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

被引:28
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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共 53 条
[1]   In Vivo Imaging of CNS Injury and Disease [J].
Akassoglou, Katerina ;
Merlini, Mario ;
Rafalski, Victoria A. ;
Real, Raquel ;
Liang, Liang ;
Jin, Yunju ;
Dougherty, Sarah E. ;
De Paola, Vincenzo ;
Linden, David J. ;
Misgeld, Thomas ;
Zheng, Binhai .
JOURNAL OF NEUROSCIENCE, 2017, 37 (45) :10808-10816
[2]   Inflammation and Alzheimer's disease [J].
Akiyama, H ;
Barger, S ;
Barnum, S ;
Bradt, B ;
Bauer, J ;
Cole, GM ;
Cooper, NR ;
Eikelenboom, P ;
Emmerling, M ;
Fiebich, BL ;
Finch, CE ;
Frautschy, S ;
Griffin, WST ;
Hampel, H ;
Hull, M ;
Landreth, G ;
Lue, LF ;
Mrak, R ;
Mackenzie, IR ;
McGeer, PL ;
O'Banion, MK ;
Pachter, J ;
Pasinetti, G ;
Plata-Salaman, C ;
Rogers, J ;
Rydel, R ;
Shen, Y ;
Streit, W ;
Strohmeyer, R ;
Tooyoma, I ;
Van Muiswinkel, FL ;
Veerhuis, R ;
Walker, D ;
Webster, S ;
Wegrzyniak, B ;
Wenk, G ;
Wyss-Coray, T .
NEUROBIOLOGY OF AGING, 2000, 21 (03) :383-421
[3]  
Alzheimer A, 1995, Clin Anat, V8, P429
[4]   Anthocyanins encapsulated by PLGA@PEG nanoparticles potentially improved its free radical scavenging capabilities via p38/JNK pathway against Aβ1-42-induced oxidative stress [J].
Ul Amin, Faiz ;
Shah, Shahid Ali ;
Badshah, Haroon ;
Khan, Mehtab ;
Kim, Myeong Ok .
JOURNAL OF NANOBIOTECHNOLOGY, 2017, 15
[5]   Therapeutics of Alzheimer's disease: Past, present and future [J].
Anand, R. ;
Gill, Kiran Dip ;
Mahdi, Abbas Ali .
NEUROPHARMACOLOGY, 2014, 76 :27-50
[6]   Current opinion in Alzheimer's disease therapy by nanotechnology-based approaches [J].
Ansari, Shakeel Ahmed ;
Satar, Rukhsana ;
Perveen, Asma ;
Ashraf, Ghulam Md .
CURRENT OPINION IN PSYCHIATRY, 2017, 30 (02) :128-135
[7]   Statins more than cholesterol lowering agents in Alzheimer disease: Their pleiotropic functions as potential therapeutic targets [J].
Barone, Eugenio ;
Di Domenico, Fabio ;
Butterfield, D. Allan .
BIOCHEMICAL PHARMACOLOGY, 2014, 88 (04) :605-616
[8]   A Panel of Serum MiRNA Biomarkers for the Diagnosis of Severe to Mild Traumatic Brain Injury in Humans [J].
Bhomia, Manish ;
Balakathiresan, Nagaraja S. ;
Wang, Kevin K. ;
Papa, Linda ;
Maheshwari, Radha K. .
SCIENTIFIC REPORTS, 2016, 6
[9]   Nanotechnologies for Alzheimer's disease: diagnosis, therapy, and safety issues [J].
Brambilla, Davide ;
Le Droumaguet, Benjamin ;
Nicolas, Julien ;
Hashemi, S. Hossein ;
Wu, Lin-Ping ;
Moghimi, S. Moein ;
Couvreur, Patrick ;
Andrieux, Karine .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2011, 7 (05) :521-540
[10]   The road to restoring neural circuits for the treatment of Alzheimer's disease [J].
Canter, Rebecca G. ;
Penney, Jay ;
Tsai, Li-Huei .
NATURE, 2016, 539 (7628) :187-196