Evidence map›Paper›PMID 30808727›Full record

ArticleMolecular & cellular proteomics : MCP2019

Spatiotemporal Changes of the Phagosomal Proteome in Dendritic Cells in Response to LPS Stimulation.

Anne-Marie Pauwels, Anetta Härtlova, Julien Peltier, Yasmine Driege, Griet Baudelet, Priscille Brodin, Matthias Trost, Rudi Beyaert, Eik Hoffmann

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

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  6. Assessing the Phagosome Proteome by Quantitative Mass Spectrometry.Methods in molecular biology (Clifton, N.J.) · 2023
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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 at 5 institutions in 3 countries.

Anne-Marie PauwelsFrom the ‡Unit of Molecular Signal Transduction in Inflammation, VIB Center for Inflammation Research, Ghent, Belgium;; §Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Anetta Härtlova¶Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle-upon-Tyne, UK.
Julien Peltier¶Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle-upon-Tyne, UK.
Yasmine DriegeFrom the ‡Unit of Molecular Signal Transduction in Inflammation, VIB Center for Inflammation Research, Ghent, Belgium;; §Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Griet BaudeletFrom the ‡Unit of Molecular Signal Transduction in Inflammation, VIB Center for Inflammation Research, Ghent, Belgium;; §Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Priscille Brodin‖Univ. Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-CIIL-Center for Infection and Immunity of Lille, Lille, France.
Matthias Trost¶Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle-upon-Tyne, UK.
Rudi BeyaertFrom the ‡Unit of Molecular Signal Transduction in Inflammation, VIB Center for Inflammation Research, Ghent, Belgium;; §Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Eik HoffmannFrom the ‡Unit of Molecular Signal Transduction in Inflammation, VIB Center for Inflammation Research, Ghent, Belgium;; §Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium;; ‖Univ. Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-CIIL-Center for Infection and Immunity of Lille, Lille, France.
Newcastle University · GBVIB-UGent Center for Inflammation Research · BECentre National de la Recherche Scientifique · FRGhent University · BEUniversité de Lille · FR

Funding

Medical Research Council MC_UP_A500_1020Medical Research Council MC_UU_12016/5
6 · The paper itself

Abstract

Dendritic cells (DCs) are professional phagocytes that use innate sensing and phagocytosis to internalize and degrade self as well as foreign material, such as pathogenic bacteria, within phagosomes. These intracellular compartments are equipped to generate antigenic peptides that serve as source for antigen presentation to T cells initiating adaptive immune responses. The phagosomal proteome of DCs is only partially studied and is highly dynamic as it changes during phagosome maturation, when phagosomes sequentially interact with endosomes and lysosomes. In addition, the activation status of the phagocyte can modulate the phagosomal composition and is able to shape phagosomal functions.In this study, we determined spatiotemporal changes of the proteome of DC phagosomes during their maturation and compared resting and lipopolysaccharide (LPS)-stimulated bone marrow-derived DCs by label-free, quantitative mass spectrometry. Ovalbumin-coupled latex beads were used as phagocytosis model system and revealed that LPS-treated DCs show decreased recruitment of proteins involved in phagosome maturation, such as subunits of the vacuolar proton ATPase, cathepsin B, D, S, and RAB7. In contrast, those phagosomes were characterized by an increased recruitment of proteins involved in antigen cross-presentation,

Indexed as

AnimalsDendritic CellsKineticsLipopolysaccharidesMice, Inbred C57BLPhagosomesProteomeProteomicsTime FactorsLipopolysaccharidesProteomeCell biology*Cellular organelles*dendritic cellEndocytosis*Immunology*Inflammatory responseLabel-free quantificationphagocytosisphagosome maturationProtein Identification*

Identifiers

PMID30808727
PMCPMC6495253
OpenAlexW2916484398

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.