Drerup Catherine M, Lusk Sarah, Nechiporuk Alex
Department of Cell, Developmental, & Cancer Biology, Oregon Health & Science University, Portland, Oregon 97239
Department of Cell, Developmental, & Cancer Biology, Oregon Health & Science University, Portland, Oregon 97239.
J Neurosci. 2016 Jun 29;36(26):7014-26. doi: 10.1523/JNEUROSCI.0054-16.2016.
Delivery of proteins and organelles to the growth cone during axon extension relies on anterograde transport by kinesin motors. Though critical for neural circuit development, the mechanisms of cargo-specific anterograde transport during axon extension are only starting to be explored. Cargos of particular importance for axon outgrowth are microtubule modifiers, such as SCG10 (Stathmin-2). SCG10 is expressed solely during axon extension, localized to growth cones, and essential for axon outgrowth; however, the mechanisms of SCG10 transport and activity were still debated. Using zebrafish mutants and in vivo imaging, we identified the Kif1B motor and its interactor Kif1 binding protein (KBP) as critical for SCG10 transport to axon growth cones and complete axon extension. Axon truncation in kbp(st23) mutants can be suppressed by SCG10 overexpression, confirming the direct relationship between decreased SCG10 levels and failed axon outgrowth. Live imaging revealed that the reduced levels of SCG10 in kbp(st23) mutant growth cones led to altered microtubule stability, defining the mechanistic basis of axon truncation. Thus, our data reveal a novel role for the Kif1B-KBP complex in the anterograde transport of SCG10, which is necessary for proper microtubule dynamics and subsequent axon extension.
Together, our data define the mechanistic underpinnings of failed axon outgrowth with loss of KBP or its associated motor, Kif1B. In addition, we provide conclusive evidence that this defect results from disruption of anterograde transport of SCG10. This is one of the first examples of a motor to be implicated in the essential transport of a discreet cargo necessary for axon extension. In addition, counter to previous in vitro and cell culture results, neither loss of the Kif1B motor nor KBP resulted in inhibition of mitochondrial transport. Altogether, our work links transport of SCG10 to the regulation of microtubule dynamics in the axon growth cone and enhances our understanding of this process during axon outgrowth.
在轴突延伸过程中,蛋白质和细胞器向生长锥的运输依赖于驱动蛋白的顺行运输。尽管这对神经回路发育至关重要,但轴突延伸过程中货物特异性顺行运输的机制才刚刚开始被探索。对轴突生长特别重要的货物是微管修饰剂,如SCG10(Stathmin-2)。SCG10仅在轴突延伸期间表达,定位于生长锥,对轴突生长至关重要;然而,SCG10运输和活性的机制仍存在争议。利用斑马鱼突变体和体内成像,我们确定驱动蛋白Kif1B及其相互作用蛋白Kif1结合蛋白(KBP)对SCG10运输到轴突生长锥和完整的轴突延伸至关重要。kbp(st23)突变体中的轴突截断可以通过SCG10过表达来抑制,证实了SCG10水平降低与轴突生长失败之间的直接关系。实时成像显示,kbp(st23)突变体生长锥中SCG10水平的降低导致微管稳定性改变,确定了轴突截断的机制基础。因此,我们的数据揭示了Kif1B-KBP复合物在SCG10顺行运输中的新作用,这对适当的微管动力学和随后的轴突延伸是必需的。
总之,我们的数据定义了因KBP或其相关驱动蛋白Kif1B缺失而导致轴突生长失败的机制基础。此外,我们提供了确凿的证据,证明这种缺陷是由SCG10顺行运输的破坏引起的。这是驱动蛋白参与轴突延伸所需特定货物的基本运输的首批例子之一。此外,与之前的体外和细胞培养结果相反,Kif1B驱动蛋白或KBP的缺失均未导致线粒体运输受到抑制。总之,我们的工作将SCG10的运输与轴突生长锥中微管动力学的调节联系起来,并增强了我们对轴突生长过程中这一过程的理解。