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The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes
Two-pore channels (TPCs) are localized in endo-lysosomal compartments and assumed to play an important role for vesicular fusion and endosomal trafficking. Recently, it has been shown that both TPC1 and 2 were required for host cell entry and pathogenicity of Ebola viruses. Here, we investigate the...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577145/ https://www.ncbi.nlm.nih.gov/pubmed/28855648 http://dx.doi.org/10.1038/s41598-017-10607-4 |
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author | Castonguay, Jan Orth, Joachim H. C. Müller, Thomas Sleman, Faten Grimm, Christian Wahl-Schott, Christian Biel, Martin Mallmann, Robert Theodor Bildl, Wolfgang Schulte, Uwe Klugbauer, Norbert |
author_facet | Castonguay, Jan Orth, Joachim H. C. Müller, Thomas Sleman, Faten Grimm, Christian Wahl-Schott, Christian Biel, Martin Mallmann, Robert Theodor Bildl, Wolfgang Schulte, Uwe Klugbauer, Norbert |
author_sort | Castonguay, Jan |
collection | PubMed |
description | Two-pore channels (TPCs) are localized in endo-lysosomal compartments and assumed to play an important role for vesicular fusion and endosomal trafficking. Recently, it has been shown that both TPC1 and 2 were required for host cell entry and pathogenicity of Ebola viruses. Here, we investigate the cellular function of TPC1 using protein toxins as model substrates for distinct endosomal processing routes. Toxin uptake and activation through early endosomes but not processing through other compartments were reduced in TPC1 knockout cells. Detailed co-localization studies with subcellular markers confirmed predominant localization of TPC1 to early and recycling endosomes. Proteomic analysis of native TPC1 channels finally identified direct interaction with a distinct set of syntaxins involved in fusion of intracellular vesicles. Together, our results demonstrate a general role of TPC1 for uptake and processing of proteins in early and recycling endosomes, likely by providing high local Ca(2+) concentrations required for SNARE-mediated vesicle fusion. |
format | Online Article Text |
id | pubmed-5577145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55771452017-09-01 The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes Castonguay, Jan Orth, Joachim H. C. Müller, Thomas Sleman, Faten Grimm, Christian Wahl-Schott, Christian Biel, Martin Mallmann, Robert Theodor Bildl, Wolfgang Schulte, Uwe Klugbauer, Norbert Sci Rep Article Two-pore channels (TPCs) are localized in endo-lysosomal compartments and assumed to play an important role for vesicular fusion and endosomal trafficking. Recently, it has been shown that both TPC1 and 2 were required for host cell entry and pathogenicity of Ebola viruses. Here, we investigate the cellular function of TPC1 using protein toxins as model substrates for distinct endosomal processing routes. Toxin uptake and activation through early endosomes but not processing through other compartments were reduced in TPC1 knockout cells. Detailed co-localization studies with subcellular markers confirmed predominant localization of TPC1 to early and recycling endosomes. Proteomic analysis of native TPC1 channels finally identified direct interaction with a distinct set of syntaxins involved in fusion of intracellular vesicles. Together, our results demonstrate a general role of TPC1 for uptake and processing of proteins in early and recycling endosomes, likely by providing high local Ca(2+) concentrations required for SNARE-mediated vesicle fusion. Nature Publishing Group UK 2017-08-30 /pmc/articles/PMC5577145/ /pubmed/28855648 http://dx.doi.org/10.1038/s41598-017-10607-4 Text en © The Author(s) 2017 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 Castonguay, Jan Orth, Joachim H. C. Müller, Thomas Sleman, Faten Grimm, Christian Wahl-Schott, Christian Biel, Martin Mallmann, Robert Theodor Bildl, Wolfgang Schulte, Uwe Klugbauer, Norbert The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes |
title | The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes |
title_full | The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes |
title_fullStr | The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes |
title_full_unstemmed | The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes |
title_short | The two-pore channel TPC1 is required for efficient protein processing through early and recycling endosomes |
title_sort | two-pore channel tpc1 is required for efficient protein processing through early and recycling endosomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577145/ https://www.ncbi.nlm.nih.gov/pubmed/28855648 http://dx.doi.org/10.1038/s41598-017-10607-4 |
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