TY - JOUR
T1 - Rapid accumulation of endogenous Tau oligomers in a rat model of traumatic brain injury
T2 - Possible link between traumatic brain injury and sporadic tauopathies
AU - Hawkins, Bridget E.
AU - Krishnamurthy, Shashirekha
AU - Castillo-Carranza, Diana L.
AU - Sengupta, Urmi
AU - Prough, Donald S.
AU - Jackson, George R.
AU - DeWitt, Douglas S.
AU - Kayed, Rakez
PY - 2013/6/7
Y1 - 2013/6/7
N2 - Traumatic brain injury (TBI) is a serious problem that affects millions of people in the United States alone. Multiple concussions or even a single moderate to severe TBI can also predispose individuals to develop a pathologically distinct form of tauopathy-related dementia at an early age. No effective treatments are currently available for TBI or TBI-related dementia; moreover, only recently has insight been gained regarding the mechanisms behind their connection. Here, we used antibodies to detect oligomeric and phosphorylated Tau proteins in a non-transgenic rodent model of parasagittal fluid percussion injury. Oligomeric and phosphorylated Tau proteins were detected 4 and 24 h and 2 weeks post-TBI in injured, but not sham control rats. These findings suggest that diagnostic tools and therapeutics that target only toxic forms of Tau may provide earlier detection and safe, more effective treatments for tauopathies associated with repetitive neurotrauma.
AB - Traumatic brain injury (TBI) is a serious problem that affects millions of people in the United States alone. Multiple concussions or even a single moderate to severe TBI can also predispose individuals to develop a pathologically distinct form of tauopathy-related dementia at an early age. No effective treatments are currently available for TBI or TBI-related dementia; moreover, only recently has insight been gained regarding the mechanisms behind their connection. Here, we used antibodies to detect oligomeric and phosphorylated Tau proteins in a non-transgenic rodent model of parasagittal fluid percussion injury. Oligomeric and phosphorylated Tau proteins were detected 4 and 24 h and 2 weeks post-TBI in injured, but not sham control rats. These findings suggest that diagnostic tools and therapeutics that target only toxic forms of Tau may provide earlier detection and safe, more effective treatments for tauopathies associated with repetitive neurotrauma.
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U2 - 10.1074/jbc.M113.472746
DO - 10.1074/jbc.M113.472746
M3 - Article
C2 - 23632019
AN - SCOPUS:84878750229
SN - 0021-9258
VL - 288
SP - 17042
EP - 17050
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 23
ER -