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Role of the NLRP3 inflammasome in the transient release of IL-1β induced by monosodium urate crystals in human fibroblast-like synoviocytes

BACKGROUND: To investigate whether monosodium urate (MSU) crystals induce interleukin (IL)-1β in human fibroblast-like synoviocytes (FLS), and whether the NLRP3 inflammasome is involved in the inflammatory mechanism. METHODS: Human FLS isolated from explants of synovial tissue were stimulated with M...

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Autores principales: Zheng, Shu-cong, Zhu, Xiao-xia, Xue, Yu, Zhang, Li-hong, Zou, He-jian, Qiu, Jian-hua, Liu, Qiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403983/
https://www.ncbi.nlm.nih.gov/pubmed/25897296
http://dx.doi.org/10.1186/s12950-015-0070-7
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author Zheng, Shu-cong
Zhu, Xiao-xia
Xue, Yu
Zhang, Li-hong
Zou, He-jian
Qiu, Jian-hua
Liu, Qiong
author_facet Zheng, Shu-cong
Zhu, Xiao-xia
Xue, Yu
Zhang, Li-hong
Zou, He-jian
Qiu, Jian-hua
Liu, Qiong
author_sort Zheng, Shu-cong
collection PubMed
description BACKGROUND: To investigate whether monosodium urate (MSU) crystals induce interleukin (IL)-1β in human fibroblast-like synoviocytes (FLS), and whether the NLRP3 inflammasome is involved in the inflammatory mechanism. METHODS: Human FLS isolated from explants of synovial tissue were stimulated with MSU crystals (0.001 to 0.5 mg/ml) for different time course (6 hours to 48 hours). The expressions of IL-1β, IL-6, TNF-α and NLRP3 were evaluated with ELISA, Western blot and quantitative real-time PCR. RESULTS: Exposure of FLS to MSU crystals transiently induced a significant increase in IL-1β expression in culture medium with a peak at 6 h. The mRNA level of IL-1β in the FLS cells had a similar pattern at this time point. Changes in IL-6 and TNF-α expression were not observed. Simultaneously, intercellular pro-IL-1β was detected at 6 h. Furthermore, MSU crystals also induced NLRP3 mRNA and protein expression at 6 h to 48 h after MSU treatment. CONCLUSIONS: MSU crystals directly increased IL-1β and intercellular NLRP3 expression in FLS cells. It is suggested that the NLRP3 inflammasome may be associated with IL-1β in FLS treated with MSU. Altogether, MSU could induce production and release of IL-1β through the NLRP3 inflammasome in human synoviocytes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12950-015-0070-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-44039832015-04-21 Role of the NLRP3 inflammasome in the transient release of IL-1β induced by monosodium urate crystals in human fibroblast-like synoviocytes Zheng, Shu-cong Zhu, Xiao-xia Xue, Yu Zhang, Li-hong Zou, He-jian Qiu, Jian-hua Liu, Qiong J Inflamm (Lond) Research BACKGROUND: To investigate whether monosodium urate (MSU) crystals induce interleukin (IL)-1β in human fibroblast-like synoviocytes (FLS), and whether the NLRP3 inflammasome is involved in the inflammatory mechanism. METHODS: Human FLS isolated from explants of synovial tissue were stimulated with MSU crystals (0.001 to 0.5 mg/ml) for different time course (6 hours to 48 hours). The expressions of IL-1β, IL-6, TNF-α and NLRP3 were evaluated with ELISA, Western blot and quantitative real-time PCR. RESULTS: Exposure of FLS to MSU crystals transiently induced a significant increase in IL-1β expression in culture medium with a peak at 6 h. The mRNA level of IL-1β in the FLS cells had a similar pattern at this time point. Changes in IL-6 and TNF-α expression were not observed. Simultaneously, intercellular pro-IL-1β was detected at 6 h. Furthermore, MSU crystals also induced NLRP3 mRNA and protein expression at 6 h to 48 h after MSU treatment. CONCLUSIONS: MSU crystals directly increased IL-1β and intercellular NLRP3 expression in FLS cells. It is suggested that the NLRP3 inflammasome may be associated with IL-1β in FLS treated with MSU. Altogether, MSU could induce production and release of IL-1β through the NLRP3 inflammasome in human synoviocytes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12950-015-0070-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-10 /pmc/articles/PMC4403983/ /pubmed/25897296 http://dx.doi.org/10.1186/s12950-015-0070-7 Text en © Zheng et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Zheng, Shu-cong
Zhu, Xiao-xia
Xue, Yu
Zhang, Li-hong
Zou, He-jian
Qiu, Jian-hua
Liu, Qiong
Role of the NLRP3 inflammasome in the transient release of IL-1β induced by monosodium urate crystals in human fibroblast-like synoviocytes
title Role of the NLRP3 inflammasome in the transient release of IL-1β induced by monosodium urate crystals in human fibroblast-like synoviocytes
title_full Role of the NLRP3 inflammasome in the transient release of IL-1β induced by monosodium urate crystals in human fibroblast-like synoviocytes
title_fullStr Role of the NLRP3 inflammasome in the transient release of IL-1β induced by monosodium urate crystals in human fibroblast-like synoviocytes
title_full_unstemmed Role of the NLRP3 inflammasome in the transient release of IL-1β induced by monosodium urate crystals in human fibroblast-like synoviocytes
title_short Role of the NLRP3 inflammasome in the transient release of IL-1β induced by monosodium urate crystals in human fibroblast-like synoviocytes
title_sort role of the nlrp3 inflammasome in the transient release of il-1β induced by monosodium urate crystals in human fibroblast-like synoviocytes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403983/
https://www.ncbi.nlm.nih.gov/pubmed/25897296
http://dx.doi.org/10.1186/s12950-015-0070-7
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