High-LET radiation induces inflammation and persistent changes in markers of hippocampal neurogenesis

被引:110
作者
Rola, R
Sarkissian, V
Obenaus, A
Nelson, GA
Otsuka, S
Limoli, CL
Fike, JR
机构
[1] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Radiat Oncol, San Francisco, CA 94143 USA
[3] Loma Linda Univ, Radiobiol Program, Loma Linda, CA 92354 USA
[4] Univ Lublin, Sch Med, Dept Neurol Surg, PL-20950 Lublin, Poland
关键词
D O I
10.1667/RR3412.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Exposure to heavy-ion radiation is considered a potential health risk in long-term space travel. It may result in the loss of critical cellular components in complex systems like the central nervous system (CNS), which could lead to performance decrements that ultimately could compromise mission goals and long-term quality of life. Specific hippocampal-dependent cognitive impairment occurs after whole-body Fe-56-particle irradiation, and while the pathogenesis of this effect is not yet clear, it may involve damage to neural precursor cells in the hippocampal dentate gyrus. We irradiated mice with 1-3 Gy of C-12 or Fe-56 ions and 9 months later quantified proliferating cells and immature neurons in the dentate subgranular zone (SGZ). Our results showed that reductions in these cells were dependent on the dose and LET. When compared with data for mice that were studied 3 months after 56Fe-particle irradiation, our current data suggest that these changes are not only persistent but may worsen with time. Loss of precursor cells was also associated with altered neurogenesis and a robust inflammatory response. These results indicate that high-LET radiation has a significant and long-lasting effect on the neurogenic population in the hippocampus that involves cell loss and changes in the microenvironment. (c) 2005 by Radiation Research Society.
引用
收藏
页码:556 / 560
页数:5
相关论文
共 25 条
[1]   Distribution, cellular localization and functional role of CCR2 chemokine receptors in adult rat brain [J].
Banisadr, G ;
Quéraud-Lesaux, F ;
Boutterin, MC ;
Pélaprat, D ;
Zalc, B ;
Rostène, W ;
Haour, F ;
Parsadaniantz, SM .
JOURNAL OF NEUROCHEMISTRY, 2002, 81 (02) :257-269
[2]  
Curtis S B, 1989, Adv Space Res, V9, P293, DOI 10.1016/0273-1177(89)90452-3
[3]   Chemokines and disease [J].
Gerard, C ;
Rollins, BJ .
NATURE IMMUNOLOGY, 2001, 2 (02) :108-115
[4]  
Higuchi Y, 2002, J RADIAT RES, V43, pS219
[5]  
Kuhn HG, 1996, J NEUROSCI, V16, P2027
[6]   Arrested neuronal proliferation and impaired hippocampal function following fractionated brain irradiation in the adult rat [J].
Madsen, TM ;
Kristjansen, PEG ;
Bolwig, TG ;
Wörtwein, G .
NEUROSCIENCE, 2003, 119 (03) :635-642
[7]  
Mizumatsu S, 2003, CANCER RES, V63, P4021
[8]   Inflammatory blockade restores adult hippocampal neurogenesis [J].
Monje, ML ;
Toda, H ;
Palmer, TD .
SCIENCE, 2003, 302 (5651) :1760-1765
[9]   Irradiation induces neural precursor-cell dysfunction [J].
Monje, ML ;
Mizumatsu, S ;
Fike, JR ;
Palmer, TD .
NATURE MEDICINE, 2002, 8 (09) :955-962
[10]   Selective vulnerability to radiation in the hippocampal dentate granule cells [J].
Nagai, R ;
Tsunoda, S ;
Hori, Y ;
Asada, H .
SURGICAL NEUROLOGY, 2000, 53 (05) :503-506