Department of Neuroscience, University of Texas at Austin, Austin, Texas.
Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas.
J Neurosci Res. 2018 Jul;96(7):1223-1242. doi: 10.1002/jnr.24225. Epub 2018 Apr 16.
Complete severance of major peripheral mixed sensory-motor nerve proximally in a mammalian limb produces immediate loss of action potential conduction and voluntary behaviors mediated by the severed distal axonal segments. These severed distal segments undergo Wallerian degeneration within days. Denervated muscles atrophy within weeks. Slowly regenerating (∼1 mm/day) outgrowths from surviving proximal stumps that often nonspecifically reinnervate denervated targets produce poor, if any, restoration of lost voluntary behaviors. In contrast, in this study using completely transected female rat sciatic axons as a model system, we provide extensive morphometric, immunohistochemical, electrophysiological, and behavioral data to show that these adverse outcomes are avoided by microsuturing closely apposed axonal cut ends (neurorrhaphy) and applying a sequence of well-specified solutions, one of which contains polyethylene glycol (PEG). This "PEG-fusion" procedure within minutes reestablishes axoplasmic and axolemmal continuity and signaling by nonspecifically fusing (connecting) closely apposed open ends of severed motor and/or sensory axons at the lesion site. These PEG-fused axons continue to conduct action potentials and generate muscle action potentials and muscle twitches for months and do not undergo Wallerian degeneration. Continuously innervated muscle fibers undergo much less atrophy compared with denervated muscle fibers. Dramatic behavioral recovery to near-unoperated levels occurs within days to weeks, almost certainly by activating many central nervous system and peripheral nervous system synaptic and other plasticities, some perhaps to a greater extent than most neuroscientists would expect. Negative control transections in which neurorrhaphy and all solutions except the PEG-containing solution are applied produce none of these remarkably fortuitous outcomes observed for PEG-fusion.
哺乳动物肢体近端主要混合感觉运动神经完全切断后,会立即导致被切断的远端轴突段介导的动作电位传导和随意行为丧失。这些被切断的远端段在数天内发生 Wallerian 变性。去神经支配的肌肉在数周内萎缩。从存活的近端残端缓慢再生(每天约 1 毫米)的再生(生长)突起,通常是非特异性地重新支配去神经支配的靶标,导致失去的随意行为无法很好恢复,如果有恢复的话。相比之下,在这项使用完全横断的雌性大鼠坐骨神经轴突作为模型系统的研究中,我们提供了广泛的形态计量学、免疫组织化学、电生理学和行为学数据,表明通过将紧密贴合的轴突切割端(神经吻合术)微缝合并应用一系列特定的溶液(其中一种包含聚乙二醇(PEG))可以避免这些不良后果。这种“PEG 融合”程序在几分钟内通过非特异性地融合(连接)损伤部位紧密贴合的断端开放的运动和/或感觉轴突,重新建立轴浆和轴突膜的连续性和信号传递。这些 PEG 融合的轴突可以继续传导动作电位,并在数月内产生肌肉动作电位和肌肉抽搐,并且不会发生 Wallerian 变性。与去神经支配的肌肉纤维相比,连续支配的肌肉纤维萎缩程度要小得多。在几天到几周内,几乎可以恢复到接近未手术的水平,这很可能是通过激活许多中枢神经系统和周围神经系统的突触和其他可塑性,其中一些可能比大多数神经科学家预期的程度更大。在应用神经吻合术和除含 PEG 溶液之外的所有溶液的阴性对照横切中,没有观察到这些对 PEG 融合非常有利的结果。