CLARITY reveals a more protracted temporal course of axon swelling and disconnection than previously described following traumatic brain injury

• Published in: Brain pathology (Zurich, Switzerland) Switzerland), 2019-05, Vol.29 (3), p.437-450
• Main Authors: Weber, Maura T., Arena, John D., Xiao, Rui, Wolf, John A., Johnson, Victoria E.
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Amyloid beta-Protein Precursor - metabolism; Amyloid precursor protein; Animals; axon degeneration; axonal pathology; Axonal Transport; Axons; Axons - pathology; Brain; Brain - pathology; Brain Injuries - pathology; Brain Injuries, Traumatic - complications; Brain Injuries, Traumatic - physiopathology; Bulbs; CLARITY; Cortex; Cytoskeleton; Degeneration; diffuse axonal injury; Diffuse Axonal Injury - metabolism; Diffuse Axonal Injury - pathology; Disease Models, Animal; Disruption; Head injuries; Histological Techniques - methods; Immunohistochemistry; Immunohistochemistry - methods; Interruption; Male; Mice; Mice, Inbred Strains; Morphology; Neurodegeneration; Protein transport; Proteins; Survival; TBI; Transport; Traumatic brain injury
• ISSN: 1015-6305; 1750-3639
• DOI: 10.1111/bpa.12677

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.