Increased Cerebral Level of P2X7R in a Tauopathy Mouse Model by PET Using [18F]GSK1482160

被引:2
|
作者
Kong, Yanyan [1 ]
Cao, Lei [1 ,2 ]
Wang, Jiao [3 ]
Zhuang, Junyi [3 ]
Liu, Yongshan [4 ]
Bi, Lei [4 ]
Qiu, Yifan [4 ]
Hou, Yuyi [4 ]
Huang, Qi [1 ]
Xie, Fang [1 ]
Yang, Yunhao [1 ]
Shi, Kuangyu [5 ]
Rominger, Axel [5 ]
Guan, Yihui [1 ]
Jin, Hongjun [4 ]
Ni, Ruiqing [2 ,5 ,6 ,7 ]
机构
[1] Fudan Univ, Huashan Hosp, PET Ctr, Shanghai 200235, Peoples R China
[2] Univ Zurich, Inst Regenerat Med, CH-8952 Zurich, Switzerland
[3] Shanghai Univ, Sch Life Sci, Lab Mol Neural Biol, Shanghai 200444, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 5, Guangdong Prov Engn Res Ctr Mol Imaging, Zhuhai 519000, Guangdong, Peoples R China
[5] Univ Hosp Bern, Dept Nucl Med, Inselspital, CH-3010 Bern, Switzerland
[6] Univ Zurich, Inst Biomed Engn, CH-8093 Zurich, Switzerland
[7] Swiss Fed Inst Technol, Zurich, Switzerland
来源
ACS CHEMICAL NEUROSCIENCE | 2024年 / 15卷 / 11期
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
Alzheimer's disease; amyloid-beta; glia; PET; tau; P2X(7) RECEPTOR ANTAGONIST; ALZHEIMERS-DISEASE; IN-VIVO; AMYLOID PLAQUES; BETA; TRACER; NEUROINFLAMMATION; EXPRESSION; MICE;
D O I
10.1021/acschemneuro.4c00067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neuroinflammation plays an important role in Alzheimer's disease and primary tauopathies. The aim of the current study was to map [F-18]GSK1482160 for imaging of purinergic P2X7R in Alzheimer's disease and primary tauopathy mouse models. Small animal PET was performed using [F-18]GSK1482160 in widely used mouse models of Alzheimer's disease (APP/PS1, 5xFAD, and 3xTg), 4-repeat tauopathy (rTg4510) mice, and age-matched wild-type mice. Increased uptake of [F-18]GSK1482160 was observed in the brains of 7-month-old rTg4510 mice compared to wild-type mice and compared to 3-month-old rTg4510 mice. A positive correlation between hippocampal tau [F-18]APN-1607 and [F-18]GSK1482160 uptake was found in rTg4510 mice. No significant differences in the uptake of [F-18]GSK1482160 was observed for APP/PS1 mice, 5xFAD mice, or 3xTg mice. Immunofluorescence staining further indicated the distribution of P2X7Rs in the brains of 7-month-old rTg4510 mice with accumulation of tau inclusion. These findings provide in vivo imaging evidence for an increased level of P2X7R in the brains of tauopathy mice.
引用
收藏
页码:2112 / 2120
页数:9
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