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The role of miR-29c/B7-H3 axis in children with allergic asthma
BACKGROUND: MicroRNAs play roles in the pathogenesis of bronchial asthma. However, the mechanism of miR-29c in allergic asthma remains unclear. This study is to elucidate the regulation of Th cell differentiation by miR-29c in mononuclear macrophages. METHODS: A total of 52 children with asthma exac...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6076420/ https://www.ncbi.nlm.nih.gov/pubmed/30075787 http://dx.doi.org/10.1186/s12967-018-1590-8 |
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author | Zhang, Xinxing Zhao, Xin Sun, Huiming Yan, Yongdong Huang, Li Gu, Wenjin Jiang, Wujun Wang, Yuqing Zhu, Canhong Ji, Wei Hao, Chuangli Chen, Zhengrong |
author_facet | Zhang, Xinxing Zhao, Xin Sun, Huiming Yan, Yongdong Huang, Li Gu, Wenjin Jiang, Wujun Wang, Yuqing Zhu, Canhong Ji, Wei Hao, Chuangli Chen, Zhengrong |
author_sort | Zhang, Xinxing |
collection | PubMed |
description | BACKGROUND: MicroRNAs play roles in the pathogenesis of bronchial asthma. However, the mechanism of miR-29c in allergic asthma remains unclear. This study is to elucidate the regulation of Th cell differentiation by miR-29c in mononuclear macrophages. METHODS: A total of 52 children with asthma exacerbation and 26 children as controls were enrolled in the study. CD14(+) monocytes were isolated from the peripheral blood. Differential expressions of microRNAs were evaluated using microarray analysis and miR-29c expression in monocytes was determined by qRT-PCR. The plasma B7-H3 was determined by ELISA. Transfection studies and luciferase reporter assay were performed to confirm target gene of miR-29c and its function. RESULTS: Compared to controls, 88 miRNAs in blood monocytes were up-regulated and 41 miRNAs down-regulated including miR-29c in asthma children. Children with asthma exacerbation had significantly lower level of miR-29c and higher level of plasma B7-H3 compared to controls (both P < 0.05). Functional studies based on luciferase reporter assay and immunofluorescence staining suggest that B7-H3 is the direct target of miR-29c and transfection anti-miR-29c into macrophages could enhance ROR-γt and GATA-3 expression in co-cultured CD4(+) T cells and increase levels of IL-4 and IL-17 in supernatants. CONCLUSION: The axis of miR-29c/B7-H3 plays an important role in children with asthma through regulating Th2/Th17 cell differentiation and may provide new targets for treatment of asthma. |
format | Online Article Text |
id | pubmed-6076420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60764202018-08-07 The role of miR-29c/B7-H3 axis in children with allergic asthma Zhang, Xinxing Zhao, Xin Sun, Huiming Yan, Yongdong Huang, Li Gu, Wenjin Jiang, Wujun Wang, Yuqing Zhu, Canhong Ji, Wei Hao, Chuangli Chen, Zhengrong J Transl Med Research BACKGROUND: MicroRNAs play roles in the pathogenesis of bronchial asthma. However, the mechanism of miR-29c in allergic asthma remains unclear. This study is to elucidate the regulation of Th cell differentiation by miR-29c in mononuclear macrophages. METHODS: A total of 52 children with asthma exacerbation and 26 children as controls were enrolled in the study. CD14(+) monocytes were isolated from the peripheral blood. Differential expressions of microRNAs were evaluated using microarray analysis and miR-29c expression in monocytes was determined by qRT-PCR. The plasma B7-H3 was determined by ELISA. Transfection studies and luciferase reporter assay were performed to confirm target gene of miR-29c and its function. RESULTS: Compared to controls, 88 miRNAs in blood monocytes were up-regulated and 41 miRNAs down-regulated including miR-29c in asthma children. Children with asthma exacerbation had significantly lower level of miR-29c and higher level of plasma B7-H3 compared to controls (both P < 0.05). Functional studies based on luciferase reporter assay and immunofluorescence staining suggest that B7-H3 is the direct target of miR-29c and transfection anti-miR-29c into macrophages could enhance ROR-γt and GATA-3 expression in co-cultured CD4(+) T cells and increase levels of IL-4 and IL-17 in supernatants. CONCLUSION: The axis of miR-29c/B7-H3 plays an important role in children with asthma through regulating Th2/Th17 cell differentiation and may provide new targets for treatment of asthma. BioMed Central 2018-08-03 /pmc/articles/PMC6076420/ /pubmed/30075787 http://dx.doi.org/10.1186/s12967-018-1590-8 Text en © The Author(s) 2018 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 | Research Zhang, Xinxing Zhao, Xin Sun, Huiming Yan, Yongdong Huang, Li Gu, Wenjin Jiang, Wujun Wang, Yuqing Zhu, Canhong Ji, Wei Hao, Chuangli Chen, Zhengrong The role of miR-29c/B7-H3 axis in children with allergic asthma |
title | The role of miR-29c/B7-H3 axis in children with allergic asthma |
title_full | The role of miR-29c/B7-H3 axis in children with allergic asthma |
title_fullStr | The role of miR-29c/B7-H3 axis in children with allergic asthma |
title_full_unstemmed | The role of miR-29c/B7-H3 axis in children with allergic asthma |
title_short | The role of miR-29c/B7-H3 axis in children with allergic asthma |
title_sort | role of mir-29c/b7-h3 axis in children with allergic asthma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6076420/ https://www.ncbi.nlm.nih.gov/pubmed/30075787 http://dx.doi.org/10.1186/s12967-018-1590-8 |
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