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Regulation of inflammatory responses by dynamic subcellular localization of RNA-binding protein Arid5a
Adenine-thymine (AT)-rich interactive domain 5a (Arid5a) is an RNA-binding protein found in the cytoplasm and nucleus of normally growing cells. Although Arid5a is known to play an important role in immune regulation, whether and how Arid5a subcellular localization impacts immune regulation has rema...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819453/ https://www.ncbi.nlm.nih.gov/pubmed/29358370 http://dx.doi.org/10.1073/pnas.1719921115 |
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author | Higa, Mitsuru Oka, Masahiro Fujihara, Yoshitaka Masuda, Kazuya Yoneda, Yoshihiro Kishimoto, Tadamitsu |
author_facet | Higa, Mitsuru Oka, Masahiro Fujihara, Yoshitaka Masuda, Kazuya Yoneda, Yoshihiro Kishimoto, Tadamitsu |
author_sort | Higa, Mitsuru |
collection | PubMed |
description | Adenine-thymine (AT)-rich interactive domain 5a (Arid5a) is an RNA-binding protein found in the cytoplasm and nucleus of normally growing cells. Although Arid5a is known to play an important role in immune regulation, whether and how Arid5a subcellular localization impacts immune regulation has remained unclear. In this study, we generated Arid5a transgenic (TG) mice to address this question. While ectopic Arid5a overexpression did not affect expression of inflammatory cytokines under unstimulated conditions, significantly higher levels of inflammatory cytokines, such as IL-6, were produced in response to lipopolysaccharide (LPS) stimulation. Consistent with this, TG mice were more sensitive to LPS treatment than wild-type mice. We also found that Arid5a is imported into the nucleus via a classical importin-α/β1–mediated pathway. On stimulation, nuclear Arid5a levels were decreased, while there was a concomitant increase in cytoplasmic Arid5a. Arid5a is associated with up-frameshift protein 1, and its nuclear export is regulated by a nuclear export receptor, chromosomal region maintenance 1. Taken together, these data indicate that Arid5a is a dynamic protein that translocates to the cytoplasm from the nucleus so as to properly exert its dual function in mRNA stabilization and transcriptional regulation during inflammatory conditions. |
format | Online Article Text |
id | pubmed-5819453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-58194532018-02-21 Regulation of inflammatory responses by dynamic subcellular localization of RNA-binding protein Arid5a Higa, Mitsuru Oka, Masahiro Fujihara, Yoshitaka Masuda, Kazuya Yoneda, Yoshihiro Kishimoto, Tadamitsu Proc Natl Acad Sci U S A PNAS Plus Adenine-thymine (AT)-rich interactive domain 5a (Arid5a) is an RNA-binding protein found in the cytoplasm and nucleus of normally growing cells. Although Arid5a is known to play an important role in immune regulation, whether and how Arid5a subcellular localization impacts immune regulation has remained unclear. In this study, we generated Arid5a transgenic (TG) mice to address this question. While ectopic Arid5a overexpression did not affect expression of inflammatory cytokines under unstimulated conditions, significantly higher levels of inflammatory cytokines, such as IL-6, were produced in response to lipopolysaccharide (LPS) stimulation. Consistent with this, TG mice were more sensitive to LPS treatment than wild-type mice. We also found that Arid5a is imported into the nucleus via a classical importin-α/β1–mediated pathway. On stimulation, nuclear Arid5a levels were decreased, while there was a concomitant increase in cytoplasmic Arid5a. Arid5a is associated with up-frameshift protein 1, and its nuclear export is regulated by a nuclear export receptor, chromosomal region maintenance 1. Taken together, these data indicate that Arid5a is a dynamic protein that translocates to the cytoplasm from the nucleus so as to properly exert its dual function in mRNA stabilization and transcriptional regulation during inflammatory conditions. National Academy of Sciences 2018-02-06 2018-01-22 /pmc/articles/PMC5819453/ /pubmed/29358370 http://dx.doi.org/10.1073/pnas.1719921115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | PNAS Plus Higa, Mitsuru Oka, Masahiro Fujihara, Yoshitaka Masuda, Kazuya Yoneda, Yoshihiro Kishimoto, Tadamitsu Regulation of inflammatory responses by dynamic subcellular localization of RNA-binding protein Arid5a |
title | Regulation of inflammatory responses by dynamic subcellular localization of RNA-binding protein Arid5a |
title_full | Regulation of inflammatory responses by dynamic subcellular localization of RNA-binding protein Arid5a |
title_fullStr | Regulation of inflammatory responses by dynamic subcellular localization of RNA-binding protein Arid5a |
title_full_unstemmed | Regulation of inflammatory responses by dynamic subcellular localization of RNA-binding protein Arid5a |
title_short | Regulation of inflammatory responses by dynamic subcellular localization of RNA-binding protein Arid5a |
title_sort | regulation of inflammatory responses by dynamic subcellular localization of rna-binding protein arid5a |
topic | PNAS Plus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819453/ https://www.ncbi.nlm.nih.gov/pubmed/29358370 http://dx.doi.org/10.1073/pnas.1719921115 |
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