DIFFERENTIAL EXPRESSION OF IMMEDIATE EARLY GENES IN THE HIPPOCAMPUS IN THE KINDLING MODEL OF EPILEPSY

被引:104
作者
SIMONATO, M
HOSFORD, DA
LABINER, DM
SHIN, C
MANSBACH, HH
MCNAMARA, JO
机构
[1] VET ADM MED CTR,BLDG 16,RM 20,508 FULTON ST,DURHAM,NC 27705
[2] DUKE UNIV,DIV NEUROL,DUKE CTR ADV STUDY EPILEPSY,DURHAM,NC 27706
来源
MOLECULAR BRAIN RESEARCH | 1991年 / 11卷 / 02期
基金
美国国家卫生研究院;
关键词
IMMEDIATE EARLY GENE; KINDLING; C-FOS; HIPPOCAMPUS; C-JUN; C-MYC; DENTATE GYRUS; NGFI-A; INSITU HYBRIDIZATION HISTOCHEMISTRY;
D O I
10.1016/0169-328X(91)90113-C
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Kindling is a phenomenon in which brief afterdischarges (ADs) evoked by periodic electrical stimulation of the brain eventually result in generalized clonic motor seizures. Once present, the enhanced sensitivity to electrical stimulation is lifelong. The mechanism by which brief ADs produce this long-lasting effect may involve a change in gene expression. To begin to investigate changes in gene expression that occur during kindling, we used in situ hybridization histochemistry to examine the time course of expression of mRNAs of the immediate early genes (IEGs) c-fos, c-jun, NGFI-A, and c-myc within the dorsal hippocampus of rats following a kindling AD. Three principal findings resulted from this study. First, the expression of all mRNAs except c-myc was significantly increased (P < 0.05) within discrete neuronal populations. Second, the time course of expression of the IEGs differed markedly within the same neuronal population. Third, for a given IEG, the time course and anatomic pattern of expression were strikingly different among different neuronal populations of the hippocampus. The prolonged and distinctly different patterns of IEG expression suggest that target genes are differentially regulated in these neuronal populations for prolonged periods following a kindling AD.
引用
收藏
页码:115 / 124
页数:10
相关论文
共 50 条
[1]   COMPLEXITY OF THE EARLY GENETIC RESPONSE TO GROWTH-FACTORS IN MOUSE FIBROBLASTS [J].
ALMENDRAL, JM ;
SOMMER, D ;
MACDONALDBRAVO, H ;
BURCKHARDT, J ;
PERERA, J ;
BRAVO, R .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2140-2148
[2]   ONCOGENE JUN ENCODES A SEQUENCE-SPECIFIC TRANS-ACTIVATOR SIMILAR TO AP-1 [J].
ANGEL, P ;
ALLEGRETTO, EA ;
OKINO, ST ;
HATTORI, K ;
BOYLE, WJ ;
HUNTER, T ;
KARIN, M .
NATURE, 1988, 332 (6160) :166-171
[3]   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
[4]   DNA-BINDING SITE OF THE GROWTH FACTOR-INDUCIBLE PROTEIN ZIF268 [J].
CHRISTY, B ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8737-8741
[5]   A GENE ACTIVATED IN MOUSE 3T3-CELLS BY SERUM GROWTH-FACTORS ENCODES A PROTEIN WITH ZINC FINGER SEQUENCES [J].
CHRISTY, BA ;
LAU, LF ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) :7857-7861
[6]   FRA-1 - A SERUM-INDUCIBLE, CELLULAR IMMEDIATE-EARLY GENE THAT ENCODES A FOS-RELATED ANTIGEN [J].
COHEN, DR ;
CURRAN, T .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2063-2069
[7]   FOS AND JUN - THE AP-1 CONNECTION [J].
CURRAN, T ;
FRANZA, BR .
CELL, 1988, 55 (03) :395-397
[8]  
CURRAN T, 1984, CELL, V36, P259
[9]  
CURRAN T, 1987, ONCOGENE, V2, P74
[10]   AMYGDALA KINDLING AND C-FOS PROTEIN(S) [J].
DRAGUNOW, M ;
ROBERTSON, HA ;
ROBERTSON, GS .
EXPERIMENTAL NEUROLOGY, 1988, 102 (02) :261-263