Ng Julian, Luo Liqun
Department of Biological Sciences, Stanford University, Stanford, CA 94305, USA.
Neuron. 2004 Dec 2;44(5):779-93. doi: 10.1016/j.neuron.2004.11.014.
Rho GTPases are essential regulators of cytoskeletal reorganization, but how they do so during neuronal morphogenesis in vivo is poorly understood. Here we show that the actin depolymerization factor cofilin is essential for axon growth in Drosophila neurons. Cofilin function in axon growth is inhibited by LIM kinase and activated by Slingshot phosphatase. Dephosphorylating cofilin appears to be the major function of Slingshot in regulating axon growth in vivo. Genetic data provide evidence that Rho or Rac/Cdc42, via effector kinases Rok or Pak, respectively, activate LIM kinase to inhibit axon growth. Importantly, Rac also activates a Pak-independent pathway that promotes axon growth, and different RacGEFs regulate these distinct pathways. These genetic analyses reveal convergent and divergent pathways from Rho GTPases to the cytoskeleton during axon growth in vivo and suggest that different developmental outcomes could be achieved by biases in pathway selection.
Rho GTP酶是细胞骨架重组的关键调节因子,但它们在体内神经元形态发生过程中如何发挥作用却知之甚少。在这里,我们表明肌动蛋白解聚因子丝切蛋白对果蝇神经元的轴突生长至关重要。丝切蛋白在轴突生长中的功能受到LIM激酶的抑制,并被弹弓磷酸酶激活。去磷酸化丝切蛋白似乎是弹弓在体内调节轴突生长的主要功能。遗传数据表明,Rho或Rac/Cdc42分别通过效应激酶Rok或Pak激活LIM激酶以抑制轴突生长。重要的是,Rac还激活了一条不依赖Pak的促进轴突生长的途径,并且不同的Rac鸟嘌呤核苷酸交换因子调节这些不同的途径。这些遗传分析揭示了在体内轴突生长过程中从Rho GTP酶到细胞骨架的汇聚和发散途径,并表明通过途径选择的偏差可以实现不同的发育结果。