Temporal variability of jun family transcription factor levels in peripherally or centrally transected adult rat dorsal root ganglia

被引:22
作者
Kenney, AM
Kocsis, JD
机构
[1] YALE UNIV,VET ADM MED CTR,SCH MED,NEUROSCI RES CTR 127A,W HAVEN,CT 06516
[2] YALE UNIV,SCH MED,DEPT NEUROL,W HAVEN,CT 06510
来源
MOLECULAR BRAIN RESEARCH | 1997年 / 52卷 / 01期
关键词
axotomy; brain-derived neurotrophic factor; c-jun; dorsal root ganglion; JunB; JunD; nerve growth factor; rhizotomy;
D O I
10.1016/S0169-328X(97)00211-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Enhanced chemiluminescent (ECL) immunoblotting was used to quantitatively assess the initial changes in jun family transcription factor protein levels in adult rat lumbar dorsal root ganglia (DRG) after peripheral axotomy and dorsal root transection, and to study the effects of neurotrophic factor administration on these changes. Transection of central (dorsal root) or peripheral (spinal nerve) branches of DRG neurons resulted in rapid elevation of c-jun protein levels, which was transient after dorsal root transection but sustained, though slightly attenuated, after spinal nerve transection. These results suggest that injury-induced c-jun elevation is biphasic, consisting of an early, transient, injury-initiated phase and a more prolonged secondary phase specific to peripheral target disconnection. c-jun protein changes were not modulated by administration of NGF or BDNF. Immunohistochemistry was used to localize c-jun protein induction to DRG neurons. Using ECL immunoblotting, we also observed temporally regulated increases in junD protein levels after both injuries. A transient up-regulation of junB was detected by immunoblotting 5 days after peripheral axotomy, coincident with a slight decrease in c-jun protein levels. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:53 / 61
页数:9
相关论文
共 62 条
[1]   THE JUN PROTO-ONCOGENE IS POSITIVELY AUTOREGULATED BY ITS PRODUCT, JUN/AP-1 [J].
ANGEL, P ;
HATTORI, K ;
SMEAL, T ;
KARIN, M .
CELL, 1988, 55 (05) :875-885
[2]   CELL LOSS IN LUMBAR DORSAL-ROOT GANGLIA AND TRANSGANGLIONIC DEGENERATION AFTER SCIATIC-NERVE RESECTION IN THE RAT [J].
ARVIDSSON, J ;
YGGE, J ;
GRANT, G .
BRAIN RESEARCH, 1986, 373 (1-2) :15-21
[3]   DIFFERENTIAL MACROPHAGE RESPONSES IN THE PERIPHERAL AND CENTRAL-NERVOUS-SYSTEM DURING WALLERIAN DEGENERATION OF AXONS [J].
AVELLINO, AM ;
HART, D ;
DAILEY, AT ;
MACKINNON, M ;
ELLEGALA, D ;
KLIOT, M .
EXPERIMENTAL NEUROLOGY, 1995, 136 (02) :183-198
[4]   REVERSAL OF AXONAL-TRANSPORT AT A NERVE CRUSH [J].
BISBY, MA ;
BULGER, VT .
JOURNAL OF NEUROCHEMISTRY, 1977, 29 (02) :313-320
[5]   JUN-B DIFFERS IN ITS BIOLOGICAL PROPERTIES FROM, AND IS A NEGATIVE REGULATOR OF, C-JUN [J].
CHIU, R ;
ANGEL, P ;
KARIN, M .
CELL, 1989, 59 (06) :979-986
[6]  
Chong MS, 1996, J COMP NEUROL, V370, P97, DOI 10.1002/(SICI)1096-9861(19960617)370:1<97::AID-CNE9>3.0.CO
[7]  
2-G
[8]   WHAT IS SIGNAL FOR CHROMATOLYSIS [J].
CRAGG, BG .
BRAIN RESEARCH, 1970, 23 (01) :1-+
[9]   COMPARISON OF C-JUN, JUNB, AND JUND MESSENGER-RNA EXPRESSION AND PROTEIN IN THE RAT DORSAL-ROOT GANGLIA FOLLOWING SCIATIC-NERVE TRANSECTION [J].
DELEON, M ;
NAHIN, RL ;
MOLINA, CA ;
DELEON, DD ;
RUDA, MA .
JOURNAL OF NEUROSCIENCE RESEARCH, 1995, 42 (03) :391-401
[10]   JUNB DIFFERS FROM C-JUN IN ITS DNA-BINDING AND DIMERIZATION DOMAINS, AND REPRESSES C-JUN BY FORMATION OF INACTIVE HETERODIMERS [J].
DENG, TL ;
KARIN, M .
GENES & DEVELOPMENT, 1993, 7 (03) :479-490