Yoshimura Takeshi, Arimura Nariko, Kaibuchi Kozo
Department of Molecular Biology, Graduate School of Science, Institute for Advanced Research, Nagoya University, Aichi 464-8602, Japan.
J Neurosci. 2006 Oct 18;26(42):10626-30. doi: 10.1523/JNEUROSCI.3824-06.2006.
A mature neuron is typically polarized both structurally and functionally, with a single long axon and several dendrites. Neuronal polarity is essential for unidirectional signal flow from somata or dendrites to axons. The initial event in establishing a polarized neuron is the specification of a single axon. Early in neuronal development, one immature neurite becomes differentiated from other neurites to form an axon. Although studies in the past two decades have yielded a catalog of structural, molecular, and functional differences between axons and dendrites, we are only now beginning to understand the molecular mechanisms involved in the establishment of neuronal polarity. In the last few years, neuronal polarity-regulating molecules have been revealed. There are two major signaling cascades in neuronal polarization. Several groups, including ours, reported that the phosphatidylinositol 3-kinase (PI3-kinase)/Akt/glycogen synthase kinase-3beta (GSK-3beta)/collapsin response mediator protein-2 pathway is important for axon specification and elongation. Recent studies have revealed that the positive feedback loop composed of Rho family small GTPases and the Par3/Par6/atypical protein kinase C complex plays a role in the initial events of neuronal polarization downstream of PI3-kinase. Here, we discuss the roles of signaling molecules for axon specification.
成熟神经元通常在结构和功能上都是极化的,具有单一的长轴突和多个树突。神经元极性对于从胞体或树突到轴突的单向信号流动至关重要。建立极化神经元的初始事件是确定单一轴突。在神经元发育早期,一条未成熟的神经突与其他神经突区分开来形成轴突。尽管过去二十年的研究已经列出了轴突和树突之间结构、分子和功能上的差异清单,但我们直到现在才开始了解参与建立神经元极性的分子机制。在过去几年中,已经发现了调节神经元极性的分子。在神经元极化中有两个主要的信号级联反应。包括我们小组在内的几个研究团队报告说,磷脂酰肌醇3激酶(PI3激酶)/Akt/糖原合酶激酶-3β(GSK-3β)/塌陷反应介导蛋白-2途径对于轴突的确定和延长很重要。最近的研究表明,由Rho家族小GTP酶和Par3/Par6/非典型蛋白激酶C复合物组成的正反馈环在PI3激酶下游的神经元极化初始事件中起作用。在这里,我们讨论信号分子在轴突确定中的作用。