Shimomura Atsushi, Kohu Kazuyoshi, Akiyama Tetsu, Senda Takao
Department of Anatomy I, School of Medicine, Fujita Health University, 1-98, Toyoake, Aichi 470-1192, Japan.
Neurosci Lett. 2005 Feb 28;375(2):81-6. doi: 10.1016/j.neulet.2004.10.074. Epub 2004 Dec 10.
We examined the subcellular distribution of tumor suppressor adenomatous polyposis coli (APC) in developing cultured rat hippocampal neurons using both immunofluorescent microscopy and immunoelectron microscopy. APC initially localized at the distal tips of all the cell processes. Between 12 and 24 h after plating, APC concentrated at the growth cone and in the distal portion of the longest process, which was growing very rapidly. The other processes, growing at a much slower rate, showed only weak immunoreactivity for APC. After maturation of the neurons, APC in the axons was restricted to the growth cones and distal portions. In contrast, APC formed a punctuated pattern along the dendritic processes. This subcellular distribution of APC was dependent on the organization of microtubules, but not actin filaments. Moreover, treatment of neurons with a PKCzeta specific inhibitor caused defects in the staining pattern of APC. These results suggest that APC may be involved in neuronal process extension, and that APC may exert different functions on axons and dendritic processes.
我们使用免疫荧光显微镜和免疫电子显微镜,研究了肿瘤抑制因子腺瘤性息肉病大肠杆菌(APC)在培养的发育中大鼠海马神经元中的亚细胞分布。APC最初定位于所有细胞突起的远端。接种后12至24小时之间,APC集中在生长锥和生长非常迅速的最长突起的远端部分。其他生长速度慢得多的突起,对APC仅显示出微弱的免疫反应性。神经元成熟后,轴突中的APC局限于生长锥和远端部分。相反,APC沿树突状突起形成点状模式。APC的这种亚细胞分布取决于微管的组织,而不是肌动蛋白丝。此外,用PKCzeta特异性抑制剂处理神经元会导致APC染色模式出现缺陷。这些结果表明,APC可能参与神经元突起的延伸,并且APC可能在轴突和树突状突起上发挥不同的功能。