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Article
Microbeam radiation-induced tissue damage depends on the stage of vascular maturation
Faculty of Engineering and Information Sciences - Papers: Part A
  • Sara Sabatasso, University Of Fribourg
  • Jean Albert Laissue, University of Bern
  • Ruslun Hlushchuk, University Of Fribourg
  • Werner Graber, University of Bern
  • Alberto Bravin, European Synchrotron Radiation Facility
  • Elke Brauer-Krish, European Synchrotron Radiation Facility
  • Stéphanie Corde, European Synchrotron Radiation Facility
  • Hans Blattmann, University of Bern
  • Guenther Gruber, Radio Oncology Unit, Clinic Hirslanden
  • Valentin Djonov, University Of Fribourg
RIS ID
76635
Publication Date
1-1-2011
Publication Details

Sabatasso, S., Laissue, J. Albert., Hlushchuk, R., Graber, W., Bravin, A., Brauer-Krish, E., Corde, S., Blattmann, H., Gruber, G. & Djonov, V. (2011). Microbeam Radiation-Induced tissue damage depends on the stage of vascular maturation. International Journal of Radiation Oncology Biology Physics, 80 (5), 1522-1532.

Abstract
Purpose: To explore the effects of microbeam radiation (MR) on vascular biology, we used the chick chorioallantoic membrane (CAM) model of an almost pure vascular system with immature vessels (lacking periendothelial coverage) at Day 8 and mature vessels (with coverage) at Day 12 of development. Methods and Materials: CAMs were irradiated with microplanar beams (width, 25 mm; interbeam spacing, 200 mm) at entrance doses of 200 or 300 Gy and, for comparison, with a broad beam (seamless radiation [SLR]), with entrance doses of 5 to 40 Gy. Results: In vivo monitoring of Day-8 CAMvasculature 6 h after 200 GyMRrevealed a near total destruction of the immature capillary plexus. Conversely, 200 Gy MR barely affected Day-12 CAM mature microvasculature. Morphological evaluation of Day-12 CAMs after the dose was increased to 300 Gy revealed opened interendothelial junctions, which could explain the transient mesenchymal edema immediately after irradiation. Electron micrographs revealed cytoplasmic vacuolization of endothelial cells in the beam path, with disrupted luminal surfaces; often the lumen was engorged with erythrocytes and leukocytes. After 30 min, the capillary plexus adopted a striated metronomic pattern, with alternating destroyed and intact zones, corresponding to the beam and the interbeam paths within the array. SLR at a dose of 10 Gy caused growth retardation, resulting in a remarkable reduction in the vascular endpoint density 24 h postirradiation. A dose of 40 Gy damaged the entire CAM vasculature. Conclusions: The effects of MR are mediated by capillary damage, with tissue injury caused by insufficient blood supply. Vascular toxicity and physiological effects ofMRdepend on the stage of capillary maturation and appear in the first 15 to 60 min after irradiation. Conversely, the effects of SLR, due to the arrest of cell proliferation, persist for a longer time.
Citation Information
Sara Sabatasso, Jean Albert Laissue, Ruslun Hlushchuk, Werner Graber, et al.. "Microbeam radiation-induced tissue damage depends on the stage of vascular maturation" (2011)
Available at: http://works.bepress.com/stephanie_corde/19/