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- W2802649373 abstract "Several studies have now supported the use of a tau lowering agent as a possible therapy in the treatment of tauopathy disorders, including Alzheimer's disease. In human Alzheimer's disease, however, concurrent amyloid-β deposition appears to synergize and accelerate tau pathological changes. Thus far, tau reduction strategies that have been tested in vivo have been examined in the setting of tau pathology without confounding amyloid-β deposition. To determine whether reducing total human tau expression in a transgenic model where there is concurrent amyloid-β plaque formation can still reduce tau pathology and protect against neuronal loss, we have taken advantage of the regulatable tau transgene in APP/PS1 × rTg4510 mice. These mice develop both neurofibrillary tangles as well as amyloid-β plaques throughout the cortex and hippocampus. By suppressing human tau expression for 6 months in the APP/PS1 × rTg4510 mice using doxycycline, AT8 tau pathology, bioactivity, and astrogliosis were reduced, though importantly to a lesser extent than lowering tau in the rTg4510 alone mice. Based on non-denaturing gels and proteinase K digestions, the remaining tau aggregates in the presence of amyloid-β exhibit a longer-lived aggregate conformation. Nonetheless, lowering the expression of the human tau transgene was sufficient to equally ameliorate thioflavin-S positive tangles and prevent neuronal loss equally well in both the APP/PS1 × rTg4510 mice and the rTg4510 cohort. Together, these results suggest that, although amyloid-β stabilizes tau aggregates, lowering total tau levels is still an effective strategy for the treatment of tau pathology and neuronal loss even in the presence of amyloid-β deposition." @default.
- W2802649373 created "2018-05-17" @default.
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- W2802649373 date "2018-05-03" @default.
- W2802649373 modified "2023-10-16" @default.
- W2802649373 title "Tau reduction in the presence of amyloid-β prevents tau pathology and neuronal death in vivo" @default.
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- W2802649373 cites W1841850981 @default.
- W2802649373 cites W1965709917 @default.
- W2802649373 cites W1966312717 @default.
- W2802649373 cites W1968937229 @default.
- W2802649373 cites W1975141413 @default.
- W2802649373 cites W1977846417 @default.
- W2802649373 cites W1978445259 @default.
- W2802649373 cites W1980842500 @default.
- W2802649373 cites W1984009511 @default.
- W2802649373 cites W1984766678 @default.
- W2802649373 cites W1985259299 @default.
- W2802649373 cites W2011029903 @default.
- W2802649373 cites W2014526423 @default.
- W2802649373 cites W2015522247 @default.
- W2802649373 cites W2021069327 @default.
- W2802649373 cites W2021753155 @default.
- W2802649373 cites W2022532556 @default.
- W2802649373 cites W2030317956 @default.
- W2802649373 cites W2030602441 @default.
- W2802649373 cites W2030813189 @default.
- W2802649373 cites W2039314393 @default.
- W2802649373 cites W2046847750 @default.
- W2802649373 cites W2052742260 @default.
- W2802649373 cites W2053460912 @default.
- W2802649373 cites W2056079743 @default.
- W2802649373 cites W2056426612 @default.
- W2802649373 cites W2059809766 @default.
- W2802649373 cites W2060004104 @default.
- W2802649373 cites W2062772621 @default.
- W2802649373 cites W2064963539 @default.
- W2802649373 cites W2073391734 @default.
- W2802649373 cites W2073724760 @default.
- W2802649373 cites W2074274706 @default.
- W2802649373 cites W2075366433 @default.
- W2802649373 cites W2076333797 @default.
- W2802649373 cites W2076482846 @default.
- W2802649373 cites W2081966615 @default.
- W2802649373 cites W2082429191 @default.
- W2802649373 cites W2083799472 @default.
- W2802649373 cites W2088148170 @default.
- W2802649373 cites W2089215677 @default.
- W2802649373 cites W2100467035 @default.
- W2802649373 cites W2105704879 @default.
- W2802649373 cites W2106729121 @default.
- W2802649373 cites W2110888808 @default.
- W2802649373 cites W2111896974 @default.
- W2802649373 cites W2117926331 @default.
- W2802649373 cites W2118516203 @default.
- W2802649373 cites W2122582684 @default.
- W2802649373 cites W2126264983 @default.
- W2802649373 cites W2126974689 @default.
- W2802649373 cites W2135309154 @default.
- W2802649373 cites W2137959606 @default.
- W2802649373 cites W2138485921 @default.
- W2802649373 cites W2142943752 @default.
- W2802649373 cites W2149077867 @default.
- W2802649373 cites W2150771555 @default.
- W2802649373 cites W2155009321 @default.
- W2802649373 cites W2158766477 @default.
- W2802649373 cites W2206932523 @default.
- W2802649373 cites W2215407066 @default.
- W2802649373 cites W2222784460 @default.
- W2802649373 cites W2239308353 @default.
- W2802649373 cites W2469385416 @default.
- W2802649373 cites W2494872295 @default.
- W2802649373 cites W2531898330 @default.
- W2802649373 cites W2582711285 @default.
- W2802649373 cites W2599826853 @default.
- W2802649373 cites W2604266288 @default.
- W2802649373 cites W2612796913 @default.
- W2802649373 cites W2755784837 @default.
- W2802649373 cites W2766057155 @default.
- W2802649373 cites W2772451653 @default.
- W2802649373 cites W774647991 @default.
- W2802649373 doi "https://doi.org/10.1093/brain/awy117" @default.