Akiyama Masahiro, Kanaho Yasunori
a Faculty of Medicine and Graduate School of Comprehensive Human Sciences; Department of Physiological Chemistry ; University of Tsukuba ; Tennodai, Tsukuba , Japan.
Small GTPases. 2015;6(3):160-4. doi: 10.1080/21541248.2015.1043041. Epub 2015 Aug 20.
The small GTPase ADP-ribosylation factor 6 (Arf6) plays important roles in membrane dynamics-based neuronal cell events such as neurite outgrowth and spine formation. However, physiological functions of Arf6 in the nervous system at whole animal level have not yet been explored. We have recently generated conditional knockout mice lacking Arf6 in neurons or oligodendrocytes of central nervous system (CNS) or both cell lineages, and analyzed them. We found that ablation of Arf6 gene from neurons, but not from oligodendrocytes, caused the defect in axon myelination at the fimbria of hippocampus (Fim) and corpus callosum (CC). We also found that migration of oligodendrocyte precursor cells (OPCs) from the subventricular zone to the Fim and CC in mice lacking Arf6 in neurons was impaired. Finally, it was found that secretion of fibroblast growth factor-2 (FGF-2), a guidance factor for OPC migration, from hippocampi lacking Arf6 was impaired. Collectively, these findings demonstrate that Arf6 in neurons of the CNS plays an important role in OPC migration by regulating secretion of FGF-2 from neurons, thereby contributing to the axon myelination. Here, we discuss our current understanding of physiological functions of Arf6 in the nervous system.
小GTP酶ADP核糖基化因子6(Arf6)在基于膜动力学的神经元细胞事件中发挥重要作用,如神经突生长和树突棘形成。然而,Arf6在整个动物水平的神经系统中的生理功能尚未得到探索。我们最近生成了在中枢神经系统(CNS)的神经元或少突胶质细胞或这两种细胞谱系中缺乏Arf6的条件性敲除小鼠,并对其进行了分析。我们发现,从神经元而非少突胶质细胞中敲除Arf6基因会导致海马伞(Fim)和胼胝体(CC)的轴突髓鞘形成缺陷。我们还发现,在神经元中缺乏Arf6的小鼠中,少突胶质细胞前体细胞(OPC)从脑室下区向Fim和CC的迁移受损。最后,发现缺乏Arf6的海马体中成纤维细胞生长因子2(FGF-2,一种OPC迁移的导向因子)的分泌受损。总的来说,这些发现表明,中枢神经系统神经元中的Arf6通过调节神经元中FGF-2的分泌在OPC迁移中起重要作用,从而有助于轴突髓鞘形成。在此,我们讨论目前对Arf6在神经系统中生理功能的理解。