Watanabe Yuji, Toyoda Reiko, Nakamura Harukazu
Department of Molecular Neurobiology, Institute of Development, Aging and Cancer, Tohoku University, Aoba-ku, Sendai 980-8575, Japan.
Development. 2004 Feb;131(3):681-92. doi: 10.1242/dev.00970.
Trochlear motor axons project dorsally along the midbrain-hindbrain boundary (MHB) to decussate at the dorsal midline. We report on the roles of neuropilin 2 and its ligands in the molecular mechanisms controlling this trajectory. In chick embryos, neuropilin 2 was expressed in the neuroepithelium of the dorsal isthmus in addition to the trochlear neurons, and Sema3F transcripts were localized along the caudal margin of the midbrain. Misexpression of Sema3F demonstrated that Sema3F displays repulsive activity in vivo that guides the trochlear motor axons along the MHB. An unexpected result was that misexpression of neuropilin 2 canceled the midbrain-evoked repulsion, allowing trochlear motor axons to cross the MHB and invade the tectum. A binding assay with neuropilin 2 ectodomain revealed the existence of neuropilin 2 ligands in the midbrain, which were masked by ectopic neuropilin 2. We therefore propose that neuropilin 2 neutralizes the repulsive activity in order to steer trochlear motor axons towards the dorsal decussation point. Taken together, our results suggest that the interaction of neuropilin 2 with its ligands has crucial roles for establishing trochlear trajectory along the MHB.
滑车神经运动轴突沿中脑-后脑边界(MHB)向背侧投射,在背侧中线处交叉。我们报告了神经纤毛蛋白2及其配体在控制这一轨迹的分子机制中的作用。在鸡胚中,神经纤毛蛋白2除了在滑车神经元中表达外,还在背侧峡部的神经上皮中表达,并且Sema3F转录本定位于中脑的尾缘。Sema3F的错误表达表明Sema3F在体内表现出排斥活性,可引导滑车神经运动轴突沿着MHB走行。一个意外的结果是,神经纤毛蛋白2的错误表达消除了中脑诱发的排斥反应,使滑车神经运动轴突能够穿过MHB并侵入顶盖。用神经纤毛蛋白2胞外域进行的结合试验揭示了中脑中存在神经纤毛蛋白2配体,这些配体被异位表达的神经纤毛蛋白2所掩盖。因此,我们提出神经纤毛蛋白2中和排斥活性,以便将滑车神经运动轴突引向背侧交叉点。综上所述,我们的结果表明神经纤毛蛋白2与其配体的相互作用对于沿MHB建立滑车神经轨迹起着关键作用。