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Polycystin 2 is increased in disease to protect against stress-induced cell death

Polycystin 2 (PC2 or TRPP1, formerly TRPP2) is a calcium-permeant Transient Receptor Potential (TRP) cation channel expressed primarily on the endoplasmic reticulum (ER) membrane and primary cilia of all cell and tissue types. Despite its ubiquitous expression throughout the body, studies of PC2 hav...

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Autores principales: Brill, Allison L., Fischer, Tom T., Walters, Jennifer M., Marlier, Arnaud, Sewanan, Lorenzo R., Wilson, Parker C., Johnson, Eric K., Moeckel, Gilbert, Cantley, Lloyd G., Campbell, Stuart G., Nerbonne, Jeanne M., Chung, Hee Jung, Robert, Marie E., Ehrlich, Barbara E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962458/
https://www.ncbi.nlm.nih.gov/pubmed/31941974
http://dx.doi.org/10.1038/s41598-019-57286-x
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author Brill, Allison L.
Fischer, Tom T.
Walters, Jennifer M.
Marlier, Arnaud
Sewanan, Lorenzo R.
Wilson, Parker C.
Johnson, Eric K.
Moeckel, Gilbert
Cantley, Lloyd G.
Campbell, Stuart G.
Nerbonne, Jeanne M.
Chung, Hee Jung
Robert, Marie E.
Ehrlich, Barbara E.
author_facet Brill, Allison L.
Fischer, Tom T.
Walters, Jennifer M.
Marlier, Arnaud
Sewanan, Lorenzo R.
Wilson, Parker C.
Johnson, Eric K.
Moeckel, Gilbert
Cantley, Lloyd G.
Campbell, Stuart G.
Nerbonne, Jeanne M.
Chung, Hee Jung
Robert, Marie E.
Ehrlich, Barbara E.
author_sort Brill, Allison L.
collection PubMed
description Polycystin 2 (PC2 or TRPP1, formerly TRPP2) is a calcium-permeant Transient Receptor Potential (TRP) cation channel expressed primarily on the endoplasmic reticulum (ER) membrane and primary cilia of all cell and tissue types. Despite its ubiquitous expression throughout the body, studies of PC2 have focused primarily on its role in the kidney, as mutations in PC2 lead to the development of autosomal dominant polycystic kidney disease (ADPKD), a debilitating condition for which there is no cure. However, the endogenous role that PC2 plays in the regulation of general cellular homeostasis remains unclear. In this study, we measure how PC2 expression changes in different pathological states, determine that its abundance is increased under conditions of cellular stress in multiple tissues including human disease, and conclude that PC2-deficient cells have increased susceptibility to cell death induced by stress. Our results offer new insight into the normal function of PC2 as a ubiquitous stress-sensitive protein whose expression is up-regulated in response to cell stress to protect against pathological cell death in multiple diseases.
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spelling pubmed-69624582020-01-23 Polycystin 2 is increased in disease to protect against stress-induced cell death Brill, Allison L. Fischer, Tom T. Walters, Jennifer M. Marlier, Arnaud Sewanan, Lorenzo R. Wilson, Parker C. Johnson, Eric K. Moeckel, Gilbert Cantley, Lloyd G. Campbell, Stuart G. Nerbonne, Jeanne M. Chung, Hee Jung Robert, Marie E. Ehrlich, Barbara E. Sci Rep Article Polycystin 2 (PC2 or TRPP1, formerly TRPP2) is a calcium-permeant Transient Receptor Potential (TRP) cation channel expressed primarily on the endoplasmic reticulum (ER) membrane and primary cilia of all cell and tissue types. Despite its ubiquitous expression throughout the body, studies of PC2 have focused primarily on its role in the kidney, as mutations in PC2 lead to the development of autosomal dominant polycystic kidney disease (ADPKD), a debilitating condition for which there is no cure. However, the endogenous role that PC2 plays in the regulation of general cellular homeostasis remains unclear. In this study, we measure how PC2 expression changes in different pathological states, determine that its abundance is increased under conditions of cellular stress in multiple tissues including human disease, and conclude that PC2-deficient cells have increased susceptibility to cell death induced by stress. Our results offer new insight into the normal function of PC2 as a ubiquitous stress-sensitive protein whose expression is up-regulated in response to cell stress to protect against pathological cell death in multiple diseases. Nature Publishing Group UK 2020-01-15 /pmc/articles/PMC6962458/ /pubmed/31941974 http://dx.doi.org/10.1038/s41598-019-57286-x Text en © The Author(s) 2020 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
Brill, Allison L.
Fischer, Tom T.
Walters, Jennifer M.
Marlier, Arnaud
Sewanan, Lorenzo R.
Wilson, Parker C.
Johnson, Eric K.
Moeckel, Gilbert
Cantley, Lloyd G.
Campbell, Stuart G.
Nerbonne, Jeanne M.
Chung, Hee Jung
Robert, Marie E.
Ehrlich, Barbara E.
Polycystin 2 is increased in disease to protect against stress-induced cell death
title Polycystin 2 is increased in disease to protect against stress-induced cell death
title_full Polycystin 2 is increased in disease to protect against stress-induced cell death
title_fullStr Polycystin 2 is increased in disease to protect against stress-induced cell death
title_full_unstemmed Polycystin 2 is increased in disease to protect against stress-induced cell death
title_short Polycystin 2 is increased in disease to protect against stress-induced cell death
title_sort polycystin 2 is increased in disease to protect against stress-induced cell death
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962458/
https://www.ncbi.nlm.nih.gov/pubmed/31941974
http://dx.doi.org/10.1038/s41598-019-57286-x
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