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Increased expression of the NLRP3 inflammasome components in patients with Behçet’s disease
BACKGROUND: Behçet’s disease (BD) is a systemic inflammatory disease with manifestations including recurrent oral and genital ulcerations, and vasculitis involving the skin, mucosa, joints, eyes, veins, arteries, nervous and gastrointestinal systems. BD is seen as a disease at the crossroad between...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487834/ https://www.ncbi.nlm.nih.gov/pubmed/26136643 http://dx.doi.org/10.1186/s12950-015-0086-z |
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author | Kim, En Hyung Park, Mi-Jin Park, Sun Lee, Eun-So |
author_facet | Kim, En Hyung Park, Mi-Jin Park, Sun Lee, Eun-So |
author_sort | Kim, En Hyung |
collection | PubMed |
description | BACKGROUND: Behçet’s disease (BD) is a systemic inflammatory disease with manifestations including recurrent oral and genital ulcerations, and vasculitis involving the skin, mucosa, joints, eyes, veins, arteries, nervous and gastrointestinal systems. BD is seen as a disease at the crossroad between autoimmune and autoinflammatory syndromes, possibly triggered by an aberrant response to infectious stimuli. The relevance of Gram negative bacteria-mediated oral inflammation with the increased expression of NACHT, LRR, and PYD domains-containing protein 3 (NLRP3), leading to systemic inflammation, prompted us to investigate the expression of NLRP3 inflammasome components and its link with IL-1β hypersecretion. FINDINGS: When peripheral blood mononuclear cells (PBMCs) from 15 active, 15 stable BD patients and 15 healthy volunteers were stimulated, the basal and LPS-induced expressions of NLRP3 inflammasome components were significantly increased at both mRNA and protein levels in BD patients compared to healthy controls. Also, increased expression of NLRP3 and ASC was observed in 25 BD skin lesions compared to 25 erythema nodosum patients. Compatible with this, secretion of IL-1β by PBMCs stimulated with LPS alone or LPS plus ATP was increased in BD compared to healthy controls, which was suppressed by caspase-1 inhibitor. CONCLUSION: Our findings suggest the possible link between increased IL-1β secretion and increased expression of NLRP3 inflammasome components in BD patients with skin manifestations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12950-015-0086-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4487834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44878342015-07-02 Increased expression of the NLRP3 inflammasome components in patients with Behçet’s disease Kim, En Hyung Park, Mi-Jin Park, Sun Lee, Eun-So J Inflamm (Lond) Short Report BACKGROUND: Behçet’s disease (BD) is a systemic inflammatory disease with manifestations including recurrent oral and genital ulcerations, and vasculitis involving the skin, mucosa, joints, eyes, veins, arteries, nervous and gastrointestinal systems. BD is seen as a disease at the crossroad between autoimmune and autoinflammatory syndromes, possibly triggered by an aberrant response to infectious stimuli. The relevance of Gram negative bacteria-mediated oral inflammation with the increased expression of NACHT, LRR, and PYD domains-containing protein 3 (NLRP3), leading to systemic inflammation, prompted us to investigate the expression of NLRP3 inflammasome components and its link with IL-1β hypersecretion. FINDINGS: When peripheral blood mononuclear cells (PBMCs) from 15 active, 15 stable BD patients and 15 healthy volunteers were stimulated, the basal and LPS-induced expressions of NLRP3 inflammasome components were significantly increased at both mRNA and protein levels in BD patients compared to healthy controls. Also, increased expression of NLRP3 and ASC was observed in 25 BD skin lesions compared to 25 erythema nodosum patients. Compatible with this, secretion of IL-1β by PBMCs stimulated with LPS alone or LPS plus ATP was increased in BD compared to healthy controls, which was suppressed by caspase-1 inhibitor. CONCLUSION: Our findings suggest the possible link between increased IL-1β secretion and increased expression of NLRP3 inflammasome components in BD patients with skin manifestations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12950-015-0086-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-02 /pmc/articles/PMC4487834/ /pubmed/26136643 http://dx.doi.org/10.1186/s12950-015-0086-z Text en © Kim et al. 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 | Short Report Kim, En Hyung Park, Mi-Jin Park, Sun Lee, Eun-So Increased expression of the NLRP3 inflammasome components in patients with Behçet’s disease |
title | Increased expression of the NLRP3 inflammasome components in patients with Behçet’s disease |
title_full | Increased expression of the NLRP3 inflammasome components in patients with Behçet’s disease |
title_fullStr | Increased expression of the NLRP3 inflammasome components in patients with Behçet’s disease |
title_full_unstemmed | Increased expression of the NLRP3 inflammasome components in patients with Behçet’s disease |
title_short | Increased expression of the NLRP3 inflammasome components in patients with Behçet’s disease |
title_sort | increased expression of the nlrp3 inflammasome components in patients with behçet’s disease |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487834/ https://www.ncbi.nlm.nih.gov/pubmed/26136643 http://dx.doi.org/10.1186/s12950-015-0086-z |
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