S100A11 (calgizzarin) is released via NETosis in rheumatoid arthritis (RA) and stimulates IL-6 and TNF secretion by neutrophils

Abstract S100A11 (calgizzarin), a member of S100 family, is associated with several autoimmune diseases, including rheumatoid arthritis (RA). Neutrophil extracellular traps (NETs) are implicated in the pathogenesis of RA and in the externalization of some S100 family members. Therefore, we aimed to...

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Autores principales: Adéla Navrátilová, Viktor Bečvář, Jiří Baloun, Dres Damgaard, Claus Henrik Nielsen, David Veigl, Karel Pavelka, Jiří Vencovský, Ladislav Šenolt, Lucie Andrés Cerezo
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:c104c105a63f43e199fcdc8d9122af452021-12-02T16:31:02ZS100A11 (calgizzarin) is released via NETosis in rheumatoid arthritis (RA) and stimulates IL-6 and TNF secretion by neutrophils10.1038/s41598-021-85561-32045-2322https://doaj.org/article/c104c105a63f43e199fcdc8d9122af452021-03-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-85561-3https://doaj.org/toc/2045-2322Abstract S100A11 (calgizzarin), a member of S100 family, is associated with several autoimmune diseases, including rheumatoid arthritis (RA). Neutrophil extracellular traps (NETs) are implicated in the pathogenesis of RA and in the externalization of some S100 family members. Therefore, we aimed to determine the association between S100A11 and NETs in RA. For this purpose, the levels of S100A11 and NETosis markers were detected in the RA synovial fluid by immunoassays. The expression of S100A11 by neutrophils in the RA synovial tissue was assessed. Neutrophils isolated from peripheral blood were exposed to S100A11 or stimulated to release NETs. The levels of NETosis- and inflammation-associated proteins were analysed by immunoassays. NETs were visualized by immunofluorescence. We showed that S100A11 was expressed by the neutrophils in the RA synovial tissue. Moreover, S100A11 in the RA synovial fluid correlated with several NETosis markers. In vitro, S100A11 was abundantly released by neutrophils undergoing NETosis compared to untreated cells (p < 0.001). Extracellular S100A11 increased the secretion of IL-6 (p < 0.05) and TNF (p < 0.05) by neutrophils but did not induce NETosis. This study demonstrates, for the first time, that the release of S100A11 is dependent on NETosis and that extracellular S100A11 augments the inflammatory response by inducing pro-inflammatory cytokines in neutrophils.Adéla NavrátilováViktor BečvářJiří BalounDres DamgaardClaus Henrik NielsenDavid VeiglKarel PavelkaJiří VencovskýLadislav ŠenoltLucie Andrés CerezoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Adéla Navrátilová
Viktor Bečvář
Jiří Baloun
Dres Damgaard
Claus Henrik Nielsen
David Veigl
Karel Pavelka
Jiří Vencovský
Ladislav Šenolt
Lucie Andrés Cerezo
S100A11 (calgizzarin) is released via NETosis in rheumatoid arthritis (RA) and stimulates IL-6 and TNF secretion by neutrophils
description Abstract S100A11 (calgizzarin), a member of S100 family, is associated with several autoimmune diseases, including rheumatoid arthritis (RA). Neutrophil extracellular traps (NETs) are implicated in the pathogenesis of RA and in the externalization of some S100 family members. Therefore, we aimed to determine the association between S100A11 and NETs in RA. For this purpose, the levels of S100A11 and NETosis markers were detected in the RA synovial fluid by immunoassays. The expression of S100A11 by neutrophils in the RA synovial tissue was assessed. Neutrophils isolated from peripheral blood were exposed to S100A11 or stimulated to release NETs. The levels of NETosis- and inflammation-associated proteins were analysed by immunoassays. NETs were visualized by immunofluorescence. We showed that S100A11 was expressed by the neutrophils in the RA synovial tissue. Moreover, S100A11 in the RA synovial fluid correlated with several NETosis markers. In vitro, S100A11 was abundantly released by neutrophils undergoing NETosis compared to untreated cells (p < 0.001). Extracellular S100A11 increased the secretion of IL-6 (p < 0.05) and TNF (p < 0.05) by neutrophils but did not induce NETosis. This study demonstrates, for the first time, that the release of S100A11 is dependent on NETosis and that extracellular S100A11 augments the inflammatory response by inducing pro-inflammatory cytokines in neutrophils.
format article
author Adéla Navrátilová
Viktor Bečvář
Jiří Baloun
Dres Damgaard
Claus Henrik Nielsen
David Veigl
Karel Pavelka
Jiří Vencovský
Ladislav Šenolt
Lucie Andrés Cerezo
author_facet Adéla Navrátilová
Viktor Bečvář
Jiří Baloun
Dres Damgaard
Claus Henrik Nielsen
David Veigl
Karel Pavelka
Jiří Vencovský
Ladislav Šenolt
Lucie Andrés Cerezo
author_sort Adéla Navrátilová
title S100A11 (calgizzarin) is released via NETosis in rheumatoid arthritis (RA) and stimulates IL-6 and TNF secretion by neutrophils
title_short S100A11 (calgizzarin) is released via NETosis in rheumatoid arthritis (RA) and stimulates IL-6 and TNF secretion by neutrophils
title_full S100A11 (calgizzarin) is released via NETosis in rheumatoid arthritis (RA) and stimulates IL-6 and TNF secretion by neutrophils
title_fullStr S100A11 (calgizzarin) is released via NETosis in rheumatoid arthritis (RA) and stimulates IL-6 and TNF secretion by neutrophils
title_full_unstemmed S100A11 (calgizzarin) is released via NETosis in rheumatoid arthritis (RA) and stimulates IL-6 and TNF secretion by neutrophils
title_sort s100a11 (calgizzarin) is released via netosis in rheumatoid arthritis (ra) and stimulates il-6 and tnf secretion by neutrophils
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/c104c105a63f43e199fcdc8d9122af45
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