Mounting evidence suggests that the long-term impact of traumatic brain injury (TBI) may be far worse than previously thought. A history of brain trauma increases an individual's risk of developing Alzheimer's disease (AD), and TBI can induce the rapid formation of amyloid-ss (Ass) plaques, a hallmark pathology of AD. Pioneering work from this grant has demonstrated that massive accumulations of amyloid precursor protein (APP) in damaged axons after TBI are accompanied by the very secretases that cleave APP to form Ass. Uniquely, this anabolic process occurs within the axonal membrane compartment of humans with TBI and in animal models of TBI. However, although this axonal process persists for years after TBI, the frequency of Ass plaques appears to diminish within months. This suggests that there is also a potential Ass catabolic process after TBI. Indeed, we have shown in preliminary data using multiple models that neprilysin, the primary Ass degrading enzyme, may have a key role in clearing Ass following injury. In addition, preliminary human studies demonstrate stunning evidence that Ass plaques reappear several years and even decades after TBI. From these collective data, we hypothesize that there is a long-term shifting balance between Ass anabolism and catabolism after TBI. Remarkably, through preliminary examination we also found the other hallmark pathology of AD, neurofibrillary tangles (NFTs), in long-term survivors of TBI. This is further supported by the demonstration of NFTs chronically following injury in our unique swine model. This finding represents a significant new avenue in the exploration of mechanisms linking TBI and AD and is the first demonstration that NFT formation occurs chronically following just a single TBI. For this application, we propose a molecules-to-man approach to determine evolving mechanisms of AD-like pathologies after TBI. Through our longstanding collaboration between investigators at the University of Pennsylvania and Glasgow, UK, we will investigate long-term neuropathological changes after TBI, using the world's only comprehensive TBI human brain archive. In parallel interactive studies, we will examine well-characterized experimental models at the in vivo and in vitro level to determine the cellular and molecular mechanisms of Ass plaque and NFT genesis. In addition, we will examine the effects of Ass reduction after injury in experimental models with a view to therapeutic intervention. Success of these studies will provide insight into mechanisms that convert a single TBI into a progressive neurodegenerative disease.

Public Health Relevance

By studying evolving axonal pathology after traumatic brain injury (TBI), we have uncovered novel mechanisms that may represent the link between TBI and the subsequent development of Alzheimer's disease (AD). In particular, we discovered evolving hallmark AD pathologies of amyloid production and deposition as well as the formation of neurofibrillary tangles after TBI. Here, we propose to examine how TBI may be transformed into a progressive neurodegenerative disease with pathologic features resembling AD.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS038104-14
Application #
8670778
Study Section
Acute Neural Injury and Epilepsy Study Section (ANIE)
Program Officer
Hicks, Ramona R
Project Start
1999-02-15
Project End
2015-05-31
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
14
Fiscal Year
2014
Total Cost
$425,521
Indirect Cost
$127,973
Name
University of Pennsylvania
Department
Neurosurgery
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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Johnson, Victoria E; Stewart, Janice E; Begbie, Finn D et al. (2013) Inflammation and white matter degeneration persist for years after a single traumatic brain injury. Brain 136:28-42
Zetterberg, Henrik; Smith, Douglas H; Blennow, Kaj (2013) Biomarkers of mild traumatic brain injury in cerebrospinal fluid and blood. Nat Rev Neurol 9:201-10
Smith, Douglas H; Johnson, Victoria E; Stewart, William (2013) Chronic neuropathologies of single and repetitive TBI: substrates of dementia? Nat Rev Neurol 9:211-21
Johnson, Victoria E; Stewart, William; Smith, Douglas H (2013) Axonal pathology in traumatic brain injury. Exp Neurol 246:35-43
Tang-Schomer, Min D; Johnson, Victoria E; Baas, Peter W et al. (2012) Partial interruption of axonal transport due to microtubule breakage accounts for the formation of periodic varicosities after traumatic axonal injury. Exp Neurol 233:364-72
Johnson, Victoria E; Stewart, William; Trojanowski, John Q et al. (2011) Acute and chronically increased immunoreactivity to phosphorylation-independent but not pathological TDP-43 after a single traumatic brain injury in humans. Acta Neuropathol 122:715-26
Cullen, D Kacy; Xu, Yongan; Reneer, Dexter V et al. (2011) Color changing photonic crystals detect blast exposure. Neuroimage 54 Suppl 1:S37-44
Browne, Kevin D; Chen, Xiao-Han; Meaney, David F et al. (2011) Mild traumatic brain injury and diffuse axonal injury in swine. J Neurotrauma 28:1747-55
Cullen, D Kacy; Browne, Kevin D; Xu, Yongan et al. (2011) Blast-induced color change in photonic crystals corresponds with brain pathology. J Neurotrauma 28:2307-18

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