Cargando…
ZNF580 – a brake on Interleukin-6
BACKGROUND: Zinc finger protein 580 (ZNF580) was reported to modulate angiogenesis, endothelial homeostasis and blood pressure control. ZNF580 regulated genes include VEGF-A and IL-8. However, it is unknown if ZNF580 could play a role during inflammation. The aim of this study was to find out if ZNF...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198383/ https://www.ncbi.nlm.nih.gov/pubmed/30386182 http://dx.doi.org/10.1186/s12950-018-0196-5 |
_version_ | 1783364954515046400 |
---|---|
author | Stenzel, Philipp Nagorsen, Kaj Bernd, Jonathan Leppert, Ulrike Zakrzewicz, Andreas Berkholz, Janine |
author_facet | Stenzel, Philipp Nagorsen, Kaj Bernd, Jonathan Leppert, Ulrike Zakrzewicz, Andreas Berkholz, Janine |
author_sort | Stenzel, Philipp |
collection | PubMed |
description | BACKGROUND: Zinc finger protein 580 (ZNF580) was reported to modulate angiogenesis, endothelial homeostasis and blood pressure control. ZNF580 regulated genes include VEGF-A and IL-8. However, it is unknown if ZNF580 could play a role during inflammation. The aim of this study was to find out if ZNF580 affects the expression of IL-6, if it occurs in monocytic cells and responds to inflammatory mediators. RESULTS: Overexpression of ZNF580 reduced LPS-induced promotor activity of IL-6. Consistently, overexpression of ZNF580 reduced by half the LPS-induced expression of IL-6. ZNF580 was strongly expressed in the nucleus of MonoMac6, a human monocytic cell line. LPS-stimulated IL-6 secretion increased when ZNF580 was suppressed with siRNA. After stimulation of MonoMac6 with LPS for 24 h, ZNF580 negatively correlated with the amount of secreted IL-6. In response to LPS, ZNF580 was increased within the first 8 h, followed by a marked decrease after 16 h. This decrease coincided with sustained IL-6 production. CONCLUSION: This study demonstrated that ZNF580 inhibits LPS-induced expression of IL-6. ZNF580 was highly expressed in monocytic cells and therefore may contribute to the modulation of its IL-6 production, at least in response to LPS. This suggests cooperation between ZNF580 and NFκB, which could play a role during sepsis. |
format | Online Article Text |
id | pubmed-6198383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61983832018-10-31 ZNF580 – a brake on Interleukin-6 Stenzel, Philipp Nagorsen, Kaj Bernd, Jonathan Leppert, Ulrike Zakrzewicz, Andreas Berkholz, Janine J Inflamm (Lond) Research BACKGROUND: Zinc finger protein 580 (ZNF580) was reported to modulate angiogenesis, endothelial homeostasis and blood pressure control. ZNF580 regulated genes include VEGF-A and IL-8. However, it is unknown if ZNF580 could play a role during inflammation. The aim of this study was to find out if ZNF580 affects the expression of IL-6, if it occurs in monocytic cells and responds to inflammatory mediators. RESULTS: Overexpression of ZNF580 reduced LPS-induced promotor activity of IL-6. Consistently, overexpression of ZNF580 reduced by half the LPS-induced expression of IL-6. ZNF580 was strongly expressed in the nucleus of MonoMac6, a human monocytic cell line. LPS-stimulated IL-6 secretion increased when ZNF580 was suppressed with siRNA. After stimulation of MonoMac6 with LPS for 24 h, ZNF580 negatively correlated with the amount of secreted IL-6. In response to LPS, ZNF580 was increased within the first 8 h, followed by a marked decrease after 16 h. This decrease coincided with sustained IL-6 production. CONCLUSION: This study demonstrated that ZNF580 inhibits LPS-induced expression of IL-6. ZNF580 was highly expressed in monocytic cells and therefore may contribute to the modulation of its IL-6 production, at least in response to LPS. This suggests cooperation between ZNF580 and NFκB, which could play a role during sepsis. BioMed Central 2018-10-22 /pmc/articles/PMC6198383/ /pubmed/30386182 http://dx.doi.org/10.1186/s12950-018-0196-5 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 Stenzel, Philipp Nagorsen, Kaj Bernd, Jonathan Leppert, Ulrike Zakrzewicz, Andreas Berkholz, Janine ZNF580 – a brake on Interleukin-6 |
title | ZNF580 – a brake on Interleukin-6 |
title_full | ZNF580 – a brake on Interleukin-6 |
title_fullStr | ZNF580 – a brake on Interleukin-6 |
title_full_unstemmed | ZNF580 – a brake on Interleukin-6 |
title_short | ZNF580 – a brake on Interleukin-6 |
title_sort | znf580 – a brake on interleukin-6 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198383/ https://www.ncbi.nlm.nih.gov/pubmed/30386182 http://dx.doi.org/10.1186/s12950-018-0196-5 |
work_keys_str_mv | AT stenzelphilipp znf580abrakeoninterleukin6 AT nagorsenkaj znf580abrakeoninterleukin6 AT berndjonathan znf580abrakeoninterleukin6 AT leppertulrike znf580abrakeoninterleukin6 AT zakrzewiczandreas znf580abrakeoninterleukin6 AT berkholzjanine znf580abrakeoninterleukin6 |