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Regional differences in the response of neural stem cells and their microenvironment to ionizing radiation

Abstract
Radiation therapy is one of the most effective tools for treating malignant tumors; however, cranial irradiation often results in intellectual impairment and cognitive deficits, such as impaired learning and memory. Ionizing radiation generates DNA damage, causing proliferative cells to undergo apoptosis. In most brain regions, the generation of neurons is complete at birth. However, in two discrete regions, the granule cell layer of the hippocampus and the subventricular zone (SVZ) of the lateral ventricle, stem cell continuously proliferate and generate new neurons throughout life. Due to their high proliferative capacity, these cells are particularly vulnerable to ionizing radiation. The studies in this thesis focused on the immediate and late effects of ionizing radiation on neural stem cells and their microenvironment. We found that a single dose of 6 Gy at postnatal day 9 leads to long-lasting decreases in both stem cell proliferation, as well as neurogenesis, in the adult rat. Even though the two stem cell regions were equally affected by the initial radiation, there was a differential response in stem cell recovery. While hippocampal stem cells were long-term affected; SVZ stem cells seemed to recover with time. In addition, the radiation injury caused an immediate inflammatory response in the postnatal brain, which was not sustained into adulthood. Interestingly, irradiated microglia in the SVZ, but not hippocampus, upregulated several genes coding for growth factors known to promote stem cell maintenance, proliferation and survival. The specific upregulation of these stem cell-related genes in irradiated SVZ microglia could potentially contribute to the recovery of the stem cell population seen in the SVZ, which was lacking in the hippocampus. Taken together, these data demonstrate the pronounced susceptibility of hippocampal stem cells to ionizing radiation, and highlight the importance of shielding this structure from irradiation to minimize functional consequences.
Parts of work
I. Hellström NA, Zachrisson O, Kuhn HG and Patrone C. Rapid quantification of neurons and stem/progenitor cells in the adult mouse brain by flow cytometry. Letters in drug design and discovery (2007) 4:532-539
 
II. Hellström NA, Björk-Eriksson T, Blomgren K and Kuhn HG. Differential recovery of neural stem cells in the subventricular zone and dentate gyrus after ionizing radiation. Stem Cells (2009) 27:634-641 ::pmid::19056908
 
III. Hellström NA, Ståhlberg A, Swanpalmer J, Björk-Eriksson T, Blomgren K and Kuhn HG. Unique gene expression patterns indicate microglial contribution to neural stem cell recovery following irradiation. Unpublished manuscript
 
Degree
Doctor of Philosophy (Medicine)
University
University of Gothenburg. Sahlgrenska Academy
Institution
Institute of Neuroscience and Physiology. Department of Clinical Neuroscience and Rehabilitation
Disputation
Torsdagen den 4 juni 2009, kl. 13.00, Hörsal Ivan Östholm, Medicinaregatan 13, Göteborg
Date of defence
2009-06-04
E-mail
nina.hellstrom@neuro.gu.se
URI
http://hdl.handle.net/2077/19631
Collections
  • Doctoral Theses / Doktorsavhandlingar Institutionen för neurovetenskap och fysiologi
  • Doctoral Theses from Sahlgrenska Academy
  • Doctoral Theses from University of Gothenburg / Doktorsavhandlingar från Göteborgs universitet
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Thesis frame (695.7Kb)
Abstract (56.17Kb)
Cover (2.220Mb)
Date
2009-05-14
Author
Hellström, Nina
Keywords
ionizing radiation
neurogenesis
neural stem cells
inflammation
microglia
stem cell niche
trophic support
Publication type
Doctoral thesis
ISBN
978-91-628-7768-2
Language
eng
Metadata
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