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Cyclosporine A binding to COX-2 reveals a novel signaling pathway that activates the IRE1α unfolded protein response sensor
Cyclosporine, a widely used immunosuppressant in organ transplantation and in treatment of various autoimmune diseases, activates the unfolded protein response (UPR), an ER stress coping response. In this study we discovered a new and unanticipated cyclosporine-dependent signaling pathway, with cycl...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232179/ https://www.ncbi.nlm.nih.gov/pubmed/30420769 http://dx.doi.org/10.1038/s41598-018-34891-w |
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author | Groenendyk, Jody Paskevicius, Tautvydas Urra, Hery Viricel, Clement Wang, Kui Barakat, Khaled Hetz, Claudio Kurgan, Lukasz Agellon, Luis B. Michalak, Marek |
author_facet | Groenendyk, Jody Paskevicius, Tautvydas Urra, Hery Viricel, Clement Wang, Kui Barakat, Khaled Hetz, Claudio Kurgan, Lukasz Agellon, Luis B. Michalak, Marek |
author_sort | Groenendyk, Jody |
collection | PubMed |
description | Cyclosporine, a widely used immunosuppressant in organ transplantation and in treatment of various autoimmune diseases, activates the unfolded protein response (UPR), an ER stress coping response. In this study we discovered a new and unanticipated cyclosporine-dependent signaling pathway, with cyclosporine triggering direct activation of the UPR. COX-2 binds to and activates IRE1α, leading to IRE1α splicing of XBP1 mRNA. Molecular interaction and modeling analyses identified a novel interaction site for cyclosporine with COX-2 which caused enhancement of COX-2 enzymatic activity required for activation of the IRE1α branch of the UPR. Cyclosporine-dependent activation of COX-2 and IRE1α in mice indicated that cyclosporine-COX-2-IRE1α signaling pathway was functional in vivo. These findings identify COX-2 as a new IRE1α binding partner and regulator of the IRE1α branch of the UPR pathway, and establishes the mechanism underlying cytotoxicity associated with chronic cyclosporine exposure. |
format | Online Article Text |
id | pubmed-6232179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62321792018-11-28 Cyclosporine A binding to COX-2 reveals a novel signaling pathway that activates the IRE1α unfolded protein response sensor Groenendyk, Jody Paskevicius, Tautvydas Urra, Hery Viricel, Clement Wang, Kui Barakat, Khaled Hetz, Claudio Kurgan, Lukasz Agellon, Luis B. Michalak, Marek Sci Rep Article Cyclosporine, a widely used immunosuppressant in organ transplantation and in treatment of various autoimmune diseases, activates the unfolded protein response (UPR), an ER stress coping response. In this study we discovered a new and unanticipated cyclosporine-dependent signaling pathway, with cyclosporine triggering direct activation of the UPR. COX-2 binds to and activates IRE1α, leading to IRE1α splicing of XBP1 mRNA. Molecular interaction and modeling analyses identified a novel interaction site for cyclosporine with COX-2 which caused enhancement of COX-2 enzymatic activity required for activation of the IRE1α branch of the UPR. Cyclosporine-dependent activation of COX-2 and IRE1α in mice indicated that cyclosporine-COX-2-IRE1α signaling pathway was functional in vivo. These findings identify COX-2 as a new IRE1α binding partner and regulator of the IRE1α branch of the UPR pathway, and establishes the mechanism underlying cytotoxicity associated with chronic cyclosporine exposure. Nature Publishing Group UK 2018-11-12 /pmc/articles/PMC6232179/ /pubmed/30420769 http://dx.doi.org/10.1038/s41598-018-34891-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Groenendyk, Jody Paskevicius, Tautvydas Urra, Hery Viricel, Clement Wang, Kui Barakat, Khaled Hetz, Claudio Kurgan, Lukasz Agellon, Luis B. Michalak, Marek Cyclosporine A binding to COX-2 reveals a novel signaling pathway that activates the IRE1α unfolded protein response sensor |
title | Cyclosporine A binding to COX-2 reveals a novel signaling pathway that activates the IRE1α unfolded protein response sensor |
title_full | Cyclosporine A binding to COX-2 reveals a novel signaling pathway that activates the IRE1α unfolded protein response sensor |
title_fullStr | Cyclosporine A binding to COX-2 reveals a novel signaling pathway that activates the IRE1α unfolded protein response sensor |
title_full_unstemmed | Cyclosporine A binding to COX-2 reveals a novel signaling pathway that activates the IRE1α unfolded protein response sensor |
title_short | Cyclosporine A binding to COX-2 reveals a novel signaling pathway that activates the IRE1α unfolded protein response sensor |
title_sort | cyclosporine a binding to cox-2 reveals a novel signaling pathway that activates the ire1α unfolded protein response sensor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232179/ https://www.ncbi.nlm.nih.gov/pubmed/30420769 http://dx.doi.org/10.1038/s41598-018-34891-w |
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