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Sensory primary cilium is a responsive cAMP microdomain in renal epithelia
Primary cilia are hair-like cellular extensions that sense microenvironmental signals surrounding cells. The role of adenylyl cyclases in ciliary function has been of interest because the product of adenylyl cyclase activity, cAMP, is relevant to cilia-related diseases. In the present study, we show...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484033/ https://www.ncbi.nlm.nih.gov/pubmed/31024067 http://dx.doi.org/10.1038/s41598-019-43002-2 |
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author | Sherpa, Rinzhin T. Mohieldin, Ashraf M. Pala, Rajasekharreddy Wachten, Dagmar Ostrom, Rennolds S. Nauli, Surya M. |
author_facet | Sherpa, Rinzhin T. Mohieldin, Ashraf M. Pala, Rajasekharreddy Wachten, Dagmar Ostrom, Rennolds S. Nauli, Surya M. |
author_sort | Sherpa, Rinzhin T. |
collection | PubMed |
description | Primary cilia are hair-like cellular extensions that sense microenvironmental signals surrounding cells. The role of adenylyl cyclases in ciliary function has been of interest because the product of adenylyl cyclase activity, cAMP, is relevant to cilia-related diseases. In the present study, we show that vasopressin receptor type-2 (V2R) is localized to cilia in kidney epithelial cells. Pharmacologic inhibition of V2R with tolvaptan increases ciliary length and mechanosensory function. Genetic knockdown of V2R, however, does not have any effect on ciliary length, although the effect of tolvaptan on ciliary length is dampened. Our study reveals that tolvaptan may have a cilia-specific effect independent of V2R or verapamil-sensitive calcium channels. Live-imaging of single cilia shows that V2R activation increases cilioplasmic and cytoplasmic cAMP levels, whereas tolvaptan mediates cAMP changes only in a cilia-specific manner. Furthermore, fluid-shear stress decreases cilioplasmic, but not cytoplasmic cAMP levels. Our data indicate that cilioplasmic and cytoplasmic cAMP levels are differentially modulated. We propose that the cilium is a critical sensor acting as a responsive cAMP microcompartment during physiologically relevant stimuli. |
format | Online Article Text |
id | pubmed-6484033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64840332019-05-13 Sensory primary cilium is a responsive cAMP microdomain in renal epithelia Sherpa, Rinzhin T. Mohieldin, Ashraf M. Pala, Rajasekharreddy Wachten, Dagmar Ostrom, Rennolds S. Nauli, Surya M. Sci Rep Article Primary cilia are hair-like cellular extensions that sense microenvironmental signals surrounding cells. The role of adenylyl cyclases in ciliary function has been of interest because the product of adenylyl cyclase activity, cAMP, is relevant to cilia-related diseases. In the present study, we show that vasopressin receptor type-2 (V2R) is localized to cilia in kidney epithelial cells. Pharmacologic inhibition of V2R with tolvaptan increases ciliary length and mechanosensory function. Genetic knockdown of V2R, however, does not have any effect on ciliary length, although the effect of tolvaptan on ciliary length is dampened. Our study reveals that tolvaptan may have a cilia-specific effect independent of V2R or verapamil-sensitive calcium channels. Live-imaging of single cilia shows that V2R activation increases cilioplasmic and cytoplasmic cAMP levels, whereas tolvaptan mediates cAMP changes only in a cilia-specific manner. Furthermore, fluid-shear stress decreases cilioplasmic, but not cytoplasmic cAMP levels. Our data indicate that cilioplasmic and cytoplasmic cAMP levels are differentially modulated. We propose that the cilium is a critical sensor acting as a responsive cAMP microcompartment during physiologically relevant stimuli. Nature Publishing Group UK 2019-04-25 /pmc/articles/PMC6484033/ /pubmed/31024067 http://dx.doi.org/10.1038/s41598-019-43002-2 Text en © The Author(s) 2019 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 Sherpa, Rinzhin T. Mohieldin, Ashraf M. Pala, Rajasekharreddy Wachten, Dagmar Ostrom, Rennolds S. Nauli, Surya M. Sensory primary cilium is a responsive cAMP microdomain in renal epithelia |
title | Sensory primary cilium is a responsive cAMP microdomain in renal epithelia |
title_full | Sensory primary cilium is a responsive cAMP microdomain in renal epithelia |
title_fullStr | Sensory primary cilium is a responsive cAMP microdomain in renal epithelia |
title_full_unstemmed | Sensory primary cilium is a responsive cAMP microdomain in renal epithelia |
title_short | Sensory primary cilium is a responsive cAMP microdomain in renal epithelia |
title_sort | sensory primary cilium is a responsive camp microdomain in renal epithelia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484033/ https://www.ncbi.nlm.nih.gov/pubmed/31024067 http://dx.doi.org/10.1038/s41598-019-43002-2 |
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