Department of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607, USA.
Institute of Molecular and Cellular Biology, National Taiwan University, Taipei, 10617, Taiwan.
Nat Commun. 2018 Nov 19;9(1):4842. doi: 10.1038/s41467-018-07291-x.
Two important biological events happen coincidently soon after nerve injury in the peripheral nervous system in C. elegans: removal of axon debris and initiation of axon regeneration. But, it is not known how these two events are co-regulated. Mutants of ced-1, a homolog of Draper and MEGF10, display defects in both events. One model is that those events could be related. But our data suggest that they are actually separable. CED-1 functions in the muscle-type engulfing cells in both events and is enriched in muscle protrusions in close contact with axon debris and regenerating axons. Its two functions occur through distinct biochemical mechanisms; extracellular domain-mediated adhesion for regeneration and extracellular domain binding-induced intracellular domain signaling for debris removal. These studies identify CED-1 in engulfing cells as a receptor in debris removal but as an adhesion molecule in neuronal regeneration, and have important implications for understanding neural circuit repair after injury.
在秀丽隐杆线虫的周围神经系统中,神经损伤后会同时发生两个重要的生物学事件:轴突碎片的清除和轴突再生的启动。但是,目前尚不清楚这两个事件是如何共同调节的。CED-1 是 Draper 和 MEGF10 的同源物,其突变体在这两个事件中都存在缺陷。一种模型是,这些事件可能是相关的。但我们的数据表明,它们实际上是可分离的。CED-1 在这两个事件中都在肌肉型吞噬细胞中发挥作用,并且在与轴突碎片和再生轴突紧密接触的肌肉突起中富集。它的两种功能通过不同的生化机制发生;细胞外结构域介导的再生黏附和细胞外结构域结合诱导的细胞内结构域信号传导用于碎片清除。这些研究确定吞噬细胞中的 CED-1 作为碎片清除的受体,但作为神经元再生的黏附分子,对理解损伤后神经回路的修复具有重要意义。