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首页> 外文期刊>Brain pathology >CLARITY reveals a more protracted temporal course of axon swelling and disconnection than previously described following traumatic brain injury
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CLARITY reveals a more protracted temporal course of axon swelling and disconnection than previously described following traumatic brain injury

机译:清晰度揭示了轴突肿胀和断开的轴颈肿胀和断开的颞型肿胀,而不是在创伤性脑损伤以下描述

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摘要

Abstract 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.
机译:摘要弥漫性轴突损伤(DAI)是创伤性脑损伤(TBI)的重要结果。在创伤的那一刻,轴突很少断开,但经历细胞骨骼破坏和运输中断导致肿胀内的蛋白质积累。淀粉样蛋白前体蛋白(APP)迅速积累,并且轴突病理的标准组织学评估依赖于其检测。 App + Swellings首先沿着完整的轴突出现为芳级,这最终可能最终经历二次断开连接,以在断开连接的近端处留下终端“Axon灯泡”。然而,断开的部位难以使用标准,薄的组织切片确定确定,因此限制了轴突变性的综合评价。组织清洁技术清晰度,允许诸如标准组织部分中的平面中的轴突的三维可视化。在这里,我们使用在小鼠TBI的受控皮质撞击(CCI)模型之后使用6?H,24℃,1周和1个月的清晰度来检查APP +肿胀的形态和连接状态。值得注意的是,当在标准的8-μm厚的组织区域观察时,许多应用+肿胀被视为终端灯泡,当三个尺寸完全可见时,沿着完整的轴突被揭示为静脉曲张肿胀。此外,这些潜在可行的轴突膨胀的百分比与损伤的存活率不同,并且可以代表延迟的变性机制的延迟发作。即使在1个月的CCI后,〜10%的明显终端灯泡被透露为通过清楚起见,因此可能是潜在的挽救性的。有趣的是,肿胀的直径随着存活而降低,包括沿完整轴突的致血清,并且可以反映慢性环境中的逆转或减少的轴突运输中断。这些数据表明,在标准厚度组织部分上的应用免疫组织化学高估了轴突断开,特别是急性损伤后。评估清除组织展示了轴突断开的令人惊讶的延迟过程,从而更长的治疗机会窗口比以前欣赏。有趣的是,轴突肿胀的子集也能够恢复。

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