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Association between CCR2 and CCL2 expression and NET stimulation in adult-onset Still’s disease
Adult-onset Still’s disease (AOSD) is a systemic inflammatory disease characterized by the activation of monocyte-derived cells and the release of neutrophil extracellular traps (NET). C–C motif ligand (CCL) 2 is a chemoattractant that interacts with the C–C motif chemokine receptor (CCR) 2, resulti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374521/ https://www.ncbi.nlm.nih.gov/pubmed/37500699 http://dx.doi.org/10.1038/s41598-023-39517-4 |
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author | Jung, Ju-Yang Ahn, Mi-Hyun Kim, Ji-Won Suh, Chang-Hee Han, Jae Ho Kim, Hyoun-Ah |
author_facet | Jung, Ju-Yang Ahn, Mi-Hyun Kim, Ji-Won Suh, Chang-Hee Han, Jae Ho Kim, Hyoun-Ah |
author_sort | Jung, Ju-Yang |
collection | PubMed |
description | Adult-onset Still’s disease (AOSD) is a systemic inflammatory disease characterized by the activation of monocyte-derived cells and the release of neutrophil extracellular traps (NET). C–C motif ligand (CCL) 2 is a chemoattractant that interacts with the C–C motif chemokine receptor (CCR) 2, resulting in monocyte recruitment and activation. CCL2 and CCR2 were measured with enzyme-linked immunosorbent assay (ELISA) at the serum level, and using immunohistochemical staining at the skin and lymph node tissues levels. THP-1 cell lysates were analyzed using western blot and ELISA after NET stimulation in patients with AOSD. Serum CCL2 level was higher in patients with AOSD than in patients with rheumatoid arthritis and healthy controls (HCs). In patients with AOSD, the percentage of CCL2-positive inflammatory cells in the skin tissues and CCR2-positive inflammatory cells in the lymph nodes increased, compared to that in HCs and in patients with reactive lymphadenopathy, respectively. NET induced in patients with AOSD enhanced the secretion of CCR2, higher CCR2 expression in monocytes, and the levels of interleukin (IL)-1β, IL-6, and IL-18 from THP-1 cells. Our findings suggest that upregulation of the CCL2–CCR2 axis may contribute to the clinical and inflammatory characteristics of AOSD. |
format | Online Article Text |
id | pubmed-10374521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103745212023-07-29 Association between CCR2 and CCL2 expression and NET stimulation in adult-onset Still’s disease Jung, Ju-Yang Ahn, Mi-Hyun Kim, Ji-Won Suh, Chang-Hee Han, Jae Ho Kim, Hyoun-Ah Sci Rep Article Adult-onset Still’s disease (AOSD) is a systemic inflammatory disease characterized by the activation of monocyte-derived cells and the release of neutrophil extracellular traps (NET). C–C motif ligand (CCL) 2 is a chemoattractant that interacts with the C–C motif chemokine receptor (CCR) 2, resulting in monocyte recruitment and activation. CCL2 and CCR2 were measured with enzyme-linked immunosorbent assay (ELISA) at the serum level, and using immunohistochemical staining at the skin and lymph node tissues levels. THP-1 cell lysates were analyzed using western blot and ELISA after NET stimulation in patients with AOSD. Serum CCL2 level was higher in patients with AOSD than in patients with rheumatoid arthritis and healthy controls (HCs). In patients with AOSD, the percentage of CCL2-positive inflammatory cells in the skin tissues and CCR2-positive inflammatory cells in the lymph nodes increased, compared to that in HCs and in patients with reactive lymphadenopathy, respectively. NET induced in patients with AOSD enhanced the secretion of CCR2, higher CCR2 expression in monocytes, and the levels of interleukin (IL)-1β, IL-6, and IL-18 from THP-1 cells. Our findings suggest that upregulation of the CCL2–CCR2 axis may contribute to the clinical and inflammatory characteristics of AOSD. Nature Publishing Group UK 2023-07-27 /pmc/articles/PMC10374521/ /pubmed/37500699 http://dx.doi.org/10.1038/s41598-023-39517-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jung, Ju-Yang Ahn, Mi-Hyun Kim, Ji-Won Suh, Chang-Hee Han, Jae Ho Kim, Hyoun-Ah Association between CCR2 and CCL2 expression and NET stimulation in adult-onset Still’s disease |
title | Association between CCR2 and CCL2 expression and NET stimulation in adult-onset Still’s disease |
title_full | Association between CCR2 and CCL2 expression and NET stimulation in adult-onset Still’s disease |
title_fullStr | Association between CCR2 and CCL2 expression and NET stimulation in adult-onset Still’s disease |
title_full_unstemmed | Association between CCR2 and CCL2 expression and NET stimulation in adult-onset Still’s disease |
title_short | Association between CCR2 and CCL2 expression and NET stimulation in adult-onset Still’s disease |
title_sort | association between ccr2 and ccl2 expression and net stimulation in adult-onset still’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374521/ https://www.ncbi.nlm.nih.gov/pubmed/37500699 http://dx.doi.org/10.1038/s41598-023-39517-4 |
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