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Rho protein GTPases and their interactions with NFκB: crossroads of inflammation and matrix biology
The RhoGTPases, with RhoA, Cdc42 and Rac being major members, are a group of key ubiquitous proteins present in all eukaryotic organisms that subserve such important functions as cell migration, adhesion and differentiation. The NFκB (nuclear factor κB) is a family of constitutive and inducible tran...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069681/ https://www.ncbi.nlm.nih.gov/pubmed/24877606 http://dx.doi.org/10.1042/BSR20140021 |
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author | Tong, Louis Tergaonkar, Vinay |
author_facet | Tong, Louis Tergaonkar, Vinay |
author_sort | Tong, Louis |
collection | PubMed |
description | The RhoGTPases, with RhoA, Cdc42 and Rac being major members, are a group of key ubiquitous proteins present in all eukaryotic organisms that subserve such important functions as cell migration, adhesion and differentiation. The NFκB (nuclear factor κB) is a family of constitutive and inducible transcription factors that through their diverse target genes, play a major role in processes such as cytokine expression, stress regulation, cell division and transformation. Research over the past decade has uncovered new molecular links between the RhoGTPases and the NFκB pathway, with the RhoGTPases playing a positive or negative regulatory role on NFκB activation depending on the context. The RhoA–NFκB interaction has been shown to be important in cytokine-activated NFκB processes, such as those induced by TNFα (tumour necrosis factor α). On the other hand, Rac is important for activating the NFκB response downstream of integrin activation, such as after phagocytosis. Specific residues of Rac1 are important for triggering NFκB activation, and mutations do obliterate this response. Other upstream triggers of the RhoGTPase–NFκB interactions include the suppressive p120 catenin, with implications for skin inflammation. The networks described here are not only important areas for further research, but are also significant for discovery of targets for translational medicine. |
format | Online Article Text |
id | pubmed-4069681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40696812014-06-25 Rho protein GTPases and their interactions with NFκB: crossroads of inflammation and matrix biology Tong, Louis Tergaonkar, Vinay Biosci Rep Review Article The RhoGTPases, with RhoA, Cdc42 and Rac being major members, are a group of key ubiquitous proteins present in all eukaryotic organisms that subserve such important functions as cell migration, adhesion and differentiation. The NFκB (nuclear factor κB) is a family of constitutive and inducible transcription factors that through their diverse target genes, play a major role in processes such as cytokine expression, stress regulation, cell division and transformation. Research over the past decade has uncovered new molecular links between the RhoGTPases and the NFκB pathway, with the RhoGTPases playing a positive or negative regulatory role on NFκB activation depending on the context. The RhoA–NFκB interaction has been shown to be important in cytokine-activated NFκB processes, such as those induced by TNFα (tumour necrosis factor α). On the other hand, Rac is important for activating the NFκB response downstream of integrin activation, such as after phagocytosis. Specific residues of Rac1 are important for triggering NFκB activation, and mutations do obliterate this response. Other upstream triggers of the RhoGTPase–NFκB interactions include the suppressive p120 catenin, with implications for skin inflammation. The networks described here are not only important areas for further research, but are also significant for discovery of targets for translational medicine. Portland Press Ltd. 2014-06-25 /pmc/articles/PMC4069681/ /pubmed/24877606 http://dx.doi.org/10.1042/BSR20140021 Text en © 2014 The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Licence (CC-BY)(http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Tong, Louis Tergaonkar, Vinay Rho protein GTPases and their interactions with NFκB: crossroads of inflammation and matrix biology |
title | Rho protein GTPases and their interactions with NFκB: crossroads of inflammation and matrix biology |
title_full | Rho protein GTPases and their interactions with NFκB: crossroads of inflammation and matrix biology |
title_fullStr | Rho protein GTPases and their interactions with NFκB: crossroads of inflammation and matrix biology |
title_full_unstemmed | Rho protein GTPases and their interactions with NFκB: crossroads of inflammation and matrix biology |
title_short | Rho protein GTPases and their interactions with NFκB: crossroads of inflammation and matrix biology |
title_sort | rho protein gtpases and their interactions with nfκb: crossroads of inflammation and matrix biology |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069681/ https://www.ncbi.nlm.nih.gov/pubmed/24877606 http://dx.doi.org/10.1042/BSR20140021 |
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