Kenney A M, Kocsis J D
Department of Neurology, Yale University School of Medicine, New Haven, CT 06510, USA.
Brain Res Mol Brain Res. 1997 Dec 1;52(1):53-61. doi: 10.1016/s0169-328x(97)00211-8.
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.
增强化学发光(ECL)免疫印迹法用于定量评估成年大鼠腰段背根神经节(DRG)在周围神经切断术和背根切断术后Jun家族转录因子蛋白水平的初始变化,并研究神经营养因子给药对这些变化的影响。DRG神经元的中枢(背根)或外周(脊神经)分支切断导致c-Jun蛋白水平迅速升高,背根切断后这种升高是短暂的,但脊神经切断后持续存在,尽管略有减弱。这些结果表明,损伤诱导的c-Jun升高是双相的,包括早期短暂的损伤起始阶段和外周靶标断开特有的更持久的第二阶段。c-Jun蛋白变化不受NGF或BDNF给药的调节。免疫组织化学用于将c-Jun蛋白诱导定位到DRG神经元。使用ECL免疫印迹法,我们还观察到两种损伤后JunD蛋白水平的时间性调节增加。在外周神经切断术后5天通过免疫印迹检测到JunB的短暂上调,与c-Jun蛋白水平略有下降一致。