Morita Hiroyuki, Suzuki Katsuaki, Mori Norio, Yasuhara Osamu
Molecular Neuroscience Research Center, Shiga University of Medical Science, Seta Tsukinowa-cho, Otsu, Shiga 520-2192, Japan.
Neurosci Lett. 2006 Nov 27;409(1):35-40. doi: 10.1016/j.neulet.2006.09.037. Epub 2006 Oct 2.
To evaluate the roles of complement in kainic acid (KA)-induced neuronal damages, the immunohistochemical localization of the complement protein C3 was examined in rat hippocampus after systemic KA injection. The immunoreactivity for C3 was found in glial cells in control rats, and such glial cells were increased in number after KA injection. Our confocal study showed that C3-positive glial cells were microglia. Three to seven days after KA, C3 immunoreactivity appeared in CA1 and CA3 pyramidal neurons. Double staining for C3 combined with the terminal deoxynucleotidyl transferase-mediated dUTP nick end labelling showed that occurrence of C3 immunoreactivity in neurons coincided well with that of DNA fragmentation. Western blot analysis and RT-PCR experiments suggested local synthesis of C3 by brain cells. Our results suggest that C3 contributes greatly to neuronal death after systemic KA administration, and that microglia and neurons are the local source of C3 in KA-induced brain injury.
为了评估补体在 kainic 酸(KA)诱导的神经元损伤中的作用,在全身注射 KA 后,检测大鼠海马中补体蛋白 C3 的免疫组化定位。在对照大鼠的胶质细胞中发现了 C3 的免疫反应性,KA 注射后此类胶质细胞数量增加。我们的共聚焦研究表明,C3 阳性胶质细胞是小胶质细胞。KA 注射后 3 至 7 天,CA1 和 CA3 锥体神经元中出现 C3 免疫反应性。C3 与末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记的双重染色表明,神经元中 C3 免疫反应性的出现与 DNA 片段化的出现非常吻合。蛋白质印迹分析和逆转录-聚合酶链反应实验表明脑细胞可局部合成 C3。我们的结果表明,C3 在全身注射 KA 后对神经元死亡有很大贡献,并且小胶质细胞和神经元是 KA 诱导的脑损伤中 C3 的局部来源。