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Open AccessCommunication
Int. J. Mol. Sci. 2016, 17(10), 1634; doi:10.3390/ijms17101634

Disruption of Membranes of Extracellular Vesicles Is Necessary for ELISA Determination of Urine AQP2: Proof of Disruption and Epitopes of AQP2 Antibodies

1
Electron Microscope Core Facility, Niigata University, Niigata 951-851, Japan
2
Department of Research and Development, Diagnostic Division, Otsuka Pharmaceutical Co., Ltd., Tokusima 771-0182, Japan
3
Department of Medical Innovations, New Drug Research Division, Otsuka Pharmaceutical Co., Ltd., Tokusima 771-0192, Japan
4
Biofluid Biomarker Center, Institute of Social Innovation and Promotion, Niigata University, Niigata 950-2181, Japan
5
Department of Pathophysiology, Meiji Pharmaceutical University, Tokyo 204-8588, Japan
6
Department of Nephrology, Tokyo Medical and Dental University, Tokyo 113-8519, Japan
*
Author to whom correspondence should be addressed.
Academic Editor: Gregor Drummen
Received: 30 May 2016 / Revised: 15 September 2016 / Accepted: 19 September 2016 / Published: 26 September 2016
(This article belongs to the Special Issue Aquaporin)
View Full-Text   |   Download PDF [11478 KB, uploaded 26 September 2016]   |  

Abstract

Aquaporin-2 (AQP2) is present in urine extracellular vesicles (EVs) and is a useful biomarker for water balance disorders. We previously found that pre-treatment of urine with alkali/detergent or storage at −25 °C is required for enzyme-linked immunosorbent assay (ELISA) measurement. We speculated that disruptions of EVs membranes are necessary to allow for the direct contact of antibodies with their epitopes. Human urine EVs were prepared using an ultracentrifugation method. Urine EV samples were stored at different temperatures for a week. Electron microscopy showed abundant EVs with diameters of 20–100 nm, consistent with those of exosomes, in normal urine, whereas samples from alkali/detergent pre-treated urine showed fewer EVs with large swollen shapes and frequent membrane disruptions. The abundance and structures of EVs were maintained during storage at −80 °C, but were severely damaged at −25 °C. Binding and competitive inhibition assays showed that epitopes of monoclonal antibody and polyclonal antibody were the hydrophilic Loop D and C-terminus of AQP2, respectively, both of which are present on the inner surface of EVs. Thus, urine storage at −25 °C or pre-treatment with alkali/detergent disrupt EVs membranes and allow AQP2 antibodies to bind to their epitopes located inside EVs. View Full-Text
Keywords: aquaporin-2 (AQP2); exosome; extracellular vesicle; ELISA; biomarker; kidney; water-balance aquaporin-2 (AQP2); exosome; extracellular vesicle; ELISA; biomarker; kidney; water-balance
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MDPI and ACS Style

Nameta, M.; Saijo, Y.; Ohmoto, Y.; Katsuragi, K.; Yamamoto, K.; Yamamoto, T.; Ishibashi, K.; Sasaki, S. Disruption of Membranes of Extracellular Vesicles Is Necessary for ELISA Determination of Urine AQP2: Proof of Disruption and Epitopes of AQP2 Antibodies. Int. J. Mol. Sci. 2016, 17, 1634.

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