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Elevated microRNA-21 Is a Brake of Inflammation Involved in the Development of Nasal Polyps

BACKGROUND: CRSwNP is an inflammatory disease but the mechanism is not yet fully understood. MiR-21, a member of miRNAs, has been reported to play roles in mediating inflammation. However, the expression of miR-21 and its role in patients with CRSwNP remain elusive. METHODS: Turbinates from control...

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Autores principales: Liu, Ruowu, Du, Jintao, Zhou, Jiao, Zhong, Bing, Ba, Luo, Zhang, Jie, Liu, Yafeng, Liu, Shixi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082185/
https://www.ncbi.nlm.nih.gov/pubmed/33936025
http://dx.doi.org/10.3389/fimmu.2021.530488
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author Liu, Ruowu
Du, Jintao
Zhou, Jiao
Zhong, Bing
Ba, Luo
Zhang, Jie
Liu, Yafeng
Liu, Shixi
author_facet Liu, Ruowu
Du, Jintao
Zhou, Jiao
Zhong, Bing
Ba, Luo
Zhang, Jie
Liu, Yafeng
Liu, Shixi
author_sort Liu, Ruowu
collection PubMed
description BACKGROUND: CRSwNP is an inflammatory disease but the mechanism is not yet fully understood. MiR-21, a member of miRNAs, has been reported to play roles in mediating inflammation. However, the expression of miR-21 and its role in patients with CRSwNP remain elusive. METHODS: Turbinates from control subjects, uncinate processes from CRSsNP, polyp tissues from CRSwNP, and nasal epithelial cells brushed from nasal mucosa were collected. The expression of miR-21 and cytokines in nasal tissues and epithelial cells were detected by qPCR. The localization of miR-21 was detected by ISH, and its target was identified by bioinformation analysis, qPCR, IHC, WB, and luciferase reporter system. The protein and mRNA of PDCD4 and NF-κB P65 were determined by WB and qPCR after miR-21 transfection in HNEpC. The role of miR-21 on cytokines was analyzed in HNEpC and nasal polyp explants. RESULTS: MiR-21 was upregulated in CRSwNP relative to control subjects by qPCR, which was determined mainly in nasal epithelial cells of CRSwNP by ISH. Both pro-inflammation cytokines (IL-1β, IL-6, IL-8, IL-25, and TSLP) and a suppressive cytokine (IL-10) were overexpressed in the epithelial cells of CRSwNP. The expression of miR-21 was positively correlated with IL-10 and negatively correlated with IL-6, IL-8, IL-33, and TSLP in the epithelial cells of CRSwNP. As a potential target of miR-21, the expression of PDCD4 was negatively correlated with miR-21 in CRSwNP. In HNEpC, miR-21 could reduce the expression of PDCD4 at both mRNA and protein levels, and bioinformation analysis and luciferase reporter system confirmed PDCD4 as one target of miR-21. Furthermore, miR-21 could decrease the activation of NF-κB and increase IL-10 mRNA. Both SEB and LPS could elevate miR-21, with IL-25, IL-33, TSLP induced by SEB and IL-1β, IL-6, IL-8 induced by LPS, while the miR-21 could regulate the expression of IL-33, TSLP, IL-1β, IL- 6 and IL-8 in vitro and ex vivo. Clinically, miR-21 expression was inversely correlated with the Lund-Mackay CT scores and the Lund-Kennedy scores in CRSwNP. CONCLUSION: MiR-21 could be a prominent negative feedback factor in the inflammation process to attenuate the expression of pro-inflammatory cytokines, thereby playing an anti-inflammation role in CRSwNP.
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spelling pubmed-80821852021-04-30 Elevated microRNA-21 Is a Brake of Inflammation Involved in the Development of Nasal Polyps Liu, Ruowu Du, Jintao Zhou, Jiao Zhong, Bing Ba, Luo Zhang, Jie Liu, Yafeng Liu, Shixi Front Immunol Immunology BACKGROUND: CRSwNP is an inflammatory disease but the mechanism is not yet fully understood. MiR-21, a member of miRNAs, has been reported to play roles in mediating inflammation. However, the expression of miR-21 and its role in patients with CRSwNP remain elusive. METHODS: Turbinates from control subjects, uncinate processes from CRSsNP, polyp tissues from CRSwNP, and nasal epithelial cells brushed from nasal mucosa were collected. The expression of miR-21 and cytokines in nasal tissues and epithelial cells were detected by qPCR. The localization of miR-21 was detected by ISH, and its target was identified by bioinformation analysis, qPCR, IHC, WB, and luciferase reporter system. The protein and mRNA of PDCD4 and NF-κB P65 were determined by WB and qPCR after miR-21 transfection in HNEpC. The role of miR-21 on cytokines was analyzed in HNEpC and nasal polyp explants. RESULTS: MiR-21 was upregulated in CRSwNP relative to control subjects by qPCR, which was determined mainly in nasal epithelial cells of CRSwNP by ISH. Both pro-inflammation cytokines (IL-1β, IL-6, IL-8, IL-25, and TSLP) and a suppressive cytokine (IL-10) were overexpressed in the epithelial cells of CRSwNP. The expression of miR-21 was positively correlated with IL-10 and negatively correlated with IL-6, IL-8, IL-33, and TSLP in the epithelial cells of CRSwNP. As a potential target of miR-21, the expression of PDCD4 was negatively correlated with miR-21 in CRSwNP. In HNEpC, miR-21 could reduce the expression of PDCD4 at both mRNA and protein levels, and bioinformation analysis and luciferase reporter system confirmed PDCD4 as one target of miR-21. Furthermore, miR-21 could decrease the activation of NF-κB and increase IL-10 mRNA. Both SEB and LPS could elevate miR-21, with IL-25, IL-33, TSLP induced by SEB and IL-1β, IL-6, IL-8 induced by LPS, while the miR-21 could regulate the expression of IL-33, TSLP, IL-1β, IL- 6 and IL-8 in vitro and ex vivo. Clinically, miR-21 expression was inversely correlated with the Lund-Mackay CT scores and the Lund-Kennedy scores in CRSwNP. CONCLUSION: MiR-21 could be a prominent negative feedback factor in the inflammation process to attenuate the expression of pro-inflammatory cytokines, thereby playing an anti-inflammation role in CRSwNP. Frontiers Media S.A. 2021-04-15 /pmc/articles/PMC8082185/ /pubmed/33936025 http://dx.doi.org/10.3389/fimmu.2021.530488 Text en Copyright © 2021 Liu, Du, Zhou, Zhong, Ba, Zhang, Liu and Liu 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
Liu, Ruowu
Du, Jintao
Zhou, Jiao
Zhong, Bing
Ba, Luo
Zhang, Jie
Liu, Yafeng
Liu, Shixi
Elevated microRNA-21 Is a Brake of Inflammation Involved in the Development of Nasal Polyps
title Elevated microRNA-21 Is a Brake of Inflammation Involved in the Development of Nasal Polyps
title_full Elevated microRNA-21 Is a Brake of Inflammation Involved in the Development of Nasal Polyps
title_fullStr Elevated microRNA-21 Is a Brake of Inflammation Involved in the Development of Nasal Polyps
title_full_unstemmed Elevated microRNA-21 Is a Brake of Inflammation Involved in the Development of Nasal Polyps
title_short Elevated microRNA-21 Is a Brake of Inflammation Involved in the Development of Nasal Polyps
title_sort elevated microrna-21 is a brake of inflammation involved in the development of nasal polyps
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082185/
https://www.ncbi.nlm.nih.gov/pubmed/33936025
http://dx.doi.org/10.3389/fimmu.2021.530488
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