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PTPIP51—A New RelA-tionship with the NFκB Signaling Pathway
The present study shows a new connection of protein tyrosine phosphatase interacting protein 51 (PTPIP51) to the nuclear factor κB (NFκB) signalling pathway. PTPIP51 mRNA and protein expression is regulated by RelA. If bound to the PTPIP51 promoter, RelA repress the mRNA and protein expression of PT...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496682/ https://www.ncbi.nlm.nih.gov/pubmed/25893721 http://dx.doi.org/10.3390/biom5020485 |
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author | Brobeil, Alexander Kämmerer, Fabian Tag, Claudia Steger, Klaus Gattenlöhner, Stefan Wimmer, Monika |
author_facet | Brobeil, Alexander Kämmerer, Fabian Tag, Claudia Steger, Klaus Gattenlöhner, Stefan Wimmer, Monika |
author_sort | Brobeil, Alexander |
collection | PubMed |
description | The present study shows a new connection of protein tyrosine phosphatase interacting protein 51 (PTPIP51) to the nuclear factor κB (NFκB) signalling pathway. PTPIP51 mRNA and protein expression is regulated by RelA. If bound to the PTPIP51 promoter, RelA repress the mRNA and protein expression of PTPIP51. The parallel treatment with pyrrolidine dithiocarbamate (PDTC) reversed the suppression of PTPIP51 protein expression induced by TNFα. Using the intensity correlation analysis PTPIP51 verified a co-localization with RelA, which is also regulated by TNFα administration. Moreover, the direct interaction of PTPIP51 and RelA was established using the DuoLink proximity ligation assay. IκBα, the known inhibitor of RelA, also interacted with PTPIP51. This hints to the fact that in un-stimulated conditions PTPIP51 forms a complex with RelA and IκBα. The PTPIP51/RelA/IκBα complex is modulated by TNFα. Interestingly, the impact on the mitogen activated protein kinase pathway was negligible except in highest TNFα concentration. Here, PTPIP51 and Raf-1 interactions were slightly repressed. The newly established relationship of PTPIP51 and the NFκB signaling pathway provides the basis for a possible therapeutic impact. |
format | Online Article Text |
id | pubmed-4496682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44966822015-07-10 PTPIP51—A New RelA-tionship with the NFκB Signaling Pathway Brobeil, Alexander Kämmerer, Fabian Tag, Claudia Steger, Klaus Gattenlöhner, Stefan Wimmer, Monika Biomolecules Article The present study shows a new connection of protein tyrosine phosphatase interacting protein 51 (PTPIP51) to the nuclear factor κB (NFκB) signalling pathway. PTPIP51 mRNA and protein expression is regulated by RelA. If bound to the PTPIP51 promoter, RelA repress the mRNA and protein expression of PTPIP51. The parallel treatment with pyrrolidine dithiocarbamate (PDTC) reversed the suppression of PTPIP51 protein expression induced by TNFα. Using the intensity correlation analysis PTPIP51 verified a co-localization with RelA, which is also regulated by TNFα administration. Moreover, the direct interaction of PTPIP51 and RelA was established using the DuoLink proximity ligation assay. IκBα, the known inhibitor of RelA, also interacted with PTPIP51. This hints to the fact that in un-stimulated conditions PTPIP51 forms a complex with RelA and IκBα. The PTPIP51/RelA/IκBα complex is modulated by TNFα. Interestingly, the impact on the mitogen activated protein kinase pathway was negligible except in highest TNFα concentration. Here, PTPIP51 and Raf-1 interactions were slightly repressed. The newly established relationship of PTPIP51 and the NFκB signaling pathway provides the basis for a possible therapeutic impact. MDPI 2015-04-16 /pmc/articles/PMC4496682/ /pubmed/25893721 http://dx.doi.org/10.3390/biom5020485 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Brobeil, Alexander Kämmerer, Fabian Tag, Claudia Steger, Klaus Gattenlöhner, Stefan Wimmer, Monika PTPIP51—A New RelA-tionship with the NFκB Signaling Pathway |
title | PTPIP51—A New RelA-tionship with the NFκB Signaling Pathway |
title_full | PTPIP51—A New RelA-tionship with the NFκB Signaling Pathway |
title_fullStr | PTPIP51—A New RelA-tionship with the NFκB Signaling Pathway |
title_full_unstemmed | PTPIP51—A New RelA-tionship with the NFκB Signaling Pathway |
title_short | PTPIP51—A New RelA-tionship with the NFκB Signaling Pathway |
title_sort | ptpip51—a new rela-tionship with the nfκb signaling pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496682/ https://www.ncbi.nlm.nih.gov/pubmed/25893721 http://dx.doi.org/10.3390/biom5020485 |
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