Takamori Nobutake, Shimomura Atsushi, Senda Takao
Department of Anatomy I, School of Medicine, Fujita Health University, Toyoake, Aichi 470-1192, Japan.
Neurosci Lett. 2006 Jul 31;403(1-2):68-72. doi: 10.1016/j.neulet.2006.04.045. Epub 2006 May 15.
Adenomatous polyposis coli (APC) tumor suppressor protein binds to microtubules, leading to microtubule bundling and stabilization. The protein also interacts with postsynaptic density (PSD)-95, a major scaffolding protein in neurons. Here, we analyzed the effects of PSD-95 on the microtubule-bundling activity of APC. The coexpression of APC and PSD-95 in COS-7 cells enhanced microtubule-bundle formation compared with the expression of APC alone. A mutant APC variant that does not associate with PSD-95 did not enhance microtubule bundling, despite coexpression with PSD-95. Immunoelectron microscopy showed that the APC-PSD-95 complex sometimes colocalized on microtubules in processes of cultured neurons. These results suggest that the microtubule-bundling activity of APC is regulated by its interaction with PSD-95, which might modulate microtubule architecture and dynamics in neurons.
腺瘤性结肠息肉病蛋白(APC)肿瘤抑制蛋白与微管结合,导致微管成束并稳定。该蛋白还与神经元中主要的支架蛋白突触后致密蛋白(PSD)-95相互作用。在此,我们分析了PSD-95对APC微管成束活性的影响。与单独表达APC相比,在COS-7细胞中共表达APC和PSD-95增强了微管束的形成。尽管与PSD-95共表达,但不与PSD-95结合的突变型APC变体并未增强微管成束。免疫电子显微镜显示,APC-PSD-95复合物有时在培养神经元的突起中的微管上共定位。这些结果表明,APC的微管成束活性受其与PSD-95相互作用的调节,这可能会调节神经元中的微管结构和动力学。