposed cells. Pathways influenced by the low-dose exposures included the Ran and RhoA pathways, fatty acid metabolism and stress response.</subfield>
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