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NLRP3 Inflammasome Activation Regulates Aged RBC Clearance
The NLR family pyrin domain-containing protein 3 (NLRP3) inflammasome is triggered by various stimuli. Whether the NLRP3 inflammasome is activated during the monocyte clearing of aged or damaged erythrocytes is unknown. This work aimed to determine whether the NLRP3 inflammasome is activated during...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061012/ https://www.ncbi.nlm.nih.gov/pubmed/29680907 http://dx.doi.org/10.1007/s10753-018-0784-9 |
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author | Qin, Li Fengyong, Zhao Jiamin, Zhang Qixiu, Yang Geming, Lu Rongwei, Xia Ziyan, Zhu |
author_facet | Qin, Li Fengyong, Zhao Jiamin, Zhang Qixiu, Yang Geming, Lu Rongwei, Xia Ziyan, Zhu |
author_sort | Qin, Li |
collection | PubMed |
description | The NLR family pyrin domain-containing protein 3 (NLRP3) inflammasome is triggered by various stimuli. Whether the NLRP3 inflammasome is activated during the monocyte clearing of aged or damaged erythrocytes is unknown. This work aimed to determine whether the NLRP3 inflammasome is activated during the THP-1 cell engulfing of aged erythrocytes. In the study, THP-1 cells were treated with PMA and then coincubated with untreated red blood cells (RBCs), 42 °C-treated RBCs, immunoglobulin G (IgG) anti-D-sensitized RBCs, Rhnull/Rhmod RBC sample, hemoglobin, and RBC ghost. The activation of the NLRP3 inflammasome and production of some proinflammatory cytokines were determined using immunoblotting, cytometric bead array, and digital PCR. An NLRP3 inflammasome inhibitor was also used to evaluate the alteration of the NLRP3 activation and RBC clearance rate. The untreated RBCs, 42 °C-incubated RBCs, IgG-opsonized RBCs, Rhnull/Rhmod RBCs, RBC ghosts, and hemoglobin induced the THP-1-cell-mediated activation of the NLRP3 inflammasome and the production of inflammatory cytokines. The RBC clearance rate exhibited a positive correlation with the expression of proinflammatory cytokines. The NLRP3 inflammasome inhibitor reduced the NLRP3 activation and RBC phagocytosis rate. The NLRP3 inflammasome was activated during the clearance of the aged erythrocytes through unopsonized and opsonized pathways. However, the mechanism of such phenomenon needs to be further elucidated. Such mechanism may provide new insight into the assessment of the safety of transfusing long-storage RBC based on cytokine levels. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10753-018-0784-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6061012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-60610122018-08-09 NLRP3 Inflammasome Activation Regulates Aged RBC Clearance Qin, Li Fengyong, Zhao Jiamin, Zhang Qixiu, Yang Geming, Lu Rongwei, Xia Ziyan, Zhu Inflammation Original Article The NLR family pyrin domain-containing protein 3 (NLRP3) inflammasome is triggered by various stimuli. Whether the NLRP3 inflammasome is activated during the monocyte clearing of aged or damaged erythrocytes is unknown. This work aimed to determine whether the NLRP3 inflammasome is activated during the THP-1 cell engulfing of aged erythrocytes. In the study, THP-1 cells were treated with PMA and then coincubated with untreated red blood cells (RBCs), 42 °C-treated RBCs, immunoglobulin G (IgG) anti-D-sensitized RBCs, Rhnull/Rhmod RBC sample, hemoglobin, and RBC ghost. The activation of the NLRP3 inflammasome and production of some proinflammatory cytokines were determined using immunoblotting, cytometric bead array, and digital PCR. An NLRP3 inflammasome inhibitor was also used to evaluate the alteration of the NLRP3 activation and RBC clearance rate. The untreated RBCs, 42 °C-incubated RBCs, IgG-opsonized RBCs, Rhnull/Rhmod RBCs, RBC ghosts, and hemoglobin induced the THP-1-cell-mediated activation of the NLRP3 inflammasome and the production of inflammatory cytokines. The RBC clearance rate exhibited a positive correlation with the expression of proinflammatory cytokines. The NLRP3 inflammasome inhibitor reduced the NLRP3 activation and RBC phagocytosis rate. The NLRP3 inflammasome was activated during the clearance of the aged erythrocytes through unopsonized and opsonized pathways. However, the mechanism of such phenomenon needs to be further elucidated. Such mechanism may provide new insight into the assessment of the safety of transfusing long-storage RBC based on cytokine levels. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10753-018-0784-9) contains supplementary material, which is available to authorized users. Springer US 2018-04-21 2018 /pmc/articles/PMC6061012/ /pubmed/29680907 http://dx.doi.org/10.1007/s10753-018-0784-9 Text en © The Author(s) 2018 Open Access This 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. |
spellingShingle | Original Article Qin, Li Fengyong, Zhao Jiamin, Zhang Qixiu, Yang Geming, Lu Rongwei, Xia Ziyan, Zhu NLRP3 Inflammasome Activation Regulates Aged RBC Clearance |
title | NLRP3 Inflammasome Activation Regulates Aged RBC Clearance |
title_full | NLRP3 Inflammasome Activation Regulates Aged RBC Clearance |
title_fullStr | NLRP3 Inflammasome Activation Regulates Aged RBC Clearance |
title_full_unstemmed | NLRP3 Inflammasome Activation Regulates Aged RBC Clearance |
title_short | NLRP3 Inflammasome Activation Regulates Aged RBC Clearance |
title_sort | nlrp3 inflammasome activation regulates aged rbc clearance |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061012/ https://www.ncbi.nlm.nih.gov/pubmed/29680907 http://dx.doi.org/10.1007/s10753-018-0784-9 |
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