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A novel kit for early diagnosis of Alzheimer's disease using a fluorescent nanoparticle imaging.
Park, Jun Sung; Kim, Sang Tae; Kim, Sang Yun; Jo, Min Gi; Choi, Myeong Jun; Kim, Myeong Ok.
Afiliação
  • Park JS; Division of Life Science and Applied Life Science (BK21 plus), College of Natural Sciences, Gyeongsang National University (GNU), Jinju, 52802, Republic of Korea.
  • Kim ST; Department of Neurology, Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, 13605, Republic of Korea.
  • Kim SY; Department of Neurology, Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, 13605, Republic of Korea.
  • Jo MG; Division of Life Science and Applied Life Science (BK21 plus), College of Natural Sciences, Gyeongsang National University (GNU), Jinju, 52802, Republic of Korea.
  • Choi MJ; Research and Development Center, Phytos Inc, Anyang mega valley 609, 268, Anyang, Gyeonggi-do, Republic of Korea.
  • Kim MO; Division of Life Science and Applied Life Science (BK21 plus), College of Natural Sciences, Gyeongsang National University (GNU), Jinju, 52802, Republic of Korea. mokim@gnu.ac.kr.
Sci Rep ; 9(1): 13184, 2019 Sep 12.
Article em En | MEDLINE | ID: mdl-31515517
ABSTRACT
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, Aß1-42 monomer (mAß), Aß1-42 oligomer (oAß), 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 (Aß), tau protein, and inflammatory mediators in APP/PS/ApoE knockdown (KD) mice and a control group using co-localisation analysis conducted with a confocal 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligonucleotídeos / Kit de Reagentes para Diagnóstico / Nanopartículas / Doença de Alzheimer / Imagem Óptica / Corantes Fluorescentes Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligonucleotídeos / Kit de Reagentes para Diagnóstico / Nanopartículas / Doença de Alzheimer / Imagem Óptica / Corantes Fluorescentes Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article