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A proteomic analysis of serum-derived exosomes in rheumatoid arthritis

BACKGROUND: To understand the roles of serum exosomes in rheumatoid arthritis (RA), we comprehensively investigated the protein profiles of serum exosomes in patients with RA. METHODS: Exosomes were isolated from serum samples obtained from 33 patients (12 with active RA [aRA], 11 with inactive RA [...

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Autores principales: Tsuno, Hirotaka, Arito, Mitsumi, Suematsu, Naoya, Sato, Toshiyuki, Hashimoto, Atsushi, Matsui, Toshihiro, Omoteyama, Kazuki, Sato, Masaaki, Okamoto, Kazuki, Tohma, Shigeto, Kurokawa, Manae S., Kato, Tomohiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390805/
https://www.ncbi.nlm.nih.gov/pubmed/30886985
http://dx.doi.org/10.1186/s41927-018-0041-8
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author Tsuno, Hirotaka
Arito, Mitsumi
Suematsu, Naoya
Sato, Toshiyuki
Hashimoto, Atsushi
Matsui, Toshihiro
Omoteyama, Kazuki
Sato, Masaaki
Okamoto, Kazuki
Tohma, Shigeto
Kurokawa, Manae S.
Kato, Tomohiro
author_facet Tsuno, Hirotaka
Arito, Mitsumi
Suematsu, Naoya
Sato, Toshiyuki
Hashimoto, Atsushi
Matsui, Toshihiro
Omoteyama, Kazuki
Sato, Masaaki
Okamoto, Kazuki
Tohma, Shigeto
Kurokawa, Manae S.
Kato, Tomohiro
author_sort Tsuno, Hirotaka
collection PubMed
description BACKGROUND: To understand the roles of serum exosomes in rheumatoid arthritis (RA), we comprehensively investigated the protein profiles of serum exosomes in patients with RA. METHODS: Exosomes were isolated from serum samples obtained from 33 patients (12 with active RA [aRA], 11 with inactive RA [iRA], 10 with osteoarthritis [OA]) and 10 healthy donors (HLs). Proteins extracted from the exosomes were separated by two-dimensional differential gel electrophoresis (2D-DIGE) and identified by mass spectrometry. RESULTS: In total, 204 protein spots were detected by 2D-DIGE. In the aRA, iRA, and OA groups, 24, 5, and 7 spots showed approximately ≥ ±1.3-fold intensity differences compared with the HL group, respectively. We were able to identify proteins in six protein spots. Among them, the protein spot identified as Toll-like receptor 3 (TLR3) showed approximately 6-fold higher intensity in the aRA group than in the other groups. CONCLUSIONS: Patients with active RA possessed considerably different protein profiles of serum exosomes from patients with iRA, patients with OA, and healthy donors. The unique protein profile of serum exosomes, such as the possession of abundant TLR3 fragments, may reflect the pathophysiology of active RA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s41927-018-0041-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-63908052019-03-18 A proteomic analysis of serum-derived exosomes in rheumatoid arthritis Tsuno, Hirotaka Arito, Mitsumi Suematsu, Naoya Sato, Toshiyuki Hashimoto, Atsushi Matsui, Toshihiro Omoteyama, Kazuki Sato, Masaaki Okamoto, Kazuki Tohma, Shigeto Kurokawa, Manae S. Kato, Tomohiro BMC Rheumatol Research Article BACKGROUND: To understand the roles of serum exosomes in rheumatoid arthritis (RA), we comprehensively investigated the protein profiles of serum exosomes in patients with RA. METHODS: Exosomes were isolated from serum samples obtained from 33 patients (12 with active RA [aRA], 11 with inactive RA [iRA], 10 with osteoarthritis [OA]) and 10 healthy donors (HLs). Proteins extracted from the exosomes were separated by two-dimensional differential gel electrophoresis (2D-DIGE) and identified by mass spectrometry. RESULTS: In total, 204 protein spots were detected by 2D-DIGE. In the aRA, iRA, and OA groups, 24, 5, and 7 spots showed approximately ≥ ±1.3-fold intensity differences compared with the HL group, respectively. We were able to identify proteins in six protein spots. Among them, the protein spot identified as Toll-like receptor 3 (TLR3) showed approximately 6-fold higher intensity in the aRA group than in the other groups. CONCLUSIONS: Patients with active RA possessed considerably different protein profiles of serum exosomes from patients with iRA, patients with OA, and healthy donors. The unique protein profile of serum exosomes, such as the possession of abundant TLR3 fragments, may reflect the pathophysiology of active RA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s41927-018-0041-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-27 /pmc/articles/PMC6390805/ /pubmed/30886985 http://dx.doi.org/10.1186/s41927-018-0041-8 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Tsuno, Hirotaka
Arito, Mitsumi
Suematsu, Naoya
Sato, Toshiyuki
Hashimoto, Atsushi
Matsui, Toshihiro
Omoteyama, Kazuki
Sato, Masaaki
Okamoto, Kazuki
Tohma, Shigeto
Kurokawa, Manae S.
Kato, Tomohiro
A proteomic analysis of serum-derived exosomes in rheumatoid arthritis
title A proteomic analysis of serum-derived exosomes in rheumatoid arthritis
title_full A proteomic analysis of serum-derived exosomes in rheumatoid arthritis
title_fullStr A proteomic analysis of serum-derived exosomes in rheumatoid arthritis
title_full_unstemmed A proteomic analysis of serum-derived exosomes in rheumatoid arthritis
title_short A proteomic analysis of serum-derived exosomes in rheumatoid arthritis
title_sort proteomic analysis of serum-derived exosomes in rheumatoid arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390805/
https://www.ncbi.nlm.nih.gov/pubmed/30886985
http://dx.doi.org/10.1186/s41927-018-0041-8
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