Ikuta Junko, Maturana Andrés, Fujita Toshitsugu, Okajima Toshihide, Tatematsu Kenji, Tanizawa Katsuyuki, Kuroda Shun'ichi
Department of Structural Molecular Biology, Institute of Scientific and Industrial Research, Osaka University, Ibaraki, Osaka 567-0047, Japan.
Biochem Biophys Res Commun. 2007 Feb 2;353(1):127-32. doi: 10.1016/j.bbrc.2006.11.142. Epub 2006 Dec 6.
The fasciculation and elongation protein zeta-1 (FEZ1), a mammalian orthologue of Caenorhabditis elegans UNC-76 protein, is a 45-kDa protein with four coiled-coiled domains and efficiently promotes the neurite elongation in the rat phaeochromocytoma PC12 cells. UNC-76 proteins of C. elegans and Drosophila have been genetically demonstrated to be involved in the axonal guidance. We here show that FEZ1 RNA interference (RNAi) represses the formation of axon in rat embryo hippocampal neurons. An anterograde mitochondrial movement is also retarded in neurites of the RNAi-treated hippocampal neurons. Moreover, the size of mitochondria is considerably elongated by the RNAi treatment. The transport of mitochondria from soma to axon or dendrites is essential for the neuronal differentiation. Therefore, our results strongly suggest that FEZ1 participates in the establishment of neuronal polarity by controlling the mitochondrial motility along axon.
成束和延伸蛋白ζ-1(FEZ1)是秀丽隐杆线虫UNC-76蛋白的哺乳动物同源物,是一种具有四个卷曲螺旋结构域的45 kDa蛋白,可有效促进大鼠嗜铬细胞瘤PC12细胞中的神经突延伸。秀丽隐杆线虫和果蝇的UNC-76蛋白已通过遗传学证明参与轴突导向。我们在此表明,FEZ1 RNA干扰(RNAi)可抑制大鼠胚胎海马神经元中轴突的形成。在经RNAi处理的海马神经元的神经突中,顺向线粒体运动也受到阻碍。此外,RNAi处理可使线粒体的大小显著延长。线粒体从胞体向轴突或树突的运输对于神经元分化至关重要。因此,我们的结果强烈表明,FEZ1通过控制沿轴突的线粒体运动性参与神经元极性的建立。