Evidence map›Paper›PMID 32081918›Full record

ArticleScientific reports2020

Intestinal intermediate filament polypeptides in C. elegans: Common and isotype-specific contributions to intestinal ultrastructure and function.

Florian Geisler, Richard A Coch, Christine Richardson, Martin Goldberg, Carlo Bevilacqua, Robert Prevedel, Rudolf E Leube

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  10. Epithelial morphogenesis, tubulogenesis and forces in organogenesis.Current topics in developmental biology · 2021
    Review
  11. Article
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  13. Journal of developmental biology · 2020
    Review
  14. A Series of Tubes: TheJournal of developmental biology · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Florian GeislerInstitute of Molecular and Cellular Anatomy, RWTH Aachen University, Aachen, Germany.
Richard A CochInstitute of Molecular and Cellular Anatomy, RWTH Aachen University, Aachen, Germany.
Christine RichardsonSchool of Biological and Biomedical Sciences, Durham University, Durham, United Kingdom.ORCID http://orcid.org/0000-0003-2622-2261
Martin GoldbergSchool of Biological and Biomedical Sciences, Durham University, Durham, United Kingdom.
Carlo BevilacquaCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Collaboration for joint PhD degree between EMBL and Heidelberg University, Faculty of Biosciences, Heidelberg, Germany.ORCID http://orcid.org/0000-0001-9084-0641
Robert PrevedelCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, Germany.ORCID http://orcid.org/0000-0003-3366-4703
Rudolf E LeubeInstitute of Molecular and Cellular Anatomy, RWTH Aachen University, Aachen, Germany. rleube@ukaachen.de.ORCID http://orcid.org/0000-0002-5519-7379
RWTH Aachen University · DEDurham University · GBEuropean Molecular Biology Laboratory · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The abundance and diversity of intermediate filaments (IFs) in the C. elegans intestine indicate important contributions to intestinal function and organismal wellbeing. Fluorescent IF reporters localize below the actin-rich brush border and are highly enriched in the lumen-enveloping endotube, which is attached to the C. elegans apical junction. Mapping intestinal viscoelasticity by contact-free Brillouin microscopy reveals that the IF-rich endotube is positioned at the interface between the stiff brush border and soft cytoplasm suggesting a mechanical buffering function to deal with the frequent luminal distortions occurring during food intake and movement. In accordance, depletion of IFB-2, IFC-2 and IFD-2 leads to intestinal lumen dilation although depletion of IFC-1, IFD-1 and IFP-1 do not. Ultrastructural analyses of loss of function mutants further show that IFC-2 mutants have a rarefied endotube and IFB-2 mutants lack an endotube altogether. Remarkably, almost all IFB-2- and IFC-2-deficient animals develop to fertile adults. But developmental retardation, reduced brood size, altered survival and increased sensitivity to microbial toxin, osmotic and oxidative stress are seen in both mutants albeit to different degrees. Taken together, we propose that individual intestinal IF polypeptides contribute in different ways to endotube morphogenesis and cooperate to cope with changing environments.

Indexed as

Actin CytoskeletonActinsAnimalsBacterial ProteinsCaenorhabditis elegansCaenorhabditis elegans ProteinsCytoskeletonElasticityGreen Fluorescent ProteinsIntermediate Filament ProteinsIntermediate FilamentsIntestinal MucosaIntestinesLuminescent ProteinsMicrovilliMutationActinsBacterial ProteinsCaenorhabditis elegans ProteinsCyan Fluorescent ProteinGreen Fluorescent ProteinsIntermediate Filament ProteinsLuminescent Proteinsyellow fluorescent protein, Bacteria

Identifiers

PMID32081918
PMCPMC7035338
OpenAlexW3006709644

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.