Evidence for the mechanosensor function of filamin in tissue development
Abstract
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.
Main Authors
Format
Articles
Research article
Published
2016
Series
Subjects
Publication in research information system
Publisher
Nature Publishing Group
The permanent address of the publication
https://urn.fi/URN:NBN:fi:jyu-201609084044Use this for linking
Review status
Peer reviewed
ISSN
2045-2322
DOI
https://doi.org/10.1038/srep32798
Language
English
Published in
Scientific Reports
Citation
- Huelsmann, S., Rintanen, N., Sethi, R., Brown, N. H., & Ylänne, J. (2016). Evidence for the mechanosensor function of filamin in tissue development. Scientific Reports, 6, Article 32798. https://doi.org/10.1038/srep32798
Funder(s)
Research Council of Finland
Funding program(s)
Akatemiahanke, SA
Academy Project, AoF

Additional information about funding
This work was funded by Academy of Finland grants 135473, 138327 and 278668 to J.Y., Wellcome Trust grant 086451 to N.H.B., and Gurdon Institute core funding from the Wellcome Trust (092096) and Cancer Research UK (C6946/A14492).
Copyright© the Authors, 2016. This is an open access article distributed under the terms of a Creative Commons License.