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Membrane capacitance recordings resolve dynamics and complexity of receptor-mediated endocytosis in Wnt signalling
Receptor-mediated endocytosis is an essential process in signalling pathways for activation of intracellular signalling cascades. One example is the Wnt signalling pathway that seems to depend on endocytosis of the ligand-receptor complex for initiation of Wnt signal transduction. To date, the roles...
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/PMC6736968/ https://www.ncbi.nlm.nih.gov/pubmed/31506500 http://dx.doi.org/10.1038/s41598-019-49082-4 |
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author | Bandmann, Vera Mirsanaye, Ann Schirin Schäfer, Johanna Thiel, Gerhard Holstein, Thomas Mikosch-Wersching, Melanie |
author_facet | Bandmann, Vera Mirsanaye, Ann Schirin Schäfer, Johanna Thiel, Gerhard Holstein, Thomas Mikosch-Wersching, Melanie |
author_sort | Bandmann, Vera |
collection | PubMed |
description | Receptor-mediated endocytosis is an essential process in signalling pathways for activation of intracellular signalling cascades. One example is the Wnt signalling pathway that seems to depend on endocytosis of the ligand-receptor complex for initiation of Wnt signal transduction. To date, the roles of different endocytic pathways in Wnt signalling, molecular players and the kinetics of the process remain unclear. Here, we monitored endocytosis in Wnt3a and Wnt5a-mediated signalling with membrane capacitance recordings of HEK293 cells. Our measurements revealed a swift and substantial increase in the number of endocytic vesicles. Extracellular Wnt ligands specifically triggered endocytotic activity, which started immediately upon ligand binding and ceased within a period of ten minutes. By using specific inhibitors, we were able to separate Wnt-induced endocytosis into two independent pathways. We demonstrate that canonical Wnt3a is taken up mainly by clathrin-independent endocytosis whereas noncanonical Wnt5a is exclusively regulated via clathrin-mediated endocytosis. Our findings show that membrane capacitance recordings allow the resolution of complex cellular processes in plasma membrane signalling pathways in great detail. |
format | Online Article Text |
id | pubmed-6736968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67369682019-09-20 Membrane capacitance recordings resolve dynamics and complexity of receptor-mediated endocytosis in Wnt signalling Bandmann, Vera Mirsanaye, Ann Schirin Schäfer, Johanna Thiel, Gerhard Holstein, Thomas Mikosch-Wersching, Melanie Sci Rep Article Receptor-mediated endocytosis is an essential process in signalling pathways for activation of intracellular signalling cascades. One example is the Wnt signalling pathway that seems to depend on endocytosis of the ligand-receptor complex for initiation of Wnt signal transduction. To date, the roles of different endocytic pathways in Wnt signalling, molecular players and the kinetics of the process remain unclear. Here, we monitored endocytosis in Wnt3a and Wnt5a-mediated signalling with membrane capacitance recordings of HEK293 cells. Our measurements revealed a swift and substantial increase in the number of endocytic vesicles. Extracellular Wnt ligands specifically triggered endocytotic activity, which started immediately upon ligand binding and ceased within a period of ten minutes. By using specific inhibitors, we were able to separate Wnt-induced endocytosis into two independent pathways. We demonstrate that canonical Wnt3a is taken up mainly by clathrin-independent endocytosis whereas noncanonical Wnt5a is exclusively regulated via clathrin-mediated endocytosis. Our findings show that membrane capacitance recordings allow the resolution of complex cellular processes in plasma membrane signalling pathways in great detail. Nature Publishing Group UK 2019-09-10 /pmc/articles/PMC6736968/ /pubmed/31506500 http://dx.doi.org/10.1038/s41598-019-49082-4 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 Bandmann, Vera Mirsanaye, Ann Schirin Schäfer, Johanna Thiel, Gerhard Holstein, Thomas Mikosch-Wersching, Melanie Membrane capacitance recordings resolve dynamics and complexity of receptor-mediated endocytosis in Wnt signalling |
title | Membrane capacitance recordings resolve dynamics and complexity of receptor-mediated endocytosis in Wnt signalling |
title_full | Membrane capacitance recordings resolve dynamics and complexity of receptor-mediated endocytosis in Wnt signalling |
title_fullStr | Membrane capacitance recordings resolve dynamics and complexity of receptor-mediated endocytosis in Wnt signalling |
title_full_unstemmed | Membrane capacitance recordings resolve dynamics and complexity of receptor-mediated endocytosis in Wnt signalling |
title_short | Membrane capacitance recordings resolve dynamics and complexity of receptor-mediated endocytosis in Wnt signalling |
title_sort | membrane capacitance recordings resolve dynamics and complexity of receptor-mediated endocytosis in wnt signalling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736968/ https://www.ncbi.nlm.nih.gov/pubmed/31506500 http://dx.doi.org/10.1038/s41598-019-49082-4 |
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