化学
陶氏病
紧身衣
体内
荧光
转基因小鼠
生物物理学
体外
离体
荧光寿命成像显微镜
老年斑
生物化学
阿尔茨海默病
转基因
病理
神经退行性变
生物
基因
物理
生物技术
医学
量子力学
疾病
作者
Tianxin Xie,Yuying Li,Chuan Tian,Chang Yuan,Bin Dai,Shubo Wang,Kaixiang Zhou,Jiaqi Liu,Hongwei Tan,Yi Liang,Jiapei Dai,Baian Chen,Mengchao Cui
标识
DOI:10.1021/acs.jmedchem.2c00859
摘要
Neurofibrillary tangles (NFTs), which are composed of abnormally hyperphosphorylated Tau, are one of the main pathologic hallmarks of Alzheimer's disease and other tauopathies. The fluorescent imaging probes currently used to target NFTs cannot distinguish them well from β-amyloid plaques, thus limiting their utility to diagnose diseases. Here, we developed a fused cycloheptatriene–BODIPY derivative (TNIR7-1A) that displays properties favorable for near-infrared (NIR) imaging with high affinity and specificity to NFTs in vitro. In addition, TNIR7-1A effectively penetrated the blood–brain barrier and clearly distinguished tauopathy in transgenic mice (rTg4510) from control mice using NIR fluorescence imaging in vivo. The sensitivity and specificity of TNIR7-1A for NFTs were confirmed ex vivo by fluorescence staining of the tauopathy mouse model, while molecular docking studies indicated that TNIR7-1A bound to NFTs through hydrophobic interactions. These results suggest that TNIR7-1A can act as a high-performance probe to detect NFTs in vitro and in vivo selectively.
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