Edwards Tyson J, Hammarlund Marc
Department of Genetics, Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, BCMM 436E, 295 Congress Avenue, New Haven, CT 06510, USA.
Department of Genetics, Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, BCMM 436E, 295 Congress Avenue, New Haven, CT 06510, USA.
Cell Rep. 2014 Jul 10;8(1):272-83. doi: 10.1016/j.celrep.2014.06.008. Epub 2014 Jul 4.
Growth cones facilitate the repair of nervous system damage by providing the driving force for axon regeneration. Using single-neuron laser axotomy and in vivo time-lapse imaging, we show that syndecan, a heparan sulfate (HS) proteoglycan, is required for growth cone function during axon regeneration in C. elegans. In the absence of syndecan, regenerating growth cones form but are unstable and collapse, decreasing the effective growth rate and impeding regrowth to target cells. We provide evidence that syndecan has two distinct functions during axon regeneration: (1) a canonical function in axon guidance that requires expression outside the nervous system and depends on HS chains and (2) an intrinsic function in growth cone stabilization that is mediated by the syndecan core protein, independently of HS. Thus, syndecan is a regulator of a critical choke point in nervous system repair.
生长锥通过为轴突再生提供驱动力来促进神经系统损伤的修复。利用单神经元激光轴突切断术和体内延时成像技术,我们发现,在秀丽隐杆线虫轴突再生过程中,硫酸乙酰肝素蛋白聚糖syndecan是生长锥功能所必需的。在缺乏syndecan的情况下,再生生长锥虽能形成,但不稳定且会塌陷,从而降低有效生长速率并阻碍向靶细胞的再生长。我们提供的证据表明,syndecan在轴突再生过程中具有两种不同的功能:(1)在轴突导向中的经典功能,这需要在神经系统外表达且依赖于硫酸乙酰肝素链;(2)在生长锥稳定中的内在功能,这由syndecan核心蛋白介导,独立于硫酸乙酰肝素。因此,syndecan是神经系统修复中一个关键瓶颈点的调节因子。