Feng Z, Zhang W, Hudson P, Bing G, Feng W, Hong J S
Neuropharmacology Section, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709, USA.
Brain Res. 1997 Oct 3;770(1-2):53-9. doi: 10.1016/s0006-8993(97)00744-0.
Kainic acid is known to induce seizures, neuronal damage and cell loss in the rat hippocampus. Our laboratory has shown that a single kainic acid injection elicits acute increases of activator protein-1 DNA-binding activity and this activity stays at an elevated level for 2 weeks after kainic acid injection. However, some pathological changes such as mossy fiber sprouting do not occur until 2-3 weeks after the kainic acid injection and the specific transcription factors regulating the long-term events after kainic acid treatment are not clear. To determine the involvement of activator protein-1 transcription factors in the long-term events after kainic acid treatment, gel mobility-shift and Western blot analyses were used. The results showed that two activator protein-1 complexes with different mobilities occur during the acute stage. However, only the faster-migrating complex as well as the 35-37-kDa fos-related antigen and Jun-D proteins were seen during the late stage. These results suggest that different activator protein-1 complexes exist at different stages after convulsions and that they regulate ensembles of different genes.
已知海藻酸可诱导大鼠海马体发生癫痫、神经元损伤和细胞丢失。我们实验室已表明,单次注射海藻酸会引发激活蛋白-1 DNA结合活性的急性增加,且该活性在注射海藻酸后2周内一直维持在升高水平。然而,一些病理变化,如苔藓纤维发芽,直到注射海藻酸后2至3周才会出现,并且调节海藻酸处理后长期事件的特定转录因子尚不清楚。为了确定激活蛋白-1转录因子在海藻酸处理后的长期事件中的作用,我们进行了凝胶迁移率变动分析和蛋白质免疫印迹分析。结果表明,在急性期出现了两种迁移率不同的激活蛋白-1复合物。然而,在后期仅观察到迁移速度较快的复合物以及35 - 37 kDa的Fos相关抗原和Jun-D蛋白。这些结果表明,惊厥后不同阶段存在不同的激活蛋白-1复合物,并且它们调节不同的基因组合。