Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
Center for C. elegans Anatomy, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Cell Rep. 2016 Feb 23;14(7):1673-1683. doi: 10.1016/j.celrep.2016.01.050. Epub 2016 Feb 11.
Axonal degeneration is a characteristic feature of neurodegenerative disease and nerve injury. Here, we characterize axonal degeneration in Caenorhabditis elegans neurons following laser-induced axotomy. We show that this process proceeds independently of the WLD(S) and Nmnat pathway and requires the axonal clearance machinery that includes the conserved transmembrane receptor CED-1/Draper, the adaptor protein CED-6, the guanine nucleotide exchange factor complex Crk/Mbc/dCed-12 (CED-2/CED-5/CED-12), and the small GTPase Rac1 (CED-10). We demonstrate that CED-1 and CED-6 function non-cell autonomously in the surrounding hypodermis, which we show acts as the engulfing tissue for the severed axon. Moreover, we establish a function in this process for CED-7, an ATP-binding cassette (ABC) transporter, and NRF-5, a lipid-binding protein, both associated with release of lipid-vesicles during apoptotic cell clearance. Thus, our results reveal the existence of a WLD(S)/Nmnat-independent axonal degeneration pathway, conservation of the axonal clearance machinery, and a function for CED-7 and NRF-5 in this process.
轴突变性是神经退行性疾病和神经损伤的特征。在这里,我们描述了激光诱导轴突切断后秀丽隐杆线虫神经元中的轴突变性。我们表明,这个过程独立于 WLD(S) 和 Nmnat 途径进行,需要包括保守的跨膜受体 CED-1/Draper、衔接蛋白 CED-6、鸟嘌呤核苷酸交换因子复合物 Crk/Mbc/dCed-12 (CED-2/CED-5/CED-12) 和小 GTPase Rac1 (CED-10) 的轴突清除机制。我们证明 CED-1 和 CED-6 在周围的真皮层中非自主发挥作用,真皮层被证明是被切断轴突的吞噬组织。此外,我们在这个过程中建立了 CED-7(一种 ATP 结合盒 (ABC) 转运蛋白)和 NRF-5(一种脂质结合蛋白)的功能,它们都与凋亡细胞清除过程中脂质小泡的释放有关。因此,我们的结果揭示了存在一种 WLD(S)/Nmnat 独立的轴突变性途径、轴突清除机制的保守性,以及 CED-7 和 NRF-5 在这个过程中的功能。