Evidence map›Paper›PMID 26666685›Full record

ArticleNature communications2015

Natural cytotoxicity receptor splice variants orchestrate the distinct functions of human natural killer cell subtypes.

Johan Siewiera, Jordi Gouilly, Hocine-Rachid Hocine, Géraldine Cartron, Claude Levy, Reem Al-Daccak, Nabila Jabrane-Ferrat

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

67 citing papers in PubMed, 101 citations in OpenAlex.

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7 more citing papers are in PubMed but not listed here.

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 6 institutions in 1 country.

Johan SiewieraINSERM UMR 1043, Centre de Physiopathologie de Toulouse Purpan (CPTP), Toulouse F-31300, France.
Jordi GouillyINSERM UMR 1043, Centre de Physiopathologie de Toulouse Purpan (CPTP), Toulouse F-31300, France.
Hocine-Rachid HocineINSERM UMRS976 and Université Paris-Diderot, Hôpital Saint Louis, Paris 75010, France.
Géraldine CartronService de Gynécologie-Obstétrique, Centre Hospitalo-Universitaire de Toulouse, Hôpital Paule de Viguier, Toulouse 31059, France.
Claude LevyService de Gynécologie-Obstétrique Clinique Sarrus-Teinturiers, Toulouse 31300, France.
Reem Al-DaccakINSERM UMRS976 and Université Paris-Diderot, Hôpital Saint Louis, Paris 75010, France.
Nabila Jabrane-FerratINSERM UMR 1043, Centre de Physiopathologie de Toulouse Purpan (CPTP), Toulouse F-31300, France.
Hôpital Saint-Louis · FRCentre de Physiopathologie de Toulouse-Purpan · FRClinique Pasteur · FRHôpital Paule de Viguier · FRInserm · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The natural cytotoxicity receptors NKp46/NCR1, NKp44/NCR2 and NKp30/NCR3 are critical for natural killer (NK) cell functions. Their genes are transcribed into several splice variants whose physiological relevance is not yet fully understood. Here we report that decidua basalis NK (dNK) cells of the pregnant uterine mucosa and peripheral blood NK (pNK) cells, two functionally distinct subsets of the physiological NK cell pool, display differential expression of NKp30/NCR3 and NKp44/NCR2 splice variants. The presence of cytokines that are enriched within the decidual microenvironment is sufficient to convert the splice variant profile of pNK cells into one similar to that of dNK cells. This switch is associated with decreased cytotoxic function and major adaptations to the secretome, hallmarks of the decidual phenotype. Thus, NKp30/NCR3 and NKp44/NCR2 splice variants delineate functionally distinct NK cell subsets. To our knowledge, this is the first conclusive evidence underlining the physiological importance of NCR splice variants.

Indexed as

AdolescentAdultCytokinesDeciduaFemaleGene Expression RegulationHumansKiller Cells, NaturalPregnancyProtein IsoformsReceptors, Natural Cytotoxicity TriggeringYoung AdultCytokinesProtein IsoformsReceptors, Natural Cytotoxicity Triggering

Identifiers

PMID26666685
PMCPMC4682172
OpenAlexW2215776180

What OpenQuestion holds

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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.