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Late proliferating and inflammatory effects on murine microvascular heart and lung endothelial cells after irradiation.
Radiother. Oncol. 117, 376-381 (2015)
BACKGROUND AND PURPOSE: Radiotherapy of thoracic tumors increases the risk to develop cardiac diseases at later time-points. We compared time kinetics of radiation-induced changes of surface markers related to proliferation, progenitor cell development and inflammation in lung and heart microvascular endothelial cells (ECs). MATERIAL AND METHODS: Mice received local thorax irradiation with a single dose of 0, 2 or 8Gy. Following magnetic bead separation and biotin-streptavidin competition, cell surface markers of isolated ECs from the lung and heart were analyzed 5, 10, 15 and 20weeks after irradiation by flow cytometry. RESULTS: Irradiation with 8Gy resulted in a temporary and differential up-regulation of proliferation markers (HCAM, Integrin β-3, Endoglin, VE-cadherin, VEGFR-2) on ECs. Mucosialin a progenitor marker increased in lung ECs 15-20weeks and inflammatory markers (PECAM-1, ICAM-1, ICAM-2, VCAM-1) started to increase 10weeks after thorax irradiation with 8Gy. Interestingly, ICAM-1 and VCAM-1 remained up-regulated 20weeks after irradiation in heart and lung ECs. CONCLUSIONS: The persistently elevated expression density of ICAM-1 and VCAM-1 on ECs may suggest that an irradiation at 8Gy induces late inflammatory responses in heart and lung ECs.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Scopus
Cited By
Cited By
Altmetric
4.363
1.703
33
34
Anmerkungen
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Atherosclerosis ; Endothelial Cells ; Endothelial Progenitor Cells ; Inflammation ; Irradiation ; Proliferation; C57bl/6 Wild-type; Adhesion Molecules; Radiation; Atherosclerosis; Mechanisms; Disease; Damage; Mice; Expression; Vcam-1
Sprache
englisch
Veröffentlichungsjahr
2015
HGF-Berichtsjahr
2015
ISSN (print) / ISBN
0167-8140
e-ISSN
1879-0887
Zeitschrift
Radiotherapy and Oncology
Quellenangaben
Band: 117,
Heft: 2,
Seiten: 376-381
Verlag
Elsevier
Verlagsort
Clare
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Radiation Medicine (IRM)
Translational Metabolic Oncology (IDC-TMO)
Institute of Radiation Biology (ISB)
Translational Metabolic Oncology (IDC-TMO)
Institute of Radiation Biology (ISB)
POF Topic(s)
30203 - Molecular Targets and Therapies
30202 - Environmental Health
30202 - Environmental Health
Forschungsfeld(er)
Radiation Sciences
PSP-Element(e)
G-501390-001
G-501000-001
G-500200-001
G-501000-001
G-500200-001
PubMed ID
26233589
WOS ID
WOS:000370460400029
Scopus ID
84952637542
Scopus ID
84938099933
Erfassungsdatum
2015-08-05