Kentucky Spinal Cord Injury Research Center, University of Louisville, School of Medicine, Louisville, KY 40202, USA; Department of Neurological Surgery, University of Louisville, School of Medicine, Louisville, KY 40202, USA.
Department of Bioengineering, University of Louisville, School of Medicine, Louisville, KY 40202, USA.
Exp Neurol. 2020 May;327:113258. doi: 10.1016/j.expneurol.2020.113258. Epub 2020 Feb 24.
Spinal cord injury (SCI) induces a secondary degenerative response that causes the loss of spared axons and worsens neurological outcome. The complex molecular mechanisms that mediate secondary axonal degeneration remain poorly understood. To further our understanding of secondary axonal degeneration following SCI, we assessed the spatiotemporal dynamics of axonal spheroid and terminal bulb formation following a contusive SCI in real-time in vivo. Adult 6-8 week old Thy1YFP transgenic mice underwent a T12 laminectomy for acute imaging sessions or were implanted with a custom spinal cord imaging chamber for chronic imaging of the spinal cord. Two-photon excitation time-lapse microscopy was performed prior to a mild contusion SCI (30 kilodyne, IH Impactor) and at 1-4 h and 1-14 days post-SCI. We quantified the number of axonal spheroids, their size and distribution, the number of endbulbs, and axonal survival from 1 h to 14 days post-SCI. Our data reveal that the majority of axons underwent swelling and axonal spheroid formation acutely after SCI resulting in the loss of ~70% of axons by 1 day after injury. In agreement, the number of axonal spheroids rapidly increased at 1 h after SCI and remained significantly elevated up to 14 days after SCI. Furthermore, the distribution of axonal spheroids spread mediolaterally over time indicative of delayed secondary degenerative processes. In contrast, axonal endbulbs were relatively sparse and their numbers peaked at 1 day after injury. Intriguingly, axonal survival significantly increased at 7 and 14 days compared to 3 days after SCI revealing a potential endogenous axonal repair process that mirrors the known spontaneous functional recovery after SCI. In support, ~43% of tracked axonal spheroids resolved over the course of observation revealing their dynamic nature. Furthermore, axonal spheroids and endbulbs accumulated mitochondria and excessive tubulin polyglutamylation suggestive of disrupted axonal transport as a shared mechanism. Collectively, this study provides important insight into both degenerative and recoverable responses of axons following contusive SCI in real-time. Understanding how axons spontaneously recover after SCI will be an important avenue for future SCI research and may help guide future clinical trials.
脊髓损伤(SCI)会引发继发性退行性反应,导致受损轴突的丢失,并使神经功能预后恶化。介导继发性轴突退化的复杂分子机制仍知之甚少。为了进一步了解 SCI 后的继发性轴突退化,我们在体内实时评估了挫伤性 SCI 后轴突球和终末球形成的时空动态。成年 6-8 周大的 Thy1YFP 转基因小鼠接受 T12 椎板切除术进行急性成像,或植入定制的脊髓成像室进行脊髓的慢性成像。在轻度挫伤性 SCI(30 千达因,IH 冲击器)之前和 SCI 后 1-4 小时和 1-14 天进行双光子激发延时显微镜检查。我们从 SCI 后 1 小时到 14 天量化了轴突球的数量、大小和分布、终末球的数量和轴突存活。我们的数据显示,大多数轴突在 SCI 后急性肿胀并形成轴突球,导致 1 天后约 70%的轴突丢失。一致地,SCI 后 1 小时后轴突球的数量迅速增加,直到 SCI 后 14 天仍显著升高。此外,轴突球的分布随时间向中侧扩散,表明存在延迟的继发性退行性过程。相比之下,轴突终末球相对稀疏,数量在损伤后 1 天达到峰值。有趣的是,与 SCI 后 3 天相比,7 天和 14 天后轴突存活显著增加,表明存在潜在的内源性轴突修复过程,与 SCI 后已知的自发功能恢复相吻合。支持这一观点的是,在观察过程中约有 43%的跟踪轴突球得到解决,揭示了它们的动态性质。此外,轴突球和终末球积累了线粒体和过多的微管蛋白多聚谷氨酸化,表明轴突运输受阻是一种共同的机制。总的来说,这项研究实时提供了对挫伤性 SCI 后轴突退行性和可恢复性反应的重要见解。了解轴突在 SCI 后如何自发恢复将是未来 SCI 研究的一个重要途径,并可能有助于指导未来的临床试验。