Imaging of Tau Pathology in a Tauopathy Mouse Model and in Alzheimer Patients Compared to Normal Controls

نویسندگان

  • Masahiro Maruyama
  • Hitoshi Shimada
  • Tetsuya Suhara
  • Hitoshi Shinotoh
  • Bin Ji
  • Jun Maeda
  • Ming-Rong Zhang
  • John Q. Trojanowski
  • Virginia M.-Y. Lee
  • Maiko Ono
  • Kazuto Masamoto
  • Harumasa Takano
  • Naruhiko Sahara
  • Nobuhisa Iwata
  • Nobuyuki Okamura
  • Shozo Furumoto
  • Yukitsuka Kudo
  • Qing Chang
  • Takaomi C. Saido
  • Akihiko Takashima
  • Jada Lewis
  • Ming-Kuei Jang
  • Ichio Aoki
  • Hiroshi Ito
  • Makoto Higuchi
چکیده

Accumulation of intracellular tau fibrils has been the focus of research on the mechanisms of neurodegeneration in Alzheimer's disease (AD) and related tauopathies. Here, we have developed a class of tau ligands, phenyl/pyridinyl-butadienyl-benzothiazoles/benzothiazoliums (PBBs), for visualizing diverse tau inclusions in brains of living patients with AD or non-AD tauopathies and animal models of these disorders. In vivo optical and positron emission tomographic (PET) imaging of a transgenic mouse model demonstrated sensitive detection of tau inclusions by PBBs. A pyridinated PBB, [(11)C]PBB3, was next applied in a clinical PET study, and its robust signal in the AD hippocampus wherein tau pathology is enriched contrasted strikingly with that of a senile plaque radioligand, [(11)C]Pittsburgh Compound-B ([(11)C]PIB). [(11)C]PBB3-PET data were also consistent with the spreading of tau pathology with AD progression. Furthermore, increased [(11)C]PBB3 signals were found in a corticobasal syndrome patient negative for [(11)C]PIB-PET.

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عنوان ژورنال:
  • Neuron

دوره 79  شماره 

صفحات  -

تاریخ انتشار 2013