A novel kit for early diagnosis of Alzheimer's disease using a fluorescent nanoparticle imaging

被引:26
|
作者
Park, Jun Sung [1 ]
Kim, Sang Tae [2 ]
Kim, Sang Yun [2 ]
Jo, Min Gi [1 ]
Choi, Myeong Jun [3 ]
Kim, Myeong Ok [1 ]
机构
[1] GNU, Coll Nat Sci, Div Life Sci & Appl Life Sci BK21 Plus, Jinju 52802, South Korea
[2] Seoul Natl Univ, Bundang Hosp, Dept Neurol, Seongnam Si 13605, Gyeonggi Do, South Korea
[3] Phytos Inc, Res & Dev Ctr, Anyang Mega Valley 609,268, Anyang, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
AMYLOID-BETA; BIOMARKERS; THERAPY; NANOTECHNOLOGY; THERAPEUTICS; INFLAMMATION; METABOLISM; ANTIBODIES; PROTEIN; INJURY;
D O I
10.1038/s41598-019-49711-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alzheimer's disease (AD) is a progressive neurodegenerative disease and chronic illness with long preclinical phases and a long clinical duration. Until recently, a lack of potential therapeutic agents against AD was the primary focus of research, which resulted in less effort directed towards developing useful diagnostic approaches. In this study, we developed a WO2002/088706 kit that is composed of fluorescent nanoparticles for the early detection of AD. We provided a fluorescent nanoparticle for detecting markers and a kit for the early diagnosis of AD. The kit consists of a probe molecule comprising an oligonucleotide capable of detecting one or more AD-specific microRNAs (miRNAs) and biomarkers related to AD. Through screening, we selected miR-106b, miR-146b, miR-181a, miR-200a, miR-34a, miR-124b, miR-153, miR-155, A beta(1-)(42) monomer (mA beta), A beta(1-)(42) oligomer (oA beta), UCHL1, NLRP3, Tau, STAT3, SORL1, Clusterin, APOE3, APOE4, Nogo-A, IL-13, and Visfatin to serve as AD- and inflammation-related markers. For detection of kit-binding properties, we checked the expression levels of amyloid beta (A beta), tau protein, and inflammatory mediators in APP/PS/ApoE knockdown (KD) mice and a control group using co-localisation analysis conducted with a confoca I microscope. Using a similar approach, we checked the expression levels of miRNAs in HT22 cells. Finally, we used the plasma from AD patients to confirm that our fluorescent nanoparticles and the WO2002/088706 kit will provide a possible early diagnosis to serve as an AD detector that can be further improved for future studies on targeting AD.
引用
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页数:12
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