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Transcription factor EB regulates phosphatidylinositol-3-phosphate levels that control lysosome positioning in the bladder cancer model

Lysosomes orchestrate degradation and recycling of exogenous and endogenous material thus controlling cellular homeostasis. Little is known how this organelle changes during cancer. Here we investigate the intracellular landscape of lysosomes in a cellular model of bladder cancer. Employing standard...

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Autores principales: Mathur, Pallavi, De Barros Santos, Camilla, Lachuer, Hugo, Patat, Julie, Latgé, Bruno, Radvanyi, François, Goud, Bruno, Schauer, Kristine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884284/
https://www.ncbi.nlm.nih.gov/pubmed/36709383
http://dx.doi.org/10.1038/s42003-023-04501-1
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author Mathur, Pallavi
De Barros Santos, Camilla
Lachuer, Hugo
Patat, Julie
Latgé, Bruno
Radvanyi, François
Goud, Bruno
Schauer, Kristine
author_facet Mathur, Pallavi
De Barros Santos, Camilla
Lachuer, Hugo
Patat, Julie
Latgé, Bruno
Radvanyi, François
Goud, Bruno
Schauer, Kristine
author_sort Mathur, Pallavi
collection PubMed
description Lysosomes orchestrate degradation and recycling of exogenous and endogenous material thus controlling cellular homeostasis. Little is known how this organelle changes during cancer. Here we investigate the intracellular landscape of lysosomes in a cellular model of bladder cancer. Employing standardized cell culture on micropatterns we identify a phenotype of peripheral lysosome positioning prevailing in bladder cancer cell lines but not normal urothelium. We show that lysosome positioning is controlled by phosphatidylinositol-3-phosphate (PtdIns3P) levels on endomembranes which recruit FYVE-domain containing proteins for lysosomal dispersion. We identify transcription factor EB (TFEB) as an upstream regulator of PtdIns3P production by VPS34 that is activated in aggressive bladder cancer cells with peripheral lysosomes. This conceptually clarifies the dual role of TFEB as regulator of endosomal maturation and autophagy, two distinct processes controlled by PtdIns3P. Altogether, our findings uncover peripheral lysosome positioning, resulting from PtdIns3P production downstream of TFEB activation, as a potential biomarker for bladder cancer.
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spelling pubmed-98842842023-01-30 Transcription factor EB regulates phosphatidylinositol-3-phosphate levels that control lysosome positioning in the bladder cancer model Mathur, Pallavi De Barros Santos, Camilla Lachuer, Hugo Patat, Julie Latgé, Bruno Radvanyi, François Goud, Bruno Schauer, Kristine Commun Biol Article Lysosomes orchestrate degradation and recycling of exogenous and endogenous material thus controlling cellular homeostasis. Little is known how this organelle changes during cancer. Here we investigate the intracellular landscape of lysosomes in a cellular model of bladder cancer. Employing standardized cell culture on micropatterns we identify a phenotype of peripheral lysosome positioning prevailing in bladder cancer cell lines but not normal urothelium. We show that lysosome positioning is controlled by phosphatidylinositol-3-phosphate (PtdIns3P) levels on endomembranes which recruit FYVE-domain containing proteins for lysosomal dispersion. We identify transcription factor EB (TFEB) as an upstream regulator of PtdIns3P production by VPS34 that is activated in aggressive bladder cancer cells with peripheral lysosomes. This conceptually clarifies the dual role of TFEB as regulator of endosomal maturation and autophagy, two distinct processes controlled by PtdIns3P. Altogether, our findings uncover peripheral lysosome positioning, resulting from PtdIns3P production downstream of TFEB activation, as a potential biomarker for bladder cancer. Nature Publishing Group UK 2023-01-28 /pmc/articles/PMC9884284/ /pubmed/36709383 http://dx.doi.org/10.1038/s42003-023-04501-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mathur, Pallavi
De Barros Santos, Camilla
Lachuer, Hugo
Patat, Julie
Latgé, Bruno
Radvanyi, François
Goud, Bruno
Schauer, Kristine
Transcription factor EB regulates phosphatidylinositol-3-phosphate levels that control lysosome positioning in the bladder cancer model
title Transcription factor EB regulates phosphatidylinositol-3-phosphate levels that control lysosome positioning in the bladder cancer model
title_full Transcription factor EB regulates phosphatidylinositol-3-phosphate levels that control lysosome positioning in the bladder cancer model
title_fullStr Transcription factor EB regulates phosphatidylinositol-3-phosphate levels that control lysosome positioning in the bladder cancer model
title_full_unstemmed Transcription factor EB regulates phosphatidylinositol-3-phosphate levels that control lysosome positioning in the bladder cancer model
title_short Transcription factor EB regulates phosphatidylinositol-3-phosphate levels that control lysosome positioning in the bladder cancer model
title_sort transcription factor eb regulates phosphatidylinositol-3-phosphate levels that control lysosome positioning in the bladder cancer model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884284/
https://www.ncbi.nlm.nih.gov/pubmed/36709383
http://dx.doi.org/10.1038/s42003-023-04501-1
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