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NLRP3+ macrophages aggravate inflammatory cystitis in diabetes

Inflammatory macrophages play a pivotal role in the progression of inflammatory cystitis. Formation of NOD-, LRR- and PYD domains-containing protein 3 (NLRP3) inflammasome triggers the activation of caspase-1/IL-1β signaling cascades to mediate inflammatory response. However, it is not known whether...

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Autores principales: Peng, Yubing, Gao, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668889/
https://www.ncbi.nlm.nih.gov/pubmed/36405726
http://dx.doi.org/10.3389/fimmu.2022.1057746
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author Peng, Yubing
Gao, Yan
author_facet Peng, Yubing
Gao, Yan
author_sort Peng, Yubing
collection PubMed
description Inflammatory macrophages play a pivotal role in the progression of inflammatory cystitis. Formation of NOD-, LRR- and PYD domains-containing protein 3 (NLRP3) inflammasome triggers the activation of caspase-1/IL-1β signaling cascades to mediate inflammatory response. However, it is not known whether NLRP3 activation in macrophages during cystitis may differ in normal or diabetic setting as well as the importance of it. In this study, we found that NLRP3 levels significantly increased in bladder macrophages in diabetic mice that underwent cystitis. Moreover, bladder macrophages from diabetic mice appeared to have increased their potential of growth, migration and phagocytosis. Furthermore, specific depletion of NLRP3 in macrophages alleviated the severity of cystitis in diabetic mice, but not in non-diabetic mice. Together, our data suggest that NLRP3 depletion in macrophages may be a promising strategy for treating diabetic cystitis.
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spelling pubmed-96688892022-11-18 NLRP3+ macrophages aggravate inflammatory cystitis in diabetes Peng, Yubing Gao, Yan Front Immunol Immunology Inflammatory macrophages play a pivotal role in the progression of inflammatory cystitis. Formation of NOD-, LRR- and PYD domains-containing protein 3 (NLRP3) inflammasome triggers the activation of caspase-1/IL-1β signaling cascades to mediate inflammatory response. However, it is not known whether NLRP3 activation in macrophages during cystitis may differ in normal or diabetic setting as well as the importance of it. In this study, we found that NLRP3 levels significantly increased in bladder macrophages in diabetic mice that underwent cystitis. Moreover, bladder macrophages from diabetic mice appeared to have increased their potential of growth, migration and phagocytosis. Furthermore, specific depletion of NLRP3 in macrophages alleviated the severity of cystitis in diabetic mice, but not in non-diabetic mice. Together, our data suggest that NLRP3 depletion in macrophages may be a promising strategy for treating diabetic cystitis. Frontiers Media S.A. 2022-11-03 /pmc/articles/PMC9668889/ /pubmed/36405726 http://dx.doi.org/10.3389/fimmu.2022.1057746 Text en Copyright © 2022 Peng and Gao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Peng, Yubing
Gao, Yan
NLRP3+ macrophages aggravate inflammatory cystitis in diabetes
title NLRP3+ macrophages aggravate inflammatory cystitis in diabetes
title_full NLRP3+ macrophages aggravate inflammatory cystitis in diabetes
title_fullStr NLRP3+ macrophages aggravate inflammatory cystitis in diabetes
title_full_unstemmed NLRP3+ macrophages aggravate inflammatory cystitis in diabetes
title_short NLRP3+ macrophages aggravate inflammatory cystitis in diabetes
title_sort nlrp3+ macrophages aggravate inflammatory cystitis in diabetes
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668889/
https://www.ncbi.nlm.nih.gov/pubmed/36405726
http://dx.doi.org/10.3389/fimmu.2022.1057746
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