Evidence map›Paper›PMID 31191556›Full record

ArticleFrontiers in immunology2019

Human Monocyte-Derived Dendritic Cells Produce Millimolar Concentrations of ROS in Phagosomes Per Second.

Laurent M Paardekooper, Ilse Dingjan, Peter T A Linders, Alexander H J Staal, Simona M Cristescu, Wilco C E P Verberk, Geert van den Bogaart

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 63 citations in OpenAlex.

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  12. Disulfide-HMGB1 signals through TLR4 and TLR9 to induce inflammatory macrophages capable of innate-adaptive crosstalk in human liver transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 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

7 authors at 3 institutions in 1 country.

Laurent M PaardekooperTumor Immunology Lab, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Ilse DingjanTumor Immunology Lab, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Peter T A LindersTumor Immunology Lab, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Alexander H J StaalTumor Immunology Lab, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Simona M CristescuDepartment of Molecular and Laser Physics, Institute of Molecules and Materials, Radboud University, Nijmegen, Netherlands.
Wilco C E P VerberkAnimal Ecology and Ecophysiology, Institute for Water and Wetland Research, Radboud University, Nijmegen, Netherlands.
Geert van den BogaartTumor Immunology Lab, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
Radboud University Medical Center · NLRadboud University Nijmegen · NLPrincess Máxima Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils kill ingested pathogens by the so-called oxidative burst, where reactive oxygen species (ROS) are produced in the lumen of phagosomes at very high rates (mM/s), although these rates can only be maintained for a short period (minutes). In contrast, dendritic cells produce ROS at much lower rates, but they can sustain production for much longer after pathogen uptake (hours). It is becoming increasingly clear that this slow but prolonged ROS production is essential for antigen cross-presentation to activate cytolytic T cells, and for shaping the repertoire of antigen fragments for presentation to helper T cells. However, despite this importance of ROS production by dendritic cells for activation of the adaptive immune system, their actual ROS production rates have never been quantified. Here, we quantified ROS production in human monocyte-derived dendritic cells by measuring the oxygen consumption rate during phagocytosis. Although a large variation in oxygen consumption and phagocytic capacity was present among individuals and cells, we estimate a ROS production rate of on average ~0.5 mM/s per phagosome. Quantitative microscopy approaches showed that ROS is produced within minutes after pathogen encounter at the nascent phagocytic cup. H

Indexed as

AnimalsCells, CulturedCross-PrimingDendritic CellsFluoresceinsFluorescent DyesHumansKineticsLipopeptidesLipopolysaccharidesMiceMonocytesNADPH Oxidase 2Oxygen ConsumptionPhagosomesPhosphoproteins2',7'-dichlorodihydrofluorescein diacetateCYBB protein, humanFluoresceinsFluorescent DyesLipopeptideslipopolysaccharide, Escherichia coli O111 B4LipopolysaccharidesNADPH Oxidase 2neutrophil cytosol factor 67KPam(3)CSK(4) peptidePhosphoproteinsReactive Oxygen SpeciesSuperoxidesZymosandendritic cells (DCs)NOX2phagosomesquantitative biologyreactive oxygen species (ROS)

Identifiers

PMID31191556
PMCPMC6548834
OpenAlexW2947034940

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.