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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...

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Autores principales: Groenendyk, Jody, Paskevicius, Tautvydas, Urra, Hery, Viricel, Clement, Wang, Kui, Barakat, Khaled, Hetz, Claudio, Kurgan, Lukasz, Agellon, Luis B., Michalak, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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