Pennypacker K R, Lennard D E, Hudson P M, Hong J S, McMillian M K
Laboratory of Environmental Neuroscience, National Institute of Environmental Health Sciences, NC 27709, USA.
Brain Res Mol Brain Res. 1995 Dec 1;34(1):161-5. doi: 10.1016/0169-328x(95)00164-n.
Recently, there have been a number of reports showing a long-term increased expression of fos-related antigens (fra), molecular weight of 35 kDa, after brain injury or chronic treatment of rats with various drugs. We report elevated basal levels of this transcription factor in the olfactory bulb relative to other brain regions. The expression of this protein is further enhanced in the olfactory bulb as long as 3 months after a single injection of kainate, an effect similar to that we previously observed in the hippocampus. The AP-1 DNA binding activity in olfactory bulb from kainate-treated rats contains fra and jun immunoreactivity suggesting that the 35 kDa fra dimerizes with jun protein, probably junD, to bind to AP-1 sites. Elevated basal levels of this transcription factor in the olfactory bulb appear to be related to the constant reinnervation and synaptogenesis which occurs in this brain region. The 35 kDa fra may be involved in long-term genomic program changes required to adapt to an altered biochemical environment.
最近,有许多报道显示,在脑损伤或用各种药物对大鼠进行长期治疗后,分子量为35 kDa的Fos相关抗原(fra)的表达会长期增加。我们报告称,相对于其他脑区,嗅球中这种转录因子的基础水平有所升高。单次注射红藻氨酸后长达3个月,该蛋白在嗅球中的表达会进一步增强,这一效应与我们之前在海马体中观察到的相似。经红藻氨酸处理的大鼠嗅球中的AP-1 DNA结合活性含有fra和jun免疫反应性,这表明35 kDa的fra与jun蛋白(可能是junD)二聚化,以结合到AP-1位点。嗅球中这种转录因子基础水平的升高似乎与该脑区持续的神经再支配和突触形成有关。35 kDa的fra可能参与了适应改变的生化环境所需的长期基因组程序变化。