In vivo detection of amyloid-β deposits by near-infrared imaging using an oxazine-derivative probe

被引:290
作者
Hintersteiner, M
Enz, A
Frey, P
Jaton, AL
Kinzy, W
Kneuer, R
Neumann, U
Rudin, M
Staufenbiel, M
Stoeckli, M
Wiederhold, KH
Gremlich, HU [1 ]
机构
[1] Novartis Inst Biomed Res, Discovery Technol, CH-4002 Basel, Switzerland
[2] Novartis Inst Biomed Res, Nervous Syst Dept, CH-4002 Basel, Switzerland
关键词
D O I
10.1038/nbt1085
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
As Alzheimer's disease pathogenesis is associated with the formation of insoluble aggregates of amyloid beta-peptide, approaches allowing the direct, noninvasive visualization of plaque growth in vivo would be beneficial for biomedical research. Here we describe the synthesis and characterization of the near-infrared fluorescence oxazine dye AOI987, which readily penetrates the intact blood-brain barrier and binds to amyloid plaques. Using near-infrared fluorescence imaging, we demonstrated specific interaction of AOI987 with amyloid plaques in APP23 transgenic mice in vivo, as confirmed by postmortem analysis of brain slices. Quantitative analysis revealed increasing fluorescence signal intensity with increasing plaque load of the animals, and significant binding of AOI987 was observed for APP23 transgenic mice aged 9 months and older. Thus, AOI987 is an attractive probe to noninvasively monitor disease progression in animal models of Alzheimer disease and to evaluate effects of potential Alzheimer disease drugs on the plaque load.
引用
收藏
页码:577 / 583
页数:7
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