Department of Neurosurgery, Penn Center for Brain Injury and Repair, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
The Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA.
Brain Pathol. 2019 May;29(3):437-450. doi: 10.1111/bpa.12677. Epub 2018 Dec 27.
Diffuse axonal injury (DAI) is an important consequence of traumatic brain injury (TBI). At the moment of trauma, axons rarely disconnect, but undergo cytoskeletal disruption and transport interruption leading to protein accumulation within swellings. The amyloid precursor protein (APP) accumulates rapidly and the standard histological evaluation of axonal pathology relies upon its detection. APP+ swellings first appear as varicosities along intact axons, which can ultimately undergo secondary disconnection to leave a terminal "axon bulb" at the disconnected, proximal end. However, sites of disconnection are difficult to determine with certainty using standard, thin tissue sections, thus limiting the comprehensive evaluation of axon degeneration. The tissue-clearing technique, CLARITY, permits three-dimensional visualization of axons that would otherwise be out of plane in standard tissue sections. Here, we examined the morphology and connection status of APP+ swellings using CLARITY at 6 h, 24 h, 1 week and 1 month following the controlled cortical impact (CCI) model of TBI in mice. Remarkably, many APP+ swellings that appeared as terminal bulbs when viewed in standard 8-µm-thick regions of tissue were instead revealed to be varicose swellings along intact axons when three dimensions were fully visible. Moreover, the percentage of these potentially viable axon swellings differed with survival from injury and may represent the delayed onset of distinct mechanisms of degeneration. Even at 1-month post-CCI, ~10% of apparently terminal bulbs were revealed as connected by CLARITY and are thus potentially salvageable. Intriguingly, the diameter of swellings decreased with survival, including varicosities along intact axons, and may reflect reversal of, or reduced, axonal transport interruption in the chronic setting. These data indicate that APP immunohistochemistry on standard thickness tissue sections overestimates axon disconnection, particularly acutely post-injury. Evaluating cleared tissue demonstrates a surprisingly delayed process of axon disconnection and thus longer window of therapeutic opportunity than previously appreciated. Intriguingly, a subset of axon swellings may also be capable of recovery.
弥漫性轴索损伤(DAI)是创伤性脑损伤(TBI)的重要后果。在创伤时刻,轴突很少断开,但会发生细胞骨架破坏和运输中断,导致肿胀内的蛋白质积累。淀粉样前体蛋白(APP)迅速积累,轴突病理学的标准组织学评估依赖于其检测。APP+肿胀首先出现在完整轴突上的膨大体中,这些膨大体最终可能会经历二次断开,从而在断开的近端留下一个末端“轴突球”。然而,使用标准的薄组织切片很难确定断开的部位,因此限制了对轴突退化的全面评估。组织清除技术 CLARITY 允许对标准组织切片中不在平面内的轴突进行三维可视化。在这里,我们在小鼠受控皮质撞击(CCI)TBI 模型后 6 小时、24 小时、1 周和 1 个月使用 CLARITY 检查了 APP+肿胀的形态和连接状态。值得注意的是,当在标准 8 µm 厚的组织区域观察时,许多作为末端球出现的 APP+肿胀实际上被证明是完整轴突上的曲张肿胀,当完全可见三维时。此外,这些潜在存活的轴突肿胀的百分比因损伤后的存活而不同,并且可能代表不同退化机制的延迟发作。即使在 CCI 后 1 个月,通过 CLARITY 发现约 10%的明显末端球仍然相连,因此具有潜在的可挽救性。有趣的是,肿胀的直径随存活时间而减小,包括完整轴突上的曲张肿胀,并且可能反映了慢性状态下轴突运输中断的逆转或减少。这些数据表明,在标准厚度的组织切片上进行 APP 免疫组织化学染色会高估轴突断开,特别是在损伤后急性阶段。评估清除的组织表明,轴突断开的过程出乎意料地延迟,因此比以前认识到的治疗机会窗口更长。有趣的是,一部分轴突肿胀也可能具有恢复能力。