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

被引:625
作者
Maruyama, Masahiro [1 ]
Shimada, Hitoshi [1 ]
Suhara, Tetsuya [1 ]
Shinotoh, Hitoshi [1 ]
Ji, Bin [1 ]
Maeda, Jun [1 ]
Zhang, Ming-Rong [1 ]
Trojanowski, John Q. [2 ]
Lee, Virginia M. -Y. [2 ]
Ono, Maiko [1 ]
Masamoto, Kazuto [1 ]
Takano, Harumasa [1 ]
Sahara, Naruhiko [3 ,5 ,6 ]
Iwata, Nobuhisa [4 ]
Okamura, Nobuyuki [7 ]
Furumoto, Shozo [7 ]
Kudo, Yukitsuka [8 ]
Chang, Qing [9 ]
Saido, Takaomi C. [4 ]
Takashima, Akihiko [3 ]
Lewis, Jada [5 ,6 ]
Jang, Ming-Kuei [9 ]
Aoki, Ichio [1 ]
Ito, Hiroshi [1 ]
Higuchi, Makoto [1 ]
机构
[1] Natl Inst Radiol Sci, Mol Imaging Ctr, Inage Ku, Chiba 2638555, Japan
[2] Univ Penn, Perelman Sch Med, Ctr Neurodegenerat Dis Res, Philadelphia, PA 19104 USA
[3] RIKEN Brain Sci Inst, Lab Alzheimers Dis, Wako, Saitama 3510198, Japan
[4] RIKEN Brain Sci Inst, Lab Proteolyt Neurosci, Wako, Saitama 3510198, Japan
[5] Univ Florida, Ctr Translat Res Neurodegenerat Dis, Gainesville, FL 32610 USA
[6] Univ Florida, Dept Neurosci, Gainesville, FL 32610 USA
[7] Tohoku Univ, Grad Sch Med, Dept Pharmacol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[8] Tohoku Univ Hosp, Clin Res Innovat & Educ Ctr, Aoba Ku, Sendai, Miyagi 9808574, Japan
[9] Univ Texas MD Anderson Canc Ctr, Inst Appl Canc Sci, Houston, TX 77054 USA
基金
美国国家卫生研究院;
关键词
IN-VIVO DETECTION; AMYLOID-BETA; DISEASE; PET; BINDING; DISORDERS; PLAQUES; TANGLES; LIGAND; TRACER;
D O I
10.1016/j.neuron.2013.07.037
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
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, [C-11]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, [C-11]Pittsburgh Compound-B ([C-11]PIB. [C-11]PBB3-PET data were also consistent with the spreading of tau pathology with AD progression. Furthermore, increased [C-11]PBB3 signals were found in a corticobasal syndrome patient negative for [C-11]PIB-PET.
引用
收藏
页码:1094 / 1108
页数:15
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