Induction of c-fos and junB mRNA following in vivo brain irradiation

被引:22
作者
Hong, JH
Chiang, CS
Sun, JR
Withers, HR
McBride, WH
机构
[1] TSING HUA UNIV,DEPT NUCL SCI,HSING TZU,TAIWAN
[2] UNIV CALIF LOS ANGELES,SCH MED,DEPT RADIAT ONCOL,LOS ANGELES,CA
来源
MOLECULAR BRAIN RESEARCH | 1997年 / 48卷 / 02期
关键词
brain irradiation; gene expression; c-fos; junB; pentobarbital; glucocorticoid; IMMEDIATE-EARLY GENES; PROTEIN-LIKE IMMUNOREACTIVITY; RADIATION-INDUCED APOPTOSIS; NERVE GROWTH-FACTOR; RAT SPINAL-CORD; IONIZING-RADIATION; EARLY RESPONSE; MESSENGER-RNA; GAMMA-RAYS; HEAT-SHOCK;
D O I
10.1016/S0169-328X(97)00095-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although radiotherapy is a front line treatment for brain tumors, little is known about the in vivo molecular responses of brain to irradiation. In this study, expression of c-fos, c-jun and junB immediate-early genes were followed in mouse brain after irradiation. C-fos and junB, but not c-jun, mRNA was induced within 15 min in unanesthetized irradiated mice. Induction was transient and lasted < 4 h. The response was dose-dependent with increases in c-Sos and junB mRNA levels after dose of greater than or equal to 2 and 7 Gy, respectively. Anesthesia of mice with pentobarbitol delayed the increases in mRNA expression and the response was attenuated. Pre-treatment of mice with dexamethasone, in a schedule which suppressed acute-phase gene expression after brain irradiation, did not significantly change c-fas and junB induction. Our results show that c-fos and junB responses occur in the brain in response to irradiation and that they can be modified by pentobarbital treatment but suggest that there is no direct correlation between the level of mRNA expression and later expression of cytokines or other acute-phase response genes.
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页码:223 / 228
页数:6
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