Evidence map›Paper›PMID 20432238›Full record

ArticleEuropean journal of immunology2010

Ligand dimensions are important in controlling NK-cell responses.

Joanna Brzostek, Jian-Guo Chai, Friedemann Gebhardt, Dirk H Busch, Rui Zhao, P Anton van der Merwe, Keith G Gould

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 20 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

7 authors at 4 institutions in 2 countries.

Joanna BrzostekDepartment of Immunology, Wright-Fleming Institute, Imperial College London, London, UK.
Jian-Guo Chai
Friedemann Gebhardt
Dirk H Busch
Rui Zhao
P Anton van der Merwe
Keith G Gould
Imperial College London · GBInstitute of Medical Microbiology and Hygiene · DEBabraham Institute · GBUniversity of Oxford · GB

Funding

Biotechnology and Biological Sciences Research Council BB/D011663/1Medical Research Council G19/31Medical Research Council G9722488Wellcome Trust
6 · The paper itself

Abstract

Size-dependent protein segregation at the cell-cell contact interface has been suggested to be critical for regulation of lymphocyte function. We investigated the role of ligand dimensions in regulation of mouse NK-cell activation and inhibition. Elongated forms of H60a, a mouse NKG2D ligand, were generated and expressed stably in the RMA cell line. RMA cells expressing the normal size H60a were lysed efficiently by both freshly isolated and IL-2 stimulated C57BL/6 mouse-derived NK cells; however the level of lysis decreased as the H60a ligand size increased. Importantly, H60a elongation did not affect NKG2D binding, as determined by soluble NKG2D tetramer staining, and by examining NK-cell target cell conjugate formation. CHO cells are efficient at activating NK cells from C57BL/6 mice, and expression of a single chain form of H-2K(b), a ligand for the mouse inhibitory receptor Ly49C, strongly inhibited such activation of Ly49C/I positive NK cells. Elongation of H-2K(b) resulted in decreased inhibition of both lysis and IFN-gamma production by NK cells. These results establish that small ligand dimensions are important for both NK-cell activation and inhibition, and suggest that there are shared features between the mechanisms of receptor triggering on different types of lymphocytes.

Indexed as

AnimalsCell Line, TumorCHO CellsCricetinaeCricetulusCytotoxicity, ImmunologicH-2 AntigensKiller Cells, NaturalLigandsMiceMice, Inbred C57BLMinor Histocompatibility AntigensMutagenesis, InsertionalMutagenesis, Site-DirectedNK Cell Lectin-Like Receptor Subfamily ANK Cell Lectin-Like Receptor Subfamily KH-2 AntigensH-2Kb protein, mouseKlrk1 protein, mouseLigandsminor H antigen H60Minor Histocompatibility AntigensNK Cell Lectin-Like Receptor Subfamily ANK Cell Lectin-Like Receptor Subfamily K

Identifiers

PMID20432238
PMCPMC2909396
OpenAlexW2070346468

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.