Li Xiaoling, Gao Xue, Liu Guofa, Xiong Wencheng, Wu Jane, Rao Yi
Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Nat Neurosci. 2008 Jan;11(1):28-35. doi: 10.1038/nn2022. Epub 2007 Dec 9.
Netrins are prototypical axon guidance cues whose attractive signaling requires the small GTPase Rac1. It remains unclear how Rac1 is regulated in the netrin pathway. DOCK180 is a member of a new family of guanine nucleotide exchange factors for Rho GTPases. Here we provide evidence implicating DOCK180 in netrin signal transduction. Netrin promoted the formation of a protein-protein interaction complex that included DOCK180 and the netrin receptor deleted in colorectal carcinoma (DCC). Inhibition of DOCK180 reduced activation of Rac1 by netrin. Both axon outgrowth and axon attraction induced by netrin were inhibited after DOCK180 knockdown in vertebrate neurons. The in vivo functional role of DOCK180 was demonstrated by its requirement for projection of commissural axons in the neural tube. These findings indicate that netrin stimulation recruits DOCK180 through DCC, which then activates small GTPases, suggesting an essential role for DOCK180 in mediating attractive responses by neurons to netrin-1.
Netrins是典型的轴突导向因子,其吸引信号传导需要小GTP酶Rac1。目前尚不清楚Rac1在netrin信号通路中是如何被调控的。DOCK180是Rho GTP酶鸟嘌呤核苷酸交换因子新家族的成员。在此,我们提供了DOCK180参与netrin信号转导的证据。Netrin促进了一种蛋白质-蛋白质相互作用复合物的形成,该复合物包括DOCK180和在结直肠癌中缺失的netrin受体(DCC)。抑制DOCK180可降低netrin对Rac1的激活。在脊椎动物神经元中敲低DOCK180后,netrin诱导的轴突生长和轴突吸引均受到抑制。DOCK180在神经管中对连合轴突投射的需求证明了其在体内的功能作用。这些发现表明,netrin刺激通过DCC招募DOCK180,然后激活小GTP酶,这表明DOCK180在介导神经元对netrin-1的吸引反应中起重要作用。