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Evidence for the mechanosensor function of filamin in tissue development

Cells integrate mechanical properties of their surroundings to form multicellular, three-dimensional tissues of appropriate size and spatial organisation. Actin cytoskeleton-linked proteins such as talin, vinculin and filamin function as mechanosensors in cells, but it has yet to be tested whether t...

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Autores principales: Huelsmann, Sven, Rintanen, Nina, Sethi, Ritika, Brown, Nicholas H., Ylänne, Jari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011733/
https://www.ncbi.nlm.nih.gov/pubmed/27597179
http://dx.doi.org/10.1038/srep32798
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author Huelsmann, Sven
Rintanen, Nina
Sethi, Ritika
Brown, Nicholas H.
Ylänne, Jari
author_facet Huelsmann, Sven
Rintanen, Nina
Sethi, Ritika
Brown, Nicholas H.
Ylänne, Jari
author_sort Huelsmann, Sven
collection PubMed
description Cells integrate mechanical properties of their surroundings to form multicellular, three-dimensional tissues of appropriate size and spatial organisation. Actin cytoskeleton-linked proteins such as talin, vinculin and filamin function as mechanosensors in cells, but it has yet to be tested whether the mechanosensitivity is important for their function in intact tissues. Here we tested, how filamin mechanosensing contributes to oogenesis in Drosophila. Mutations that require more or less force to open the mechanosensor region demonstrate that filamin mechanosensitivity is important for the maturation of actin-rich ring canals that are essential for Drosophila egg development. The open mutant was more tightly bound to the ring canal structure while the closed mutant dissociated more frequently. Thus, our results show that an appropriate level of mechanical sensitivity is required for filamins’ function and dynamics during Drosophila egg growth and support the structure-based model in which the opening and closing of the mechanosensor region regulates filamin binding to cellular components.
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spelling pubmed-50117332016-09-12 Evidence for the mechanosensor function of filamin in tissue development Huelsmann, Sven Rintanen, Nina Sethi, Ritika Brown, Nicholas H. Ylänne, Jari Sci Rep Article Cells integrate mechanical properties of their surroundings to form multicellular, three-dimensional tissues of appropriate size and spatial organisation. Actin cytoskeleton-linked proteins such as talin, vinculin and filamin function as mechanosensors in cells, but it has yet to be tested whether the mechanosensitivity is important for their function in intact tissues. Here we tested, how filamin mechanosensing contributes to oogenesis in Drosophila. Mutations that require more or less force to open the mechanosensor region demonstrate that filamin mechanosensitivity is important for the maturation of actin-rich ring canals that are essential for Drosophila egg development. The open mutant was more tightly bound to the ring canal structure while the closed mutant dissociated more frequently. Thus, our results show that an appropriate level of mechanical sensitivity is required for filamins’ function and dynamics during Drosophila egg growth and support the structure-based model in which the opening and closing of the mechanosensor region regulates filamin binding to cellular components. Nature Publishing Group 2016-09-06 /pmc/articles/PMC5011733/ /pubmed/27597179 http://dx.doi.org/10.1038/srep32798 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Huelsmann, Sven
Rintanen, Nina
Sethi, Ritika
Brown, Nicholas H.
Ylänne, Jari
Evidence for the mechanosensor function of filamin in tissue development
title Evidence for the mechanosensor function of filamin in tissue development
title_full Evidence for the mechanosensor function of filamin in tissue development
title_fullStr Evidence for the mechanosensor function of filamin in tissue development
title_full_unstemmed Evidence for the mechanosensor function of filamin in tissue development
title_short Evidence for the mechanosensor function of filamin in tissue development
title_sort evidence for the mechanosensor function of filamin in tissue development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011733/
https://www.ncbi.nlm.nih.gov/pubmed/27597179
http://dx.doi.org/10.1038/srep32798
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