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N6-Methyladenosine (m6A) Modification in Natural Immune Cell-Mediated Inflammatory Diseases
The post-transcriptional N6-methyladenosine (m6A) modification of RNA influences stability, transport, and translation with implications for various physiological and pathological processes. Immune cell development, differentiation, and activation are also thought to be regulated by m6A and affect h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673353/ https://www.ncbi.nlm.nih.gov/pubmed/37903470 http://dx.doi.org/10.1159/000534162 |
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author | Teng, Yan Yi, Jin Chen, Junnian Yang, Lu |
author_facet | Teng, Yan Yi, Jin Chen, Junnian Yang, Lu |
author_sort | Teng, Yan |
collection | PubMed |
description | The post-transcriptional N6-methyladenosine (m6A) modification of RNA influences stability, transport, and translation with implications for various physiological and pathological processes. Immune cell development, differentiation, and activation are also thought to be regulated by m6A and affect host defense against pathogens and inflammatory response with impacts on infectious, neoplastic, autoimmune, cardiovascular, hepatic, and osteal diseases. The current review summarizes recent research on m6A in monocyte/macrophages, neutrophils, dendritic cells, natural killer cells, and microglia and gives insights into epigenetic modifications of the immune system and novel therapeutic strategies for immune-related diseases. |
format | Online Article Text |
id | pubmed-10673353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-106733532023-10-30 N6-Methyladenosine (m6A) Modification in Natural Immune Cell-Mediated Inflammatory Diseases Teng, Yan Yi, Jin Chen, Junnian Yang, Lu J Innate Immun Review Article The post-transcriptional N6-methyladenosine (m6A) modification of RNA influences stability, transport, and translation with implications for various physiological and pathological processes. Immune cell development, differentiation, and activation are also thought to be regulated by m6A and affect host defense against pathogens and inflammatory response with impacts on infectious, neoplastic, autoimmune, cardiovascular, hepatic, and osteal diseases. The current review summarizes recent research on m6A in monocyte/macrophages, neutrophils, dendritic cells, natural killer cells, and microglia and gives insights into epigenetic modifications of the immune system and novel therapeutic strategies for immune-related diseases. S. Karger AG 2023-10-30 /pmc/articles/PMC10673353/ /pubmed/37903470 http://dx.doi.org/10.1159/000534162 Text en © 2023 The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Review Article Teng, Yan Yi, Jin Chen, Junnian Yang, Lu N6-Methyladenosine (m6A) Modification in Natural Immune Cell-Mediated Inflammatory Diseases |
title | N6-Methyladenosine (m6A) Modification in Natural Immune Cell-Mediated Inflammatory Diseases |
title_full | N6-Methyladenosine (m6A) Modification in Natural Immune Cell-Mediated Inflammatory Diseases |
title_fullStr | N6-Methyladenosine (m6A) Modification in Natural Immune Cell-Mediated Inflammatory Diseases |
title_full_unstemmed | N6-Methyladenosine (m6A) Modification in Natural Immune Cell-Mediated Inflammatory Diseases |
title_short | N6-Methyladenosine (m6A) Modification in Natural Immune Cell-Mediated Inflammatory Diseases |
title_sort | n6-methyladenosine (m6a) modification in natural immune cell-mediated inflammatory diseases |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673353/ https://www.ncbi.nlm.nih.gov/pubmed/37903470 http://dx.doi.org/10.1159/000534162 |
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