Florian Geisler
The intestinal intermediate filament network responds to and protects against microbial insults and toxins
Geisler, Florian; Coch, Richard A.; Richardson, Christine; Goldberg, Martin; Denecke, Bernd; Bossinger, Olaf; Leube, Rudolf E.
Authors
Richard A. Coch
Christine Richardson
Professor Martin Goldberg m.w.goldberg@durham.ac.uk
Professor
Bernd Denecke
Olaf Bossinger
Rudolf E. Leube
Abstract
The enrichment of intermediate filaments in the apical cytoplasm of intestinal cells is evolutionary conserved forming a sheath that is anchored to apical junctions and positioned below the microvillar brush border suggestive of a protective intracellular barrier function. To test this, we used C. elegans, whose intestinal cells are endowed with a particularly dense intermediate filament-rich layer that is referred to as the endotube. We find alterations in endotube structure and intermediate filament expression upon infection with nematicidal Bacillus thuringiensis or treatment with its major pore-forming toxin crystal protein Cry5B. Endotube impairment due to defined genetic mutations of intermediate filaments and their regulators results in increased Cry5B sensitivity as evidenced by elevated larval arrest, prolonged time of larval development and reduced survival. Phenotype severity reflects the severity of endotube alterations and correlates with reduced rescue upon toxin removal. The results provide in vivo evidence for a major protective role of a properly configured intermediate filament network as an intracellular barrier in intestinal cells. This notion is further supported by increased sensitivity of endotube mutants to oxidative and osmotic stress.
Citation
Geisler, F., Coch, R. A., Richardson, C., Goldberg, M., Denecke, B., Bossinger, O., & Leube, R. E. (2019). The intestinal intermediate filament network responds to and protects against microbial insults and toxins. Development, 146(2), Article dev.169482. https://doi.org/10.1242/dev.169482
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 19, 2018 |
Online Publication Date | Jan 23, 2019 |
Publication Date | Jan 15, 2019 |
Deposit Date | Jan 14, 2019 |
Publicly Available Date | Jan 23, 2020 |
Journal | Development. |
Print ISSN | 0950-1991 |
Electronic ISSN | 1477-9129 |
Publisher | The Company of Biologists |
Peer Reviewed | Peer Reviewed |
Volume | 146 |
Issue | 2 |
Article Number | dev.169482 |
DOI | https://doi.org/10.1242/dev.169482 |
Public URL | https://durham-repository.worktribe.com/output/1305408 |
Files
Published Journal Article
(3.8 Mb)
PDF
You might also like
STING nuclear partners contribute to innate immune signaling responses
(2021)
Journal Article
BBLN-1 is essential for intermediate filament organization and apical membrane morphology
(2021)
Journal Article
Agitation Modules: Flexible Means to Accelerate Automated Freeze Substitution
(2018)
Journal Article
Downloadable Citations
About Durham Research Online (DRO)
Administrator e-mail: dro.admin@durham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search