Time-dependent neurosphere-forming ability of adult rat spinal cord after irradiation

被引:6
作者
Lu, Fred G. [1 ]
Wong, C. Shun [1 ]
机构
[1] Univ Toronto, Sunnybrook Hlth Sci Ctr, Dept Radiat Oncol, Discipline Cell & Mol Biol, Toronto, ON M4N 3M5, Canada
关键词
D O I
10.1667/RR0591.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To determine whether there was evidence for long-term time-dependent changes in neurosphere-forming ability of rat spinal cord after irradiation, a 15-mm length of spinal cord (C2-T2) of 10-week-old female rats was irradiated with a single dose of 2, 5, 10 or 19 Gy. Cells were isolated from the central 10-mm segment of the irradiated spinal cord immediately or at 0.5, 1, 2 or 5 months to form neurospheres. The number and sizes of neurospheres were determined at day 10, 12, 14 and 16 in vitro. The multipotential properties of neurosphere cells were assessed by immunocytochemistry using lineage-specific markers for neurons and glia. In nonirradiated controls, the number and size of the neurospheres decreased with increasing age of the animals. Regardless of the time after irradiation, there was a dose-dependent decrease in the number and size of neurospheres obtained from the irradiated cord compared to age-matched controls. Using threeway ANOVA, the number of neurospheres was dependent on radiation dose (P < 0.0001), time after irradiation (P < 0.0001), and day of counting in vitro (P < 0.0001). Compared to cells cultured immediately after irradiation, there was an increase in the relative plating efficiency of neurospheres cultured I month after irradiation. However, no further increase was apparent up to 5 months after irradiation. The multipotential properties of neurosphere cells in vitro remained unchanged with increasing time after irradiation. These results may suggest a time-dependent recovery of radiation damage using neurosphere-forming ability as the end point and agree with data that show time-dependent recovery of radiation damage in spinal cord using histological or functional end points. (C) 2007 by Radiation Research Society.
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页码:453 / 461
页数:9
相关论文
共 45 条
[1]   Extent and kinetics of recovery of occult spinal cord injury [J].
Ang, KK ;
Jiang, GL ;
Feng, Y ;
Stephens, LC ;
Tucker, SL ;
Price, RE .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 50 (04) :1013-1020
[2]   Apoptosis and proliferation of oligodendrocyte progenitor cells in the irradiated rodent spinal cord [J].
Atkinson, SL ;
Li, YQ ;
Wong, CS .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 62 (02) :535-544
[3]   Radiation induced CNS toxicity - molecular and cellular mechanisms [J].
Belka, C ;
Budach, W ;
Kortmann, R ;
Bamberg, M .
BRITISH JOURNAL OF CANCER, 2001, 85 (09) :1233-1239
[4]   Neural stem cells as therapeutic agents for age-related brain repair [J].
Bernal, GM ;
Peterson, DA .
AGING CELL, 2004, 3 (06) :345-351
[5]   Neurospheres: Insights biology into neural stem cell biology [J].
Campos, LS .
JOURNAL OF NEUROSCIENCE RESEARCH, 2004, 78 (06) :761-769
[6]   Oligodendrocyte progenitor cell (OPC) transplantation is unlikely to offer a means of preventing X-irradiation induced damage in the CNS [J].
Chari, DM ;
Gilson, JM ;
Franklin, RJM ;
Blakemore, WF .
EXPERIMENTAL NEUROLOGY, 2006, 198 (01) :145-153
[7]   Radiation-induced apoptosis in the adult central nervous system is p53-dependent [J].
Chow, BM ;
Li, YQ ;
Wong, CS .
CELL DEATH AND DIFFERENTIATION, 2000, 7 (08) :712-720
[8]   Neurogenesis and brain injury: managing a renewable resource for repair [J].
Hallbergson, AF ;
Gnatenco, C ;
Peterson, DA .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (08) :1128-1133
[9]   Directed migration of neural stem cells to sites of CNS injury by the stromal cell-derived factor 1α/CXC chemokine receptor 4 pathway [J].
Imitola, J ;
Raddassi, K ;
Park, KI ;
Mueller, FJ ;
Nieto, M ;
Teng, YD ;
Frenkel, D ;
Li, JX ;
Sidman, RL ;
Walsh, CA ;
Snyder, EY ;
Khoury, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (52) :18117-18122
[10]   Transplanted human fetal neural stem cells survive, migrate, and differentiate in ischemic rat cerebral cortex [J].
Kelly, S ;
Bliss, TM ;
Shah, AK ;
Sun, GH ;
Ma, M ;
Foo, WC ;
Masel, J ;
Yenari, MA ;
Weissman, IL ;
Uchida, N ;
Palmer, T ;
Steinberg, GK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (32) :11839-11844