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miR-346 Controls Release of TNF-α Protein and Stability of Its mRNA in Rheumatoid Arthritis via Tristetraprolin Stabilization

TNF-α is a major cytokine implicated in rheumatoid arthritis. Its expression is regulated both at the transcriptional and posttranscriptional levels and recent data demonstrated that miRNAs are implicated in TNF-α response in macrophages. LPS-activated FLS isolated from RA patients express TNF-α mRN...

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Autores principales: Semaan, Noha, Frenzel, Laurent, Alsaleh, Ghada, Suffert, Guillaume, Gottenberg, Jacques-Eric, Sibilia, Jean, Pfeffer, Sebastien, Wachsmann, Dominique
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096642/
https://www.ncbi.nlm.nih.gov/pubmed/21611196
http://dx.doi.org/10.1371/journal.pone.0019827
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author Semaan, Noha
Frenzel, Laurent
Alsaleh, Ghada
Suffert, Guillaume
Gottenberg, Jacques-Eric
Sibilia, Jean
Pfeffer, Sebastien
Wachsmann, Dominique
author_facet Semaan, Noha
Frenzel, Laurent
Alsaleh, Ghada
Suffert, Guillaume
Gottenberg, Jacques-Eric
Sibilia, Jean
Pfeffer, Sebastien
Wachsmann, Dominique
author_sort Semaan, Noha
collection PubMed
description TNF-α is a major cytokine implicated in rheumatoid arthritis. Its expression is regulated both at the transcriptional and posttranscriptional levels and recent data demonstrated that miRNAs are implicated in TNF-α response in macrophages. LPS-activated FLS isolated from RA patients express TNF-α mRNA but not the mature protein. This prompted us to look for miRNAs which could be implicated in this anti-inflammatory effect. Using a microarray, we found two miRNAs, miR-125b and miR-939 predicted to target the 3′-UTR of TNF-α mRNA, to be up-regulated in RA FLS in response to LPS, but their repression did not restore mature TNF-α expression in FLS. We showed previously that miR-346, which is upregulated in LPS-activated FLS, inhibited Btk expression that stabilized TNF-α mRNA. Blocking miR-346 reestablished TNF-α expression in activated FLS. Interestingly, transfection of miR-346 in LPS-activated THP-1 cells inhibited TNF-α secretion. We also demonstrated that TTP, a RNA binding protein which inhibited TNF-α synthesis, is overexpressed in activated FLS and that inhibition of miR-346 decreases its expression. Conversely, transfection of miR-346 in LPS-activated THP-1 cells increased TTP mRNA expression and inhibited TNF-α release. These results indicate that miR-346 controls TNF-α synthesis by regulating TTP expression.
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spelling pubmed-30966422011-05-24 miR-346 Controls Release of TNF-α Protein and Stability of Its mRNA in Rheumatoid Arthritis via Tristetraprolin Stabilization Semaan, Noha Frenzel, Laurent Alsaleh, Ghada Suffert, Guillaume Gottenberg, Jacques-Eric Sibilia, Jean Pfeffer, Sebastien Wachsmann, Dominique PLoS One Research Article TNF-α is a major cytokine implicated in rheumatoid arthritis. Its expression is regulated both at the transcriptional and posttranscriptional levels and recent data demonstrated that miRNAs are implicated in TNF-α response in macrophages. LPS-activated FLS isolated from RA patients express TNF-α mRNA but not the mature protein. This prompted us to look for miRNAs which could be implicated in this anti-inflammatory effect. Using a microarray, we found two miRNAs, miR-125b and miR-939 predicted to target the 3′-UTR of TNF-α mRNA, to be up-regulated in RA FLS in response to LPS, but their repression did not restore mature TNF-α expression in FLS. We showed previously that miR-346, which is upregulated in LPS-activated FLS, inhibited Btk expression that stabilized TNF-α mRNA. Blocking miR-346 reestablished TNF-α expression in activated FLS. Interestingly, transfection of miR-346 in LPS-activated THP-1 cells inhibited TNF-α secretion. We also demonstrated that TTP, a RNA binding protein which inhibited TNF-α synthesis, is overexpressed in activated FLS and that inhibition of miR-346 decreases its expression. Conversely, transfection of miR-346 in LPS-activated THP-1 cells increased TTP mRNA expression and inhibited TNF-α release. These results indicate that miR-346 controls TNF-α synthesis by regulating TTP expression. Public Library of Science 2011-05-17 /pmc/articles/PMC3096642/ /pubmed/21611196 http://dx.doi.org/10.1371/journal.pone.0019827 Text en Semaan 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
Semaan, Noha
Frenzel, Laurent
Alsaleh, Ghada
Suffert, Guillaume
Gottenberg, Jacques-Eric
Sibilia, Jean
Pfeffer, Sebastien
Wachsmann, Dominique
miR-346 Controls Release of TNF-α Protein and Stability of Its mRNA in Rheumatoid Arthritis via Tristetraprolin Stabilization
title miR-346 Controls Release of TNF-α Protein and Stability of Its mRNA in Rheumatoid Arthritis via Tristetraprolin Stabilization
title_full miR-346 Controls Release of TNF-α Protein and Stability of Its mRNA in Rheumatoid Arthritis via Tristetraprolin Stabilization
title_fullStr miR-346 Controls Release of TNF-α Protein and Stability of Its mRNA in Rheumatoid Arthritis via Tristetraprolin Stabilization
title_full_unstemmed miR-346 Controls Release of TNF-α Protein and Stability of Its mRNA in Rheumatoid Arthritis via Tristetraprolin Stabilization
title_short miR-346 Controls Release of TNF-α Protein and Stability of Its mRNA in Rheumatoid Arthritis via Tristetraprolin Stabilization
title_sort mir-346 controls release of tnf-α protein and stability of its mrna in rheumatoid arthritis via tristetraprolin stabilization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096642/
https://www.ncbi.nlm.nih.gov/pubmed/21611196
http://dx.doi.org/10.1371/journal.pone.0019827
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