Giniger Edward
Division of Basic Sciences, Program in Developmental Biology, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave, N, Seattle, WA 98109-1024, USA.
Differentiation. 2002 Oct;70(8):385-96. doi: 10.1046/j.1432-0436.2002.700801.x.
For a neuron to play its assigned role in a neural circuit, it has to extend elaborate projections, dendrites and axons, to make precise connections with specific target cells. The past decade has seen the identification of a vast diversity of molecules that assist in the guidance of axons toward their intended targets: guidance cues, growth cone receptors, signaling proteins (Tessier-Lavigne and Goodman, 1996; Song and Poo, 2001). But just how do all of these proteins work together to cause the axon to grow, stop, or turn in a specific direction? In this review, we examine this process from several different perspectives - cytoskeletal dynamics; biochemistry of intracellular signaling proteins; molecular analysis of axon guidance receptors - to try to collapse some of the apparent complexity of axon guidance into a more coherent picture. In particular, we will see how relatively simple and consistent manipulations of the kinetic constants of Rho family GTPases could account for many aspects of the cycle of actin dynamics that underlies axon growth and guidance. This review will intentionally be highly selective in its treatment of this subject in order to synthesize a simplified view that may be of value in directing further thinking and experiments.
为了使神经元在神经回路中发挥其指定作用,它必须延伸出精细的突起,即树突和轴突,以便与特定的靶细胞建立精确的连接。在过去十年中,人们已经鉴定出大量有助于轴突导向其预定靶标的分子:导向线索、生长锥受体、信号蛋白(Tessier-Lavigne和Goodman,1996;Song和Poo,2001)。但是,所有这些蛋白质究竟是如何协同作用,使轴突生长、停止或转向特定方向的呢?在这篇综述中,我们从几个不同的角度来审视这个过程——细胞骨架动力学;细胞内信号蛋白的生物化学;轴突导向受体的分子分析——试图将轴突导向的一些明显复杂性整合成一个更连贯的图景。特别是,我们将看到对Rho家族GTP酶动力学常数进行相对简单且一致的调控,如何能够解释构成轴突生长和导向基础的肌动蛋白动力学循环的许多方面。这篇综述将有意高度选择性地论述这个主题,以便综合出一个简化的观点,这可能对指导进一步的思考和实验有价值。