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Elevated macrophage-inducible C-type lectin expression in the synovial tissue of patients with rheumatoid arthritis

Rheumatoid arthritis (RA), a systemic autoimmune disease, is known to cause chronic inflammation in synovial joints. A number of inflammatory conditions are associated with stimulation of Clec4e, a macrophage-inducible C-type lectin (MINCLE) and transmembrane pattern recognition receptor that functi...

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Autores principales: Takata, Ken, Takano, Shotaro, Miyagi, Masayuki, Mukai, Manabu, Iwase, Dai, Aikawa, Jun, Ohashi, Yoshihisa, Inoue, Gen, Takaso, Masashi, Uchida, Kentaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8808308/
https://www.ncbi.nlm.nih.gov/pubmed/35125945
http://dx.doi.org/10.5114/ceji.2021.111471
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author Takata, Ken
Takano, Shotaro
Miyagi, Masayuki
Mukai, Manabu
Iwase, Dai
Aikawa, Jun
Ohashi, Yoshihisa
Inoue, Gen
Takaso, Masashi
Uchida, Kentaro
author_facet Takata, Ken
Takano, Shotaro
Miyagi, Masayuki
Mukai, Manabu
Iwase, Dai
Aikawa, Jun
Ohashi, Yoshihisa
Inoue, Gen
Takaso, Masashi
Uchida, Kentaro
author_sort Takata, Ken
collection PubMed
description Rheumatoid arthritis (RA), a systemic autoimmune disease, is known to cause chronic inflammation in synovial joints. A number of inflammatory conditions are associated with stimulation of Clec4e, a macrophage-inducible C-type lectin (MINCLE) and transmembrane pattern recognition receptor that functions in innate immunity. We previously reported MINCLE expression in synovial macrophages isolated from the synovium of osteoarthritis (OA) patients. However, MINCLE expression has not been examined in RA synovial tissue. To examine MINCLE expression in RA patients, synovial tissue specimens were obtained from patients with RA and OA during joint replacement surgery (n = 20 each). Total RNA was extracted from synovial tissue and used to compare MINCLE expression in OA and RA (n = 15 each). We also extracted fresh CD14+ (macrophage-rich) and CD14– cell fractions from synovial tissue and compared MINCLE expression between OA and RA patients (n = 5 each). MINCLE levels in synovial tissue were significantly elevated in RA patients compared to OA patients. MINCLE expression was significantly elevated in the CD14+ fraction compared to the CD14– fraction in both OA and RA patients. Further, while there were no differences in the CD14+ fraction between RA and OA, MINCLE expression in the CD14– fraction was elevated in RA compared to OA. Our findings indicate that MINCLE expression is elevated in the synovium of RA patients and that MINCLE expression in non-macrophage cell fractions may be a key feature of RA.
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spelling pubmed-88083082022-02-04 Elevated macrophage-inducible C-type lectin expression in the synovial tissue of patients with rheumatoid arthritis Takata, Ken Takano, Shotaro Miyagi, Masayuki Mukai, Manabu Iwase, Dai Aikawa, Jun Ohashi, Yoshihisa Inoue, Gen Takaso, Masashi Uchida, Kentaro Cent Eur J Immunol Clinical Immunology Rheumatoid arthritis (RA), a systemic autoimmune disease, is known to cause chronic inflammation in synovial joints. A number of inflammatory conditions are associated with stimulation of Clec4e, a macrophage-inducible C-type lectin (MINCLE) and transmembrane pattern recognition receptor that functions in innate immunity. We previously reported MINCLE expression in synovial macrophages isolated from the synovium of osteoarthritis (OA) patients. However, MINCLE expression has not been examined in RA synovial tissue. To examine MINCLE expression in RA patients, synovial tissue specimens were obtained from patients with RA and OA during joint replacement surgery (n = 20 each). Total RNA was extracted from synovial tissue and used to compare MINCLE expression in OA and RA (n = 15 each). We also extracted fresh CD14+ (macrophage-rich) and CD14– cell fractions from synovial tissue and compared MINCLE expression between OA and RA patients (n = 5 each). MINCLE levels in synovial tissue were significantly elevated in RA patients compared to OA patients. MINCLE expression was significantly elevated in the CD14+ fraction compared to the CD14– fraction in both OA and RA patients. Further, while there were no differences in the CD14+ fraction between RA and OA, MINCLE expression in the CD14– fraction was elevated in RA compared to OA. Our findings indicate that MINCLE expression is elevated in the synovium of RA patients and that MINCLE expression in non-macrophage cell fractions may be a key feature of RA. Termedia Publishing House 2021-12-03 2021 /pmc/articles/PMC8808308/ /pubmed/35125945 http://dx.doi.org/10.5114/ceji.2021.111471 Text en Copyright © 2021 Termedia https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/) )
spellingShingle Clinical Immunology
Takata, Ken
Takano, Shotaro
Miyagi, Masayuki
Mukai, Manabu
Iwase, Dai
Aikawa, Jun
Ohashi, Yoshihisa
Inoue, Gen
Takaso, Masashi
Uchida, Kentaro
Elevated macrophage-inducible C-type lectin expression in the synovial tissue of patients with rheumatoid arthritis
title Elevated macrophage-inducible C-type lectin expression in the synovial tissue of patients with rheumatoid arthritis
title_full Elevated macrophage-inducible C-type lectin expression in the synovial tissue of patients with rheumatoid arthritis
title_fullStr Elevated macrophage-inducible C-type lectin expression in the synovial tissue of patients with rheumatoid arthritis
title_full_unstemmed Elevated macrophage-inducible C-type lectin expression in the synovial tissue of patients with rheumatoid arthritis
title_short Elevated macrophage-inducible C-type lectin expression in the synovial tissue of patients with rheumatoid arthritis
title_sort elevated macrophage-inducible c-type lectin expression in the synovial tissue of patients with rheumatoid arthritis
topic Clinical Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8808308/
https://www.ncbi.nlm.nih.gov/pubmed/35125945
http://dx.doi.org/10.5114/ceji.2021.111471
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