The recognized incidence and pathological impact of traumatic brain injury (TBI) has increased tremendously in recent year. In particular the causal links between TBI and chronic traumatic encephalopathy (CTE) are becoming better understood. Many of the pathological hallmarks of Alzheimer's disease (AD) are shared with early changes in TBI and with the pathology of CTE. Of note are the rapid elevations of the amyloid-beta (A?) peptide after TBI and the accumulation of A? in relation to CTE. Considering the importance of A? to AD, it is reasonable to implicate this peptide in the response to TBI and the development of CTE. Natural mechanisms of clearance of A? are important in the progression of AD and so these clearance mechanisms may also be important in TBI/CTE. Of note are the A?-degrading enzymes neprilysin (NEP) and its homolog neprilysin-2 (NEP2) which are important for controlling cerebral A? levels. Therefore, we propose a role for these enzymes in TBI/CTE. The central hypothesis is that NEP or NEP2 expression is important for effective recovery after TBI and protects from the development of CTE.
In Aim 1, we will test this hypothesis through the use of NEP and NEP2 knockout as well as NEP transgenic mice which will receive mild-repetitive or single severe TBI, after which they will be assessed for neurological function and pathology acutely after injury. We predict that the lack of NEP or NEP2 will exacerbate aspects of acute pathology after injury while NEP overproduction will ameliorate pathology.
In Aim 2 we will test for the effects of NEP or NEP2 alterations on chronic development of CTE-like pathology months after injury involving multiple mild or single severe TBI. In this aim we expect that decreased NEP or NEP2 will exacerbate, while increased NEP will protect against aspects of CTE-like pathology (learning and memory deficits, anxiety) in our models. This work is innovative because the effects of reduced or enhanced NEP-like expression on the progression of TBI and CTE have not been addressed. Also, the role of the NEP/NEP2 substrate, A?, in TBI and CTE is also not yet fully understood, and this project will investigate an alternate means of manipulating A? levels without altering APP and BACE1 or using secretase inhibitors. These experiments will shed light on the role of these A?-degrading endopeptidases in TBI and CTE allowing for the potential development of therapies based on augmenting their activity post injury. Furthermore, this work could help in identifying gene expression markers that predict outcome after TBI.

Public Health Relevance

This proposal will utilize NEP / NEP2 knockout and NEP transgenic mice expressing human APP to investigate the role of these amyloid-beta degrading enzymes in the response to traumatic brain injury (TBI) and the subsequent development of chronic traumatic encephalopathy (CTE). This work may identify biological markers and therapeutic targets for TBI/CTE and further examine the role of A? in these processes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21NS093570-01A1
Application #
9111194
Study Section
Brain Injury and Neurovascular Pathologies Study Section (BINP)
Program Officer
Bellgowan, Patrick S F
Project Start
2016-08-01
Project End
2018-05-31
Budget Start
2016-08-01
Budget End
2017-05-31
Support Year
1
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Rosalind Franklin University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
069501252
City
North Chicago
State
IL
Country
United States
Zip Code
60064