Evidence map›Paper›PMID 27249817›Full record

ArticleOpen biology2016

Modulation of natural killer cell functions by interactions between 2B4 and CD48 in cis and in trans.

Maren Claus, Sabine Wingert, Carsten Watzl

Open access · goldAbstract read
In one paragraph

Article in Open biology, 2016. 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
0.8field-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

15 citing papers in PubMed, 22 citations in OpenAlex.

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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

3 authors at 1 institution in 2 countries.

Maren ClausLeibniz Research Centre for Working Environment and Human Factors at TU Dortmund (IfADo) Dortmund, Germany.
Sabine WingertLeibniz Research Centre for Working Environment and Human Factors at TU Dortmund (IfADo) Dortmund, Germany.
Carsten WatzlLeibniz Research Centre for Working Environment and Human Factors at TU Dortmund (IfADo) Dortmund, Germany watzl@ifado.de.ORCID 0000-0001-5195-0995
Google (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SLAM-related receptors (SRRs) are important modulators of immune cell function. While most SRRs are homophilic, 2B4 (CD244) interacts with CD48, a GPI-anchored protein expressed on many haematopoietic cells. Here we show that natural killer (NK) cell-expressed 2B4 not only binds in trans to CD48 on neighbouring cells but also interacts in cis with CD48 on the same cell. 2B4 uses the same binding site to interact with CD48 in cis and in trans and structural flexibility of 2B4 is necessary for the cis interaction. Furthermore, the cis interaction is sufficient to induce basal phosphorylation of 2B4. However, cis interaction reduces the ability of 2B4 to bind CD48 in trans As a consequence, stimulation-dependent phosphorylation of 2B4 upon binding to CD48 positive target cells is reduced. Interfering with the cis interaction therefore enhanced the lysis of CD48-expressing tumour cells. These data show that the density of 2B4 and CD48 on both the NK cell and the potential target cell modulates NK cell activity.

Indexed as

Binding SitesCD48 AntigenCoculture TechniquesHEK293 CellsHumansJurkat CellsKiller Cells, NaturalPhosphorylationProtein BindingSignaling Lymphocytic Activation Molecule FamilyCD244 protein, humanCD48 AntigenCD48 protein, humanSignaling Lymphocytic Activation Molecule Family2B4CD48cytotoxicitynatural killer cellssurface receptors

Identifiers

PMID27249817
PMCPMC4892432
OpenAlexW2403928379

What OpenQuestion holds

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LicenceCC BY
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.