Cargando…
Inducible MicroRNA-223 Down-Regulation Promotes TLR-Triggered IL-6 and IL-1β Production in Macrophages by Targeting STAT3
MicroRNAs are small non-coding RNA molecules that regulate gene expression by either translational inhibition or mRNA degradation. MicroRNAs play pivotal roles in the regulation of both innate and adaptive immune responses, including TLR-triggered inflammatory response. Here we reported that the exp...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3427313/ https://www.ncbi.nlm.nih.gov/pubmed/22937006 http://dx.doi.org/10.1371/journal.pone.0042971 |
_version_ | 1782241597866377216 |
---|---|
author | Chen, Qingyun Wang, Hui Liu, Yang Song, Yinjing Lai, Lihua Han, Quan Cao, Xuetao Wang, Qingqing |
author_facet | Chen, Qingyun Wang, Hui Liu, Yang Song, Yinjing Lai, Lihua Han, Quan Cao, Xuetao Wang, Qingqing |
author_sort | Chen, Qingyun |
collection | PubMed |
description | MicroRNAs are small non-coding RNA molecules that regulate gene expression by either translational inhibition or mRNA degradation. MicroRNAs play pivotal roles in the regulation of both innate and adaptive immune responses, including TLR-triggered inflammatory response. Here we reported that the expression of microRNA-223 (miR-223) was significantly decreased in murine macrophages during activation by lipopolysaccharide (LPS) or poly (I∶C) stimulation. The inducible miR-223 down-regulation resulted in the activation of signal transducer and activator of transcription 3 (STAT3), which is directly targeted by miR-223, thus promoting the production of pro-inflammatory cytokines IL-6 and IL-1β, but not TNF-α. Interestingly, IL-6 was found to be a main factor in inducing the decrease in miR-223 expression after LPS stimulation, which formed a positive feedback loop to regulate IL-6 and IL-1β. Herein, our findings provide a new explanation characterizing the molecular mechanism responsible for the regulation of IL-6 production after TLR-triggered macrophage activation. |
format | Online Article Text |
id | pubmed-3427313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34273132012-08-30 Inducible MicroRNA-223 Down-Regulation Promotes TLR-Triggered IL-6 and IL-1β Production in Macrophages by Targeting STAT3 Chen, Qingyun Wang, Hui Liu, Yang Song, Yinjing Lai, Lihua Han, Quan Cao, Xuetao Wang, Qingqing PLoS One Research Article MicroRNAs are small non-coding RNA molecules that regulate gene expression by either translational inhibition or mRNA degradation. MicroRNAs play pivotal roles in the regulation of both innate and adaptive immune responses, including TLR-triggered inflammatory response. Here we reported that the expression of microRNA-223 (miR-223) was significantly decreased in murine macrophages during activation by lipopolysaccharide (LPS) or poly (I∶C) stimulation. The inducible miR-223 down-regulation resulted in the activation of signal transducer and activator of transcription 3 (STAT3), which is directly targeted by miR-223, thus promoting the production of pro-inflammatory cytokines IL-6 and IL-1β, but not TNF-α. Interestingly, IL-6 was found to be a main factor in inducing the decrease in miR-223 expression after LPS stimulation, which formed a positive feedback loop to regulate IL-6 and IL-1β. Herein, our findings provide a new explanation characterizing the molecular mechanism responsible for the regulation of IL-6 production after TLR-triggered macrophage activation. Public Library of Science 2012-08-24 /pmc/articles/PMC3427313/ /pubmed/22937006 http://dx.doi.org/10.1371/journal.pone.0042971 Text en © 2012 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chen, Qingyun Wang, Hui Liu, Yang Song, Yinjing Lai, Lihua Han, Quan Cao, Xuetao Wang, Qingqing Inducible MicroRNA-223 Down-Regulation Promotes TLR-Triggered IL-6 and IL-1β Production in Macrophages by Targeting STAT3 |
title | Inducible MicroRNA-223 Down-Regulation Promotes TLR-Triggered IL-6 and IL-1β Production in Macrophages by Targeting STAT3 |
title_full | Inducible MicroRNA-223 Down-Regulation Promotes TLR-Triggered IL-6 and IL-1β Production in Macrophages by Targeting STAT3 |
title_fullStr | Inducible MicroRNA-223 Down-Regulation Promotes TLR-Triggered IL-6 and IL-1β Production in Macrophages by Targeting STAT3 |
title_full_unstemmed | Inducible MicroRNA-223 Down-Regulation Promotes TLR-Triggered IL-6 and IL-1β Production in Macrophages by Targeting STAT3 |
title_short | Inducible MicroRNA-223 Down-Regulation Promotes TLR-Triggered IL-6 and IL-1β Production in Macrophages by Targeting STAT3 |
title_sort | inducible microrna-223 down-regulation promotes tlr-triggered il-6 and il-1β production in macrophages by targeting stat3 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3427313/ https://www.ncbi.nlm.nih.gov/pubmed/22937006 http://dx.doi.org/10.1371/journal.pone.0042971 |
work_keys_str_mv | AT chenqingyun induciblemicrorna223downregulationpromotestlrtriggeredil6andil1bproductioninmacrophagesbytargetingstat3 AT wanghui induciblemicrorna223downregulationpromotestlrtriggeredil6andil1bproductioninmacrophagesbytargetingstat3 AT liuyang induciblemicrorna223downregulationpromotestlrtriggeredil6andil1bproductioninmacrophagesbytargetingstat3 AT songyinjing induciblemicrorna223downregulationpromotestlrtriggeredil6andil1bproductioninmacrophagesbytargetingstat3 AT lailihua induciblemicrorna223downregulationpromotestlrtriggeredil6andil1bproductioninmacrophagesbytargetingstat3 AT hanquan induciblemicrorna223downregulationpromotestlrtriggeredil6andil1bproductioninmacrophagesbytargetingstat3 AT caoxuetao induciblemicrorna223downregulationpromotestlrtriggeredil6andil1bproductioninmacrophagesbytargetingstat3 AT wangqingqing induciblemicrorna223downregulationpromotestlrtriggeredil6andil1bproductioninmacrophagesbytargetingstat3 |