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Detection and Assessment of α-Synuclein Oligomers in the Urine of Parkinson's Disease Patients.
Nam, Daleum; Lee, Jee-Young; Lee, Minhyung; Kim, Janghwan; Seol, Wongi; Son, Ilhong; Ho, Dong Hwan.
Afiliación
  • Nam D; InAm Neuroscience Research Center, Sanbon Medical Center, College of Medicine, Wonkwang University, Gunposi, Gyeonggido, Republic of Korea.
  • Lee JY; Department of Neurology, Seoul National University Boramae Medical Center, Seoul, Republic of Korea.
  • Lee M; Stem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
  • Kim J; Department of Functional Genomics, KRIBB School of Bioscience, University of Science and Technology, Daejeon, Republic of Korea.
  • Seol W; Stem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.
  • Son I; Department of Functional Genomics, KRIBB School of Bioscience, University of Science and Technology, Daejeon, Republic of Korea.
  • Ho DH; InAm Neuroscience Research Center, Sanbon Medical Center, College of Medicine, Wonkwang University, Gunposi, Gyeonggido, Republic of Korea.
J Parkinsons Dis ; 10(3): 981-991, 2020.
Article en En | MEDLINE | ID: mdl-32444560
ABSTRACT

BACKGROUND:

α-Synuclein (α-syn) is a major component of Lewy bodies, a pathologic marker of Parkinson's disease (PD) in post-mortem studies. The use of α-syn as a practical PD biomarker has been investigated by numerous researchers. However, reports of differences in α-syn levels in biofluids, such as cerebrospinal fluid, plasma, and saliva, between PD patients and controls are inconsistent. Recently, the measurement of α-syn oligomer levels has emerged as a novel approach to diagnose PD.

OBJECTIVE:

Lysates and culture media from two different types of dopaminergic neuronal cells or urine samples from 11 non-PD and 21 PD patients were collected and analyzed.

METHODS:

We developed and performed an enzyme-linked immuno-absorbent assay (ELISA) to detect various oligomeric α-syn using distinct pairs of antibodies.

RESULTS:

We validated our ELISA using rotenone-induced alterations of α-syn levels in human dopaminergic neurons. Total urinary α-syn levels, measured using our ELISA method, showed no difference between PD and non-PD individuals, but a higher level of α-syn oligomer recognized by MJFR-14-6-5-2 in PD urine samples was observed. Levels of distinct oligomeric α-syn detected by ASyO5 were lower in PD urine samples. Three different α-syn ELISA results were analyzed with respect to the severity of PD, but only the correlation between total α-syn levels and PD index was significant.

CONCLUSION:

Our findings suggest that detection of distinct oligomeric formations of α-syn and measurement of their levels in urine might be feasible for use in PD diagnostics.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Biomarcadores / Alfa-Sinucleína Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: J Parkinsons Dis Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Biomarcadores / Alfa-Sinucleína Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: J Parkinsons Dis Año: 2020 Tipo del documento: Article