Down-Regulation of Tristetraprolin Expression Results in Enhanced IL-12 and MIP-2 Production and Reduced MIP-3α Synthesis in Activated Macrophages

In inflammation, the post-transcriptional regulation of transiently expressed genes provides a potential therapeutic target. Tristetraprolin (TTP) is of the factors regulating decay of cytokine mRNAs. The aim of the present study was to identify cytokines whose expression is regulated by TTP. We est...

Full description

Saved in:
Bibliographic Details
Main Authors: Ulla Jalonen, Riina Nieminen, Katriina Vuolteenaho, Hannu Kankaanranta, Eeva Moilanen
Format: Article
Language:English
Published: Wiley 2006-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/MI/2006/40691
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832550071279812608
author Ulla Jalonen
Riina Nieminen
Katriina Vuolteenaho
Hannu Kankaanranta
Eeva Moilanen
author_facet Ulla Jalonen
Riina Nieminen
Katriina Vuolteenaho
Hannu Kankaanranta
Eeva Moilanen
author_sort Ulla Jalonen
collection DOAJ
description In inflammation, the post-transcriptional regulation of transiently expressed genes provides a potential therapeutic target. Tristetraprolin (TTP) is of the factors regulating decay of cytokine mRNAs. The aim of the present study was to identify cytokines whose expression is regulated by TTP. We established a TTP knock-down cell line by expressing shRNA against TTP (shTTP cell line). A cytokine antibody array was used to measure cytokine production in macrophages exposed to lipopolysaccharide (LPS). Cytokines IL-6, IL-12, TNF-α, and MIP-2 (a homologue to human IL-8) were expressed at higher levels whereas MIP-3α was produced at lower levels in LPS-treated shTTP cells than in control cells suggesting that the expression of these cytokines is regulated by TTP. The present data provide IL-12, MIP-2, and MIP-3α as novel inflammatory cytokine targets for TTP-mediated mRNA decay and stress the role of TTP in the regulation of the inflammatory process.
format Article
id doaj-art-65fb0657e4ad4255afa4a6e7b727b4d9
institution Kabale University
issn 0962-9351
1466-1861
language English
publishDate 2006-01-01
publisher Wiley
record_format Article
series Mediators of Inflammation
spelling doaj-art-65fb0657e4ad4255afa4a6e7b727b4d92025-02-03T06:07:48ZengWileyMediators of Inflammation0962-93511466-18612006-01-01200610.1155/MI/2006/4069140691Down-Regulation of Tristetraprolin Expression Results in Enhanced IL-12 and MIP-2 Production and Reduced MIP-3α Synthesis in Activated MacrophagesUlla Jalonen0Riina Nieminen1Katriina Vuolteenaho2Hannu Kankaanranta3Eeva Moilanen4The Immunopharmacology Research Group, Medical School, University of Tampere, and Tampere University Hospital, Research Unit, Tampere 33014, FinlandThe Immunopharmacology Research Group, Medical School, University of Tampere, and Tampere University Hospital, Research Unit, Tampere 33014, FinlandThe Immunopharmacology Research Group, Medical School, University of Tampere, and Tampere University Hospital, Research Unit, Tampere 33014, FinlandThe Immunopharmacology Research Group, Medical School, University of Tampere, and Tampere University Hospital, Research Unit, Tampere 33014, FinlandThe Immunopharmacology Research Group, Medical School, University of Tampere, and Tampere University Hospital, Research Unit, Tampere 33014, FinlandIn inflammation, the post-transcriptional regulation of transiently expressed genes provides a potential therapeutic target. Tristetraprolin (TTP) is of the factors regulating decay of cytokine mRNAs. The aim of the present study was to identify cytokines whose expression is regulated by TTP. We established a TTP knock-down cell line by expressing shRNA against TTP (shTTP cell line). A cytokine antibody array was used to measure cytokine production in macrophages exposed to lipopolysaccharide (LPS). Cytokines IL-6, IL-12, TNF-α, and MIP-2 (a homologue to human IL-8) were expressed at higher levels whereas MIP-3α was produced at lower levels in LPS-treated shTTP cells than in control cells suggesting that the expression of these cytokines is regulated by TTP. The present data provide IL-12, MIP-2, and MIP-3α as novel inflammatory cytokine targets for TTP-mediated mRNA decay and stress the role of TTP in the regulation of the inflammatory process.http://dx.doi.org/10.1155/MI/2006/40691
spellingShingle Ulla Jalonen
Riina Nieminen
Katriina Vuolteenaho
Hannu Kankaanranta
Eeva Moilanen
Down-Regulation of Tristetraprolin Expression Results in Enhanced IL-12 and MIP-2 Production and Reduced MIP-3α Synthesis in Activated Macrophages
Mediators of Inflammation
title Down-Regulation of Tristetraprolin Expression Results in Enhanced IL-12 and MIP-2 Production and Reduced MIP-3α Synthesis in Activated Macrophages
title_full Down-Regulation of Tristetraprolin Expression Results in Enhanced IL-12 and MIP-2 Production and Reduced MIP-3α Synthesis in Activated Macrophages
title_fullStr Down-Regulation of Tristetraprolin Expression Results in Enhanced IL-12 and MIP-2 Production and Reduced MIP-3α Synthesis in Activated Macrophages
title_full_unstemmed Down-Regulation of Tristetraprolin Expression Results in Enhanced IL-12 and MIP-2 Production and Reduced MIP-3α Synthesis in Activated Macrophages
title_short Down-Regulation of Tristetraprolin Expression Results in Enhanced IL-12 and MIP-2 Production and Reduced MIP-3α Synthesis in Activated Macrophages
title_sort down regulation of tristetraprolin expression results in enhanced il 12 and mip 2 production and reduced mip 3α synthesis in activated macrophages
url http://dx.doi.org/10.1155/MI/2006/40691
work_keys_str_mv AT ullajalonen downregulationoftristetraprolinexpressionresultsinenhancedil12andmip2productionandreducedmip3asynthesisinactivatedmacrophages
AT riinanieminen downregulationoftristetraprolinexpressionresultsinenhancedil12andmip2productionandreducedmip3asynthesisinactivatedmacrophages
AT katriinavuolteenaho downregulationoftristetraprolinexpressionresultsinenhancedil12andmip2productionandreducedmip3asynthesisinactivatedmacrophages
AT hannukankaanranta downregulationoftristetraprolinexpressionresultsinenhancedil12andmip2productionandreducedmip3asynthesisinactivatedmacrophages
AT eevamoilanen downregulationoftristetraprolinexpressionresultsinenhancedil12andmip2productionandreducedmip3asynthesisinactivatedmacrophages