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Gene expression of inflammasome components in peripheral blood mononuclear cells (PBMC) of vascular patients increases with age

BACKGROUND: Chronic low-grade inflammation is considered a driver of many age-related disorders, including vascular diseases (inflammaging). Inhibition of autophagic capacity with ageing was postulated to generate a pro-inflammatory condition via activation of inflammasomes, a group of Interleukin-1...

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Autores principales: Wu, Xiaoyu, Hakimi, Maani, Wortmann, Markus, Zhang, Jian, Böckler, Dittmar, Dihlmann, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596365/
https://www.ncbi.nlm.nih.gov/pubmed/26448778
http://dx.doi.org/10.1186/s12979-015-0043-y
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author Wu, Xiaoyu
Hakimi, Maani
Wortmann, Markus
Zhang, Jian
Böckler, Dittmar
Dihlmann, Susanne
author_facet Wu, Xiaoyu
Hakimi, Maani
Wortmann, Markus
Zhang, Jian
Böckler, Dittmar
Dihlmann, Susanne
author_sort Wu, Xiaoyu
collection PubMed
description BACKGROUND: Chronic low-grade inflammation is considered a driver of many age-related disorders, including vascular diseases (inflammaging). Inhibition of autophagic capacity with ageing was postulated to generate a pro-inflammatory condition via activation of inflammasomes, a group of Interleukin-1 activating intracellular multi-protein complexes. We thus investigated gene expression of inflammasome components in PBMC of 77 vascular patients (age 22–82) in association with age. FINDINGS: Linear regression of real-time qRT-PCR data revealed a significant positive association of gene expression of each of the inflammasome components with age (Pearson correlation coefficients: AIM2: r = 0.245; P = 0.032; NLRP3: r = 0.367; P = 0.001; ASC (PYCARD): r = 0.252; P = 0.027; CASP1: r = 0.296; P = 0.009; CASP5: r = 0.453; P = 0.00003; IL1B: r = 0.247; P = 0.030). No difference in gene expression of AIM2, NLRP3, ASC CASP1, and CASP5 was detected between PBMC of patients with advanced atherosclerosis and other vascular patients, whereas IL1B expression was increased in PBMC of the latter group (P = 0.0005). CONCLUSION: The findings reinforce the systemic pro-inflammatory phenotype reported in elderly by demonstrating an increased phase-1 activation of inflammasomes in PBMC of vascular patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12979-015-0043-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-45963652015-10-08 Gene expression of inflammasome components in peripheral blood mononuclear cells (PBMC) of vascular patients increases with age Wu, Xiaoyu Hakimi, Maani Wortmann, Markus Zhang, Jian Böckler, Dittmar Dihlmann, Susanne Immun Ageing Short Report BACKGROUND: Chronic low-grade inflammation is considered a driver of many age-related disorders, including vascular diseases (inflammaging). Inhibition of autophagic capacity with ageing was postulated to generate a pro-inflammatory condition via activation of inflammasomes, a group of Interleukin-1 activating intracellular multi-protein complexes. We thus investigated gene expression of inflammasome components in PBMC of 77 vascular patients (age 22–82) in association with age. FINDINGS: Linear regression of real-time qRT-PCR data revealed a significant positive association of gene expression of each of the inflammasome components with age (Pearson correlation coefficients: AIM2: r = 0.245; P = 0.032; NLRP3: r = 0.367; P = 0.001; ASC (PYCARD): r = 0.252; P = 0.027; CASP1: r = 0.296; P = 0.009; CASP5: r = 0.453; P = 0.00003; IL1B: r = 0.247; P = 0.030). No difference in gene expression of AIM2, NLRP3, ASC CASP1, and CASP5 was detected between PBMC of patients with advanced atherosclerosis and other vascular patients, whereas IL1B expression was increased in PBMC of the latter group (P = 0.0005). CONCLUSION: The findings reinforce the systemic pro-inflammatory phenotype reported in elderly by demonstrating an increased phase-1 activation of inflammasomes in PBMC of vascular patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12979-015-0043-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-06 /pmc/articles/PMC4596365/ /pubmed/26448778 http://dx.doi.org/10.1186/s12979-015-0043-y Text en © Wu et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Wu, Xiaoyu
Hakimi, Maani
Wortmann, Markus
Zhang, Jian
Böckler, Dittmar
Dihlmann, Susanne
Gene expression of inflammasome components in peripheral blood mononuclear cells (PBMC) of vascular patients increases with age
title Gene expression of inflammasome components in peripheral blood mononuclear cells (PBMC) of vascular patients increases with age
title_full Gene expression of inflammasome components in peripheral blood mononuclear cells (PBMC) of vascular patients increases with age
title_fullStr Gene expression of inflammasome components in peripheral blood mononuclear cells (PBMC) of vascular patients increases with age
title_full_unstemmed Gene expression of inflammasome components in peripheral blood mononuclear cells (PBMC) of vascular patients increases with age
title_short Gene expression of inflammasome components in peripheral blood mononuclear cells (PBMC) of vascular patients increases with age
title_sort gene expression of inflammasome components in peripheral blood mononuclear cells (pbmc) of vascular patients increases with age
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596365/
https://www.ncbi.nlm.nih.gov/pubmed/26448778
http://dx.doi.org/10.1186/s12979-015-0043-y
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