Yaron Avraham, Huang Pei-Hsin, Cheng Hwai-Jong, Tessier-Lavigne Marc
Department of Biological Sciences, Howard Hughes Medical Institute, Stanford University, Stanford, California 94305, USA.
Neuron. 2005 Feb 17;45(4):513-23. doi: 10.1016/j.neuron.2005.01.013.
The class 3 Semaphorins Sema3A and Sema3F are potent axonal repellents that cause repulsion by binding Neuropilin-1 and Neuropilin-2, respectively. Plexins are implicated as signaling coreceptors for the Neuropilins, but the identity of the Plexins that transduce Sema3A and Sema3F responses in vivo is uncertain. Here, we show that Plexin-A3 and -A4 are key determinants of these responses, through analysis of a Plexin-A3/Plexin-A4 double mutant mouse. Sensory and sympathetic neurons from the double mutant are insensitive to Sema3A and Sema3F in vitro, and defects in axonal projections in vivo correspond to those seen in Neuropilin-1 and -2 mutants. Interestingly, we found a differential requirement for these two Plexins: signaling via Neuropilin-1 is mediated principally by Plexin-A4, whereas signaling via Neuropilin-2 is mediated principally by Plexin-A3. Thus, Plexin-A3 and -A4 contribute to the specificity of axonal responses to class 3 Semaphorins.
3类信号素Sema3A和Sema3F是强效的轴突排斥因子,它们分别通过与神经纤毛蛋白-1和神经纤毛蛋白-2结合而引起排斥反应。丛状蛋白被认为是神经纤毛蛋白的信号共受体,但在体内转导Sema3A和Sema3F反应的丛状蛋白的身份尚不确定。在这里,我们通过对丛状蛋白-A3/丛状蛋白-A4双突变小鼠的分析表明,丛状蛋白-A3和-A4是这些反应的关键决定因素。来自双突变体的感觉神经元和交感神经元在体外对Sema3A和Sema3F不敏感,并且体内轴突投射的缺陷与在神经纤毛蛋白-1和-2突变体中看到的缺陷相对应。有趣的是,我们发现这两种丛状蛋白有不同的需求:通过神经纤毛蛋白-1的信号传导主要由丛状蛋白-A4介导,而通过神经纤毛蛋白-2的信号传导主要由丛状蛋白-A3介导。因此,丛状蛋白-A3和-A4有助于轴突对3类信号素反应的特异性。