Regionally and temporally distinct patterns of induction of c-fos, c-jun and junB mRNAs following experimental brain injury in the rat

被引:67
作者
Raghupathi, R
McIntosh, TK
机构
[1] Division of Neurosurgery, Department of Surgery, Univ. of Pennyslvania Sch. of Med., Philadelphia, PA
来源
MOLECULAR BRAIN RESEARCH | 1996年 / 37卷 / 1-2期
关键词
immediate early genes; c-fos; c-jun; JunB; traumatic brain injury;
D O I
10.1016/0169-328X(95)00289-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Lateral (parasagittal) fluid-percussion brain injury of mild (1.0-1.5 atm) and moderate (2.1-2.4 atm) severity induced expression of mRNAs for the immediate early genes (IEGs) c-fos, c-jun and junB. At 5 min following mild brain injury, c-fos and junB mRNA were co-induced in the cortex ipsilateral to the impact site. Expression remained elevated up to 2 h after injury and returned to control levels by 6 h. Levels of c-fos mRNA increased in the cells of the hippocampal dentate gyrus as early as 5 min after mild brain injury and additionally in the areas CA(1-3) by 30 min. By 2 h, no hippocampal c-fos mRNA was detectable. Induction of junB mRNA in the hippocampus was delayed, occurring at 30 min after injury, and remained elevated up to 2 h post injury. Increased levels of junB mRNA were also observed in the striatum ipsilateral to the injury. Increased expression of c-jun mRNA was restricted to the ipsilateral dentate gyrus and was observed at 5 min after injury and remained elevated up to 6 h. Although the temporal pattern of induction of individual IEGs after brain injury of moderate severity was similar to that observed after mild severity, moderate injury induced IEG mRNA in both injured and contralateral hemispheres. These data suggest that traumatic brain injury invokes a complex acute regional and cellular response which may involve the activation of multiple signal transduction pathways.
引用
收藏
页码:134 / 144
页数:11
相关论文
共 46 条
[1]   EXPRESSION OF C-FOS AND C-JUN FAMILY GENES AFTER FOCAL CEREBRAL-ISCHEMIA [J].
AN, G ;
LIN, TN ;
LIU, JS ;
XUE, JJ ;
HE, YY ;
HSU, CY .
ANNALS OF NEUROLOGY, 1993, 33 (05) :457-464
[2]  
ARENANDER A, 1992, PROG BRAIN RES, V94, P177
[3]   REGULATION OF GENE-EXPRESSION IN HIPPOCAMPAL-NEURONS BY DISTINCT CALCIUM SIGNALING PATHWAYS [J].
BADING, H ;
GINTY, DD ;
GREENBERG, ME .
SCIENCE, 1993, 260 (5105) :181-186
[4]   GROWTH-FACTORS AND MEMBRANE DEPOLARIZATION ACTIVATE DISTINCT PROGRAMS OF EARLY RESPONSE GENE-EXPRESSION - DISSOCIATION OF FOS AND JUN INDUCTION [J].
BARTEL, DP ;
SHENG, M ;
LAU, LF ;
GREENBERG, ME .
GENES & DEVELOPMENT, 1989, 3 (03) :304-313
[5]  
CURRAN T, 1987, ONCOGENE, V2, P79
[6]   STRUCTURAL AND FUNCTIONAL IDENTIFICATION OF REGULATORY REGIONS AND CIS ELEMENTS SURROUNDING THE NERVE GROWTH-FACTOR GENE PROMOTER [J].
D'MELLO, SR ;
HEINRICH, G .
MOLECULAR BRAIN RESEARCH, 1991, 11 (3-4) :255-264
[7]   UP-REGULATION OF NERVE GROWTH-FACTOR FOLLOWING CORTICAL TRAUMA [J].
DEKOSKY, ST ;
GOSS, JR ;
MILLER, PD ;
STYREN, SD ;
KOCHANEK, PM ;
MARION, D .
EXPERIMENTAL NEUROLOGY, 1994, 130 (02) :173-177
[8]   MK-801, AN ANTAGONIST OF NMDA RECEPTORS, INHIBITS INJURY-INDUCED C-FOS PROTEIN ACCUMULATION IN RAT-BRAIN [J].
DRAGUNOW, M ;
FAULL, RLM ;
JANSEN, KLR .
NEUROSCIENCE LETTERS, 1990, 109 (1-2) :128-133
[9]   BRAIN INJURY INDUCES C-FOS PROTEIN(S) IN NERVE AND GLIAL-LIKE CELLS IN ADULT MAMMALIAN BRAIN [J].
DRAGUNOW, M ;
ROBERTSON, HA .
BRAIN RESEARCH, 1988, 455 (02) :295-299
[10]   IS C-JUN INVOLVED IN NERVE-CELL DEATH FOLLOWING STATUS EPILEPTICUS AND HYPOXIC-ISCHEMIC BRAIN INJURY [J].
DRAGUNOW, M ;
YOUNG, D ;
HUGHES, P ;
MACGIBBON, G ;
LAWLOR, P ;
SINGLETON, K ;
SIRIMANNE, E ;
BEILHARZ, E ;
GLUCKMAN, P .
MOLECULAR BRAIN RESEARCH, 1993, 18 (04) :347-352