Cargando…

Inhibition of EZH2 Causes Retrotransposon Derepression and Immune Activation in Porcine Lung Alveolar Macrophages

Alveolar macrophages (AMs) form the first defense line against various respiratory pathogens, and their immune response has a profound impact on the outcome of respiratory infection. Enhancer of zeste homolog 2 (EZH2), which catalyzes the trimethylation of H3K27 for epigenetic repression, has gained...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Liangliang, Jin, Jian, Qin, Weiyun, Jiang, Jing, Bao, Wenbin, Sun, Ming-an
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917017/
https://www.ncbi.nlm.nih.gov/pubmed/36768720
http://dx.doi.org/10.3390/ijms24032394
_version_ 1784886267861794816
author Zhang, Liangliang
Jin, Jian
Qin, Weiyun
Jiang, Jing
Bao, Wenbin
Sun, Ming-an
author_facet Zhang, Liangliang
Jin, Jian
Qin, Weiyun
Jiang, Jing
Bao, Wenbin
Sun, Ming-an
author_sort Zhang, Liangliang
collection PubMed
description Alveolar macrophages (AMs) form the first defense line against various respiratory pathogens, and their immune response has a profound impact on the outcome of respiratory infection. Enhancer of zeste homolog 2 (EZH2), which catalyzes the trimethylation of H3K27 for epigenetic repression, has gained increasing attention for its immune regulation function, yet its exact function in AMs remains largely obscure. Using porcine 3D4/21 AM cells as a model, we characterized the transcriptomic and epigenomic alterations after the inhibition of EZH2. We found that the inhibition of EZH2 causes transcriptional activation of numerous immune genes and inhibits the subsequent infection by influenza A virus. Interestingly, specific families of transposable elements, particularly endogenous retrovirus elements (ERVs) and LINEs which belong to retrotransposons, also become derepressed. While some of the derepressed ERV families are pig-specific, a few ancestral families are known to be under EZH2-mediated repression in humans. Given that derepression of ERVs can promote innate immune activation through “viral mimicry”, we speculate that ERVs may also contribute to the coinciding immune activation in AMs after the inhibition of EZH2. Overall, this study improves the understanding of the EZH2-related immune regulation in AMs and provides novel insights into the epigenetic regulation of retrotransposons in pigs.
format Online
Article
Text
id pubmed-9917017
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-99170172023-02-11 Inhibition of EZH2 Causes Retrotransposon Derepression and Immune Activation in Porcine Lung Alveolar Macrophages Zhang, Liangliang Jin, Jian Qin, Weiyun Jiang, Jing Bao, Wenbin Sun, Ming-an Int J Mol Sci Article Alveolar macrophages (AMs) form the first defense line against various respiratory pathogens, and their immune response has a profound impact on the outcome of respiratory infection. Enhancer of zeste homolog 2 (EZH2), which catalyzes the trimethylation of H3K27 for epigenetic repression, has gained increasing attention for its immune regulation function, yet its exact function in AMs remains largely obscure. Using porcine 3D4/21 AM cells as a model, we characterized the transcriptomic and epigenomic alterations after the inhibition of EZH2. We found that the inhibition of EZH2 causes transcriptional activation of numerous immune genes and inhibits the subsequent infection by influenza A virus. Interestingly, specific families of transposable elements, particularly endogenous retrovirus elements (ERVs) and LINEs which belong to retrotransposons, also become derepressed. While some of the derepressed ERV families are pig-specific, a few ancestral families are known to be under EZH2-mediated repression in humans. Given that derepression of ERVs can promote innate immune activation through “viral mimicry”, we speculate that ERVs may also contribute to the coinciding immune activation in AMs after the inhibition of EZH2. Overall, this study improves the understanding of the EZH2-related immune regulation in AMs and provides novel insights into the epigenetic regulation of retrotransposons in pigs. MDPI 2023-01-25 /pmc/articles/PMC9917017/ /pubmed/36768720 http://dx.doi.org/10.3390/ijms24032394 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Liangliang
Jin, Jian
Qin, Weiyun
Jiang, Jing
Bao, Wenbin
Sun, Ming-an
Inhibition of EZH2 Causes Retrotransposon Derepression and Immune Activation in Porcine Lung Alveolar Macrophages
title Inhibition of EZH2 Causes Retrotransposon Derepression and Immune Activation in Porcine Lung Alveolar Macrophages
title_full Inhibition of EZH2 Causes Retrotransposon Derepression and Immune Activation in Porcine Lung Alveolar Macrophages
title_fullStr Inhibition of EZH2 Causes Retrotransposon Derepression and Immune Activation in Porcine Lung Alveolar Macrophages
title_full_unstemmed Inhibition of EZH2 Causes Retrotransposon Derepression and Immune Activation in Porcine Lung Alveolar Macrophages
title_short Inhibition of EZH2 Causes Retrotransposon Derepression and Immune Activation in Porcine Lung Alveolar Macrophages
title_sort inhibition of ezh2 causes retrotransposon derepression and immune activation in porcine lung alveolar macrophages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917017/
https://www.ncbi.nlm.nih.gov/pubmed/36768720
http://dx.doi.org/10.3390/ijms24032394
work_keys_str_mv AT zhangliangliang inhibitionofezh2causesretrotransposonderepressionandimmuneactivationinporcinelungalveolarmacrophages
AT jinjian inhibitionofezh2causesretrotransposonderepressionandimmuneactivationinporcinelungalveolarmacrophages
AT qinweiyun inhibitionofezh2causesretrotransposonderepressionandimmuneactivationinporcinelungalveolarmacrophages
AT jiangjing inhibitionofezh2causesretrotransposonderepressionandimmuneactivationinporcinelungalveolarmacrophages
AT baowenbin inhibitionofezh2causesretrotransposonderepressionandimmuneactivationinporcinelungalveolarmacrophages
AT sunmingan inhibitionofezh2causesretrotransposonderepressionandimmuneactivationinporcinelungalveolarmacrophages