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Differential effects of interleukin-17A and 17F on cell interactions between immune cells and stromal cells from synovium or skin

We compared the contribution of IL-17A and IL-17F in co-culture systems mimicking cell interactions as found in inflamed synovium and skin. Synoviocytes or skin fibroblasts were co-cultured with activated PBMC, with IL-17A, IL-17 A/F, IL-17F, IL-23, anti-IL-17A, anti-IL-17A/F or anti-IL-17F antibodi...

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Autores principales: Tout, Issam, Noack, Mélissa, Miossec, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628108/
https://www.ncbi.nlm.nih.gov/pubmed/37932356
http://dx.doi.org/10.1038/s41598-023-45653-8
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author Tout, Issam
Noack, Mélissa
Miossec, Pierre
author_facet Tout, Issam
Noack, Mélissa
Miossec, Pierre
author_sort Tout, Issam
collection PubMed
description We compared the contribution of IL-17A and IL-17F in co-culture systems mimicking cell interactions as found in inflamed synovium and skin. Synoviocytes or skin fibroblasts were co-cultured with activated PBMC, with IL-17A, IL-17 A/F, IL-17F, IL-23, anti-IL-17A, anti-IL-17A/F or anti-IL-17F antibodies. IL-17A, IL-17F, IL-6 and IL-10 production was measured at 48 h. mRNA expression of receptor subunits for IL-23, IL-12 and IL-17 was assessed at 24 h. Both cell activation and interactions were needed for a high IL-17A secretion while IL-17F was stimulated by PHA activation alone and further increased in co-cultures. IL-17F levels were higher than IL-17A in both co-cultures (p < 0.05). IL-17F addition decreased IL-17A secretion (p < 0.05) but IL-17A addition had no effect on IL-17F secretion. Interestingly, IL-17A and IL-17F upregulated IL-17RA and IL-17RC mRNA expression in PBMC/skin fibroblast co-cultures (p < 0.05) while only IL-17F exerted this effect in synoviocytes (p < 0.05). Monocyte exclusion in both co-cultures increased IL-17A and IL-17F (twofold, p < 0.05) while decreasing IL-10 and IL-6 secretion (twofold, p < 0.05). IL-17A and F had differential effects on their receptor expression with a higher sensitivity for skin fibroblasts highlighting the differential contribution of IL-17A and F in joint vs. skin diseases.
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spelling pubmed-106281082023-11-08 Differential effects of interleukin-17A and 17F on cell interactions between immune cells and stromal cells from synovium or skin Tout, Issam Noack, Mélissa Miossec, Pierre Sci Rep Article We compared the contribution of IL-17A and IL-17F in co-culture systems mimicking cell interactions as found in inflamed synovium and skin. Synoviocytes or skin fibroblasts were co-cultured with activated PBMC, with IL-17A, IL-17 A/F, IL-17F, IL-23, anti-IL-17A, anti-IL-17A/F or anti-IL-17F antibodies. IL-17A, IL-17F, IL-6 and IL-10 production was measured at 48 h. mRNA expression of receptor subunits for IL-23, IL-12 and IL-17 was assessed at 24 h. Both cell activation and interactions were needed for a high IL-17A secretion while IL-17F was stimulated by PHA activation alone and further increased in co-cultures. IL-17F levels were higher than IL-17A in both co-cultures (p < 0.05). IL-17F addition decreased IL-17A secretion (p < 0.05) but IL-17A addition had no effect on IL-17F secretion. Interestingly, IL-17A and IL-17F upregulated IL-17RA and IL-17RC mRNA expression in PBMC/skin fibroblast co-cultures (p < 0.05) while only IL-17F exerted this effect in synoviocytes (p < 0.05). Monocyte exclusion in both co-cultures increased IL-17A and IL-17F (twofold, p < 0.05) while decreasing IL-10 and IL-6 secretion (twofold, p < 0.05). IL-17A and F had differential effects on their receptor expression with a higher sensitivity for skin fibroblasts highlighting the differential contribution of IL-17A and F in joint vs. skin diseases. Nature Publishing Group UK 2023-11-06 /pmc/articles/PMC10628108/ /pubmed/37932356 http://dx.doi.org/10.1038/s41598-023-45653-8 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
Tout, Issam
Noack, Mélissa
Miossec, Pierre
Differential effects of interleukin-17A and 17F on cell interactions between immune cells and stromal cells from synovium or skin
title Differential effects of interleukin-17A and 17F on cell interactions between immune cells and stromal cells from synovium or skin
title_full Differential effects of interleukin-17A and 17F on cell interactions between immune cells and stromal cells from synovium or skin
title_fullStr Differential effects of interleukin-17A and 17F on cell interactions between immune cells and stromal cells from synovium or skin
title_full_unstemmed Differential effects of interleukin-17A and 17F on cell interactions between immune cells and stromal cells from synovium or skin
title_short Differential effects of interleukin-17A and 17F on cell interactions between immune cells and stromal cells from synovium or skin
title_sort differential effects of interleukin-17a and 17f on cell interactions between immune cells and stromal cells from synovium or skin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628108/
https://www.ncbi.nlm.nih.gov/pubmed/37932356
http://dx.doi.org/10.1038/s41598-023-45653-8
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