Evidence map›Paper›PMID 16171455›Full record

ArticleThe Biochemical journal2006

CD16b associates with high-density, detergent-resistant membranes in human neutrophils.

Maria J G Fernandes, Emmanuelle Rollet-Labelle, Guillaume Paré, Sébastien Marois, Marie-Lisane Tremblay, Jean-Luc Teillaud, Paul H Naccache

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

20 citing papers in PubMed, 44 citations in OpenAlex.

  1. Development of CRISPR/Cas9-mediated CD16bFrontiers in immunology · 2025
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  20. Profound functional and signaling changes in viable inflammatory neutrophils homing to cystic fibrosis airways.Proceedings of the National Academy of Sciences of the United States of America · 2008
    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

7 authors at 3 institutions in 2 countries.

Maria J G FernandesDepartment of Rheumatology and Immunology, CHUL Research Centre, Laval University, 2705 boulevarde Laurier, Sainte-Foy, Québec, Canada, G1V 4G2. maria.fernandes@crchul.ulaval.ca
Emmanuelle Rollet-Labelle
Guillaume Paré
Sébastien Marois
Marie-Lisane Tremblay
Jean-Luc Teillaud
Paul H Naccache
Université Laval · CAWilfrid Laurier University · CACentre de Recherche des Cordeliers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD16b is unique in that it is the only Fc receptor linked to the plasma membrane by a GPI (glycosylphosphatidylinositol) anchor. GPI-anchored proteins often preferentially localize to DRMs (detergent-resistant membranes) that are rich in sphingolipids and cholesterol and play an important role in signal transduction. Even though the responses to CD16b engagement have been intensively investigated, the importance of DRM integrity for CD16b signalling has not been characterized in human neutrophils. We provide direct evidence that CD16b constitutively partitions with both low- and high-density DRMs. Moreover, upon CD16b engagement, a significant increase in the amount of the receptor is observed in high-density DRMs. Similarly to CD16b, CD11b also resides in low- and high-density DRMs. In contrast with CD16b, the partitioning of CD11b in DRMs does not change in response to CD16b engagement. We also provide evidence for the implication of Syk in CD16b signalling and its partitioning to DRMs in resting and activated PMNs (polymorphonuclear neutrophils). Additionally, DRM-disrupting agents, such as nystatin and methyl-beta-cyclodextrin, alter cellular responses to CD16b receptor ligation. Notably, a significant increase in the mobilization of intracellular Ca2+ and in tyrosine phosphorylation of intracellular substrates after CD16b engagement is observed. Altogether, the results of this study provide evidence that high-density DRMs play a role in CD16b signalling in human neutrophils.

Indexed as

Antigens, CDbeta-CyclodextrinsCalciumCell MembraneGPI-Linked ProteinsHumansMacrophage-1 AntigenNeutrophilsNystatinProtein BindingReceptors, IgGSignal TransductionAntigens, CDbeta-CyclodextrinsbetadexCalciumFCGR3B protein, humanGPI-Linked ProteinsMacrophage-1 AntigenNystatinReceptors, IgG

Identifiers

PMID16171455
PMCPMC1383694
OpenAlexW2083111869

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.