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Role of Genetic Alterations in the NLRP3 and CARD8 Genes in Health and Disease

The complexity of a common inflammatory disease is influenced by multiple genetic and environmental factors contributing to the susceptibility of disease. Studies have reported that these exogenous and endogenous components may perturb the balance of innate immune response by activating the NLRP3 in...

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Detalles Bibliográficos
Autores principales: Paramel, G. V., Sirsjö, A., Fransén, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348606/
https://www.ncbi.nlm.nih.gov/pubmed/25788762
http://dx.doi.org/10.1155/2015/846782
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author Paramel, G. V.
Sirsjö, A.
Fransén, K.
author_facet Paramel, G. V.
Sirsjö, A.
Fransén, K.
author_sort Paramel, G. V.
collection PubMed
description The complexity of a common inflammatory disease is influenced by multiple genetic and environmental factors contributing to the susceptibility of disease. Studies have reported that these exogenous and endogenous components may perturb the balance of innate immune response by activating the NLRP3 inflammasome. The multimeric NLRP3 complex results in the caspase-1 activation and the release of potent inflammatory cytokines, like IL-1β. Several studies have been performed on the association of the genetic alterations in genes encoding NLRP3 and CARD8 with the complex diseases with inflammatory background, like inflammatory bowel disease, cardiovascular diseases, rheumatoid arthritis, and type 1 diabetes. The aim of the present review is therefore to summarize the literature regarding genetic alterations in these genes and their association with health and disease.
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spelling pubmed-43486062015-03-18 Role of Genetic Alterations in the NLRP3 and CARD8 Genes in Health and Disease Paramel, G. V. Sirsjö, A. Fransén, K. Mediators Inflamm Review Article The complexity of a common inflammatory disease is influenced by multiple genetic and environmental factors contributing to the susceptibility of disease. Studies have reported that these exogenous and endogenous components may perturb the balance of innate immune response by activating the NLRP3 inflammasome. The multimeric NLRP3 complex results in the caspase-1 activation and the release of potent inflammatory cytokines, like IL-1β. Several studies have been performed on the association of the genetic alterations in genes encoding NLRP3 and CARD8 with the complex diseases with inflammatory background, like inflammatory bowel disease, cardiovascular diseases, rheumatoid arthritis, and type 1 diabetes. The aim of the present review is therefore to summarize the literature regarding genetic alterations in these genes and their association with health and disease. Hindawi Publishing Corporation 2015 2015-02-18 /pmc/articles/PMC4348606/ /pubmed/25788762 http://dx.doi.org/10.1155/2015/846782 Text en Copyright © 2015 G. V. Paramel et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Paramel, G. V.
Sirsjö, A.
Fransén, K.
Role of Genetic Alterations in the NLRP3 and CARD8 Genes in Health and Disease
title Role of Genetic Alterations in the NLRP3 and CARD8 Genes in Health and Disease
title_full Role of Genetic Alterations in the NLRP3 and CARD8 Genes in Health and Disease
title_fullStr Role of Genetic Alterations in the NLRP3 and CARD8 Genes in Health and Disease
title_full_unstemmed Role of Genetic Alterations in the NLRP3 and CARD8 Genes in Health and Disease
title_short Role of Genetic Alterations in the NLRP3 and CARD8 Genes in Health and Disease
title_sort role of genetic alterations in the nlrp3 and card8 genes in health and disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348606/
https://www.ncbi.nlm.nih.gov/pubmed/25788762
http://dx.doi.org/10.1155/2015/846782
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