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Comparative Analysis of Differentially Expressed Circular RNAs in Polarized Macrophages

Macrophage polarization is a process that macrophages exert different functions according to surrounding micro-environment. Macrophages commonly exist in two distinct subsets: classically activated M1 macrophages and alternatively activated M2 macrophages. Circular RNAs (circRNAs) are a novel class...

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Autores principales: Zhou, Rong-mei, Shi, Ze-hui, Shan, Kun, Zhang, Shu-jie, Zhang, Yi-han, Liang, Yu, Yan, Biao, Zhao, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967150/
https://www.ncbi.nlm.nih.gov/pubmed/35368656
http://dx.doi.org/10.3389/fgene.2022.823517
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author Zhou, Rong-mei
Shi, Ze-hui
Shan, Kun
Zhang, Shu-jie
Zhang, Yi-han
Liang, Yu
Yan, Biao
Zhao, Chen
author_facet Zhou, Rong-mei
Shi, Ze-hui
Shan, Kun
Zhang, Shu-jie
Zhang, Yi-han
Liang, Yu
Yan, Biao
Zhao, Chen
author_sort Zhou, Rong-mei
collection PubMed
description Macrophage polarization is a process that macrophages exert different functions according to surrounding micro-environment. Macrophages commonly exist in two distinct subsets: classically activated M1 macrophages and alternatively activated M2 macrophages. Circular RNAs (circRNAs) are a novel class of non-coding RNAs generated by back-splicing. Thousands of circRNAs were identified in different cells and tissues. Recent studies have revealed that circRNAs play a crucial role in regulating transcriptional and post-transcriptional gene expression. However, the effects and roles of circRNAs in macrophage polarization have not been well elucidated. Here, circRNAs expression profiles were determined in human THP-1 macrophages incubated in conditions causing activation toward M1 (interferon-γ + LPS) or M2 (interleukin-4) phenotypes. Overall, 9,720 circular RNA were detected from RNA sequencing data. Compared with M2 macrophages, a total of 140 circRNAs were aberrantly expressed in M1 macrophages, including 71 up-regulated circRNAs and 69 down-regulated circRNAs. Quantitative real-time PCR (qRT-PCR) results were generally consistent with the selected differentially expressed circRNAs. Gene Ontology (GO) and KEGG pathway analyses were used to predict biological functions and potential mechanisms of the host linear transcripts of these up-regulated and down-regulated circRNAs. Furthermore, we found that the expression level of circRNA-RNF19B (circRNF19B) in M1 macrophages was significantly higher than that in THP-1 macrophages and M2 macrophages. circRNF19B expression was increased when M2 converted to M1 whereas decreased when M1 converted to M2. Knockdown of circRNF19B following the activation of THP-1 cells using interferon-γ + LPS diminished the expression of M1 macrophages markers and elevated the expression of M2 macrophages markers. In conclusion, these data suggest the involvement of altered circRNAs expression patterns in macrophages exposure to different activating conditions. Circular RNAs may play important roles in regulating macrophage polarization.
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spelling pubmed-89671502022-03-31 Comparative Analysis of Differentially Expressed Circular RNAs in Polarized Macrophages Zhou, Rong-mei Shi, Ze-hui Shan, Kun Zhang, Shu-jie Zhang, Yi-han Liang, Yu Yan, Biao Zhao, Chen Front Genet Genetics Macrophage polarization is a process that macrophages exert different functions according to surrounding micro-environment. Macrophages commonly exist in two distinct subsets: classically activated M1 macrophages and alternatively activated M2 macrophages. Circular RNAs (circRNAs) are a novel class of non-coding RNAs generated by back-splicing. Thousands of circRNAs were identified in different cells and tissues. Recent studies have revealed that circRNAs play a crucial role in regulating transcriptional and post-transcriptional gene expression. However, the effects and roles of circRNAs in macrophage polarization have not been well elucidated. Here, circRNAs expression profiles were determined in human THP-1 macrophages incubated in conditions causing activation toward M1 (interferon-γ + LPS) or M2 (interleukin-4) phenotypes. Overall, 9,720 circular RNA were detected from RNA sequencing data. Compared with M2 macrophages, a total of 140 circRNAs were aberrantly expressed in M1 macrophages, including 71 up-regulated circRNAs and 69 down-regulated circRNAs. Quantitative real-time PCR (qRT-PCR) results were generally consistent with the selected differentially expressed circRNAs. Gene Ontology (GO) and KEGG pathway analyses were used to predict biological functions and potential mechanisms of the host linear transcripts of these up-regulated and down-regulated circRNAs. Furthermore, we found that the expression level of circRNA-RNF19B (circRNF19B) in M1 macrophages was significantly higher than that in THP-1 macrophages and M2 macrophages. circRNF19B expression was increased when M2 converted to M1 whereas decreased when M1 converted to M2. Knockdown of circRNF19B following the activation of THP-1 cells using interferon-γ + LPS diminished the expression of M1 macrophages markers and elevated the expression of M2 macrophages markers. In conclusion, these data suggest the involvement of altered circRNAs expression patterns in macrophages exposure to different activating conditions. Circular RNAs may play important roles in regulating macrophage polarization. Frontiers Media S.A. 2022-03-16 /pmc/articles/PMC8967150/ /pubmed/35368656 http://dx.doi.org/10.3389/fgene.2022.823517 Text en Copyright © 2022 Zhou, Shi, Shan, Zhang, Zhang, Liang, Yan and Zhao. 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 Genetics
Zhou, Rong-mei
Shi, Ze-hui
Shan, Kun
Zhang, Shu-jie
Zhang, Yi-han
Liang, Yu
Yan, Biao
Zhao, Chen
Comparative Analysis of Differentially Expressed Circular RNAs in Polarized Macrophages
title Comparative Analysis of Differentially Expressed Circular RNAs in Polarized Macrophages
title_full Comparative Analysis of Differentially Expressed Circular RNAs in Polarized Macrophages
title_fullStr Comparative Analysis of Differentially Expressed Circular RNAs in Polarized Macrophages
title_full_unstemmed Comparative Analysis of Differentially Expressed Circular RNAs in Polarized Macrophages
title_short Comparative Analysis of Differentially Expressed Circular RNAs in Polarized Macrophages
title_sort comparative analysis of differentially expressed circular rnas in polarized macrophages
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967150/
https://www.ncbi.nlm.nih.gov/pubmed/35368656
http://dx.doi.org/10.3389/fgene.2022.823517
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