Evidence map›Paper›PMID 21421847›Full record

ArticleJournal of lipid research2011

Fluorescence-based fixative and vital staining of lipid droplets in Caenorhabditis elegans reveal fat stores using microscopy and flow cytometry approaches.

Maja Klapper, Madeleine Ehmke, Daniela Palgunow, Mike Böhme, Christian Matthäus, Gero Bergner, Benjamin Dietzek, Jürgen Popp, Frank Döring

Abstract read
In one paragraph

Article in Journal of lipid research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
–field-weighted citation impact
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

50 citing papers in PubMed.

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  7. Application ofInternational journal of molecular sciences · 2023
    Review
  8. Identifying lipid particle sub-types in liveFrontiers in chemistry · 2023
    Article
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  20. Methylmercury Induces Metabolic Alterations in Caenorhabditis elegans: Role for C/EBP Transcription Factor.Toxicological sciences : an official journal of the Society of Toxicology · 2020
    Article
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

9 authors.

Maja KlapperInstitute of Human Nutrition and Food Science, Research Group Molecular Prevention, University of Kiel, Kiel, Germany.
Madeleine EhmkeInstitute of Human Nutrition and Food Science, Research Group Molecular Prevention, University of Kiel, Kiel, Germany.
Daniela PalgunowInstitute of Human Nutrition and Food Science, Research Group Molecular Prevention, University of Kiel, Kiel, Germany.
Mike BöhmeInstitute of Human Nutrition and Food Science, Research Group Molecular Prevention, University of Kiel, Kiel, Germany.
Christian MatthäusInstitute of Photonic Technology, Jena, Germany.
Gero BergnerInstitute of Photonic Technology, Jena, Germany.
Benjamin DietzekInstitute of Photonic Technology, Jena, Germany.
Jürgen PoppInstitute of Photonic Technology, Jena, Germany.
Frank DöringInstitute of Human Nutrition and Food Science, Research Group Molecular Prevention, University of Kiel, Kiel, Germany. Electronic address: fdoering@molprev.uni-kiel.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The proportions of body fat and fat-free mass are determining factors of adiposity-associated diseases. Work in Caenorhabditis elegans has revealed evolutionarily conserved pathways of fat metabolism. Nevertheless, analysis of body composition and fat distribution in the nematodes has only been partially unraveled because of methodological difficulties. We characterized metabolic C. elegans mutants by using novel and feasible BODIPY 493/503-based fat staining and flow cytometry approaches. Fixative as well as vital BODIPY staining procedures visualize major fat stores, preserve native lipid droplet morphology, and allow quantification of fat content per body volume of individual worms. Colocalization studies using coherent anti-Stokes Raman scattering microscopy, Raman microspectroscopy, and imaging of lysosome-related organelles as well as biochemical measurement confirm our approaches. We found that the fat-to-volume ratio of dietary restriction, TGF-β, and germline mutants are specific for each strain. In contrast, the proportion of fat-free mass is constant between the mutants, although their volumes differ by a factor of 3. Our approaches enable sensitive, accurate, and high-throughput assessment of adiposity in large C. elegans populations at a single-worm level.

Indexed as

AdiposityHigh-Throughput Screening AssaysAdipose TissueAnimalsAzo CompoundsBoron CompoundsCaenorhabditis elegansDisease Models, AnimalFixativesFlow CytometryFluorescenceGerm-Line MutationLipid MetabolismMicroscopyObesitySpecies Specificity4,4-difluoro-4-bora-3a,4a-diaza-s-indaceneAzo CompoundsBoron CompoundsFixativesoil red OTransforming Growth Factor beta

Identifiers

PMID21421847
PMCPMC3090249

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.