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Tribbles-2 is a novel regulator of inflammatory activation of monocytes
Inflammatory activation of monocytes is an essential part of both innate immune responses and the pathogenesis of conditions such as atherosclerosis. However, the mechanisms which modulate the response of monocytes to inflammatory stimuli are still poorly understood. Here, we report that tribbles-2...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638877/ https://www.ncbi.nlm.nih.gov/pubmed/18952906 http://dx.doi.org/10.1093/intimm/dxn116 |
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author | Eder, Katalin Guan, Hongtao Sung, Hye Y. Ward, Jon Angyal, Adrienn Janas, Michelle Sarmay, Gabriella Duda, Erno Turner, Martin Dower, Steven K. Francis, Sheila E. Crossman, David C. Kiss-Toth, Endre |
author_facet | Eder, Katalin Guan, Hongtao Sung, Hye Y. Ward, Jon Angyal, Adrienn Janas, Michelle Sarmay, Gabriella Duda, Erno Turner, Martin Dower, Steven K. Francis, Sheila E. Crossman, David C. Kiss-Toth, Endre |
author_sort | Eder, Katalin |
collection | PubMed |
description | Inflammatory activation of monocytes is an essential part of both innate immune responses and the pathogenesis of conditions such as atherosclerosis. However, the mechanisms which modulate the response of monocytes to inflammatory stimuli are still poorly understood. Here, we report that tribbles-2 (trb-2) is a novel regulator of inflammatory activation of monocytes. Down-regulation of trb-2 levels potentiates LPS-induced IL-8 production via enhanced activation of the extracellular signal-regulated kinase and jun kinase mitogen-activated protein kinase (MAPK) pathways. In keeping with this, the endogenous level of trb-2 expression in human primary monocytes is inversely correlated to the cell’s ability to produce IL-8. We show that trb-2 is a binding partner and a negative regulator of selected MAPKs. The potential in vivo relevance of these findings is highlighted by the observation that modified low-density lipoprotein profoundly down-regulates trb-2 expression, which may, in turn, significantly contribute to the inflammatory processes in the development of vascular disease. Taken together, our results define trb-2 as a potent novel regulator of monocyte biology, controlling the activation of these cells. |
format | Text |
id | pubmed-2638877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26388772009-02-25 Tribbles-2 is a novel regulator of inflammatory activation of monocytes Eder, Katalin Guan, Hongtao Sung, Hye Y. Ward, Jon Angyal, Adrienn Janas, Michelle Sarmay, Gabriella Duda, Erno Turner, Martin Dower, Steven K. Francis, Sheila E. Crossman, David C. Kiss-Toth, Endre Int Immunol Featured Article of the Month Inflammatory activation of monocytes is an essential part of both innate immune responses and the pathogenesis of conditions such as atherosclerosis. However, the mechanisms which modulate the response of monocytes to inflammatory stimuli are still poorly understood. Here, we report that tribbles-2 (trb-2) is a novel regulator of inflammatory activation of monocytes. Down-regulation of trb-2 levels potentiates LPS-induced IL-8 production via enhanced activation of the extracellular signal-regulated kinase and jun kinase mitogen-activated protein kinase (MAPK) pathways. In keeping with this, the endogenous level of trb-2 expression in human primary monocytes is inversely correlated to the cell’s ability to produce IL-8. We show that trb-2 is a binding partner and a negative regulator of selected MAPKs. The potential in vivo relevance of these findings is highlighted by the observation that modified low-density lipoprotein profoundly down-regulates trb-2 expression, which may, in turn, significantly contribute to the inflammatory processes in the development of vascular disease. Taken together, our results define trb-2 as a potent novel regulator of monocyte biology, controlling the activation of these cells. Oxford University Press 2008-12 2008-10-24 /pmc/articles/PMC2638877/ /pubmed/18952906 http://dx.doi.org/10.1093/intimm/dxn116 Text en © The Author 2008. Published by Oxford University Press on behalf of The Japanese Society for Immunology. All rights reserved. The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press and The Japanese Society for Immunology are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org |
spellingShingle | Featured Article of the Month Eder, Katalin Guan, Hongtao Sung, Hye Y. Ward, Jon Angyal, Adrienn Janas, Michelle Sarmay, Gabriella Duda, Erno Turner, Martin Dower, Steven K. Francis, Sheila E. Crossman, David C. Kiss-Toth, Endre Tribbles-2 is a novel regulator of inflammatory activation of monocytes |
title | Tribbles-2 is a novel regulator of inflammatory activation of monocytes |
title_full | Tribbles-2 is a novel regulator of inflammatory activation of monocytes |
title_fullStr | Tribbles-2 is a novel regulator of inflammatory activation of monocytes |
title_full_unstemmed | Tribbles-2 is a novel regulator of inflammatory activation of monocytes |
title_short | Tribbles-2 is a novel regulator of inflammatory activation of monocytes |
title_sort | tribbles-2 is a novel regulator of inflammatory activation of monocytes |
topic | Featured Article of the Month |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638877/ https://www.ncbi.nlm.nih.gov/pubmed/18952906 http://dx.doi.org/10.1093/intimm/dxn116 |
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