Evidence map›Paper›PMID 23806179›Full record

ArticlePlacenta2013

Receptors for non-MHC ligands contribute to uterine natural killer cell activation during pregnancy in mice.

A M Felker, Z Chen, W G Foster, B A Croy

Abstract read
In one paragraph

Article in Placenta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. A Framework for Understanding Maternal Immunity.Immunology and allergy clinics of North America · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Cytokine-Based Generation of CD49aFrontiers in immunology · 2018
    Article
  13. Article
  14. Review
  15. Mapping out p38MAPK.American journal of reproductive immunology (New York, N.Y. : 1989) · 2017
    Review
  16. Review
  17. Review
  18. Article
  19. Composition, Development, and Function of Uterine Innate Lymphoid Cells.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  20. Leukocyte driven-decidual angiogenesis in early pregnancy.Cellular & molecular immunology · 2014
    Review
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

4 authors at 2 institutions in 1 country.

A M FelkerDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, ON, Canada K7L3N6.
Z Chen
W G Foster
B A Croy
Queen's University · CAMcMaster University · CA

Funding

CIHR 77519-2
6 · The paper itself

Abstract

introductionActivated uterine natural killer (uNK) cells are abundant in early human and mouse decidual basalis. In mice, distinct uNK cell subsets support early endothelial tip cell induction, the pruning of new vessels and initiation of spiral arterial modification. While genetic studies indicate that NK/uNK cell activation via receptors recognizing Class I MHC-derived peptides promotes human pregnancy, roles for other activation receptors expressed by NK cells, such as the aryl hydrocarbon receptor (AHR) and natural cytotoxicity receptors (NCR) are undefined in human or mouse pregnancies.

methodsExpression of AHR and NCR1 (ortholog of human NKp46) by gestation day (gd)10.5 mouse uNK cell subsets was measured by quantitative real-time RT-PCR. Early implantation sites from mice lacking expression of either receptor were examined histologically.

resultsGd10.5 uNK cell subsets, separated by reactivity to Dolichos biflorus agglutinin lectin, differed in relative transcript abundance for Ahr and Ncr1. Quantitative histology revealed that, in comparison to C57BL/6 controls, implant sites from gd10.5 Ahr(-/-) and gd6.5-12.5 UkCa:B6.Ncr1(Gfp/Gfp) mice had normal uNK cell abundance but the uNK cells were smaller than normal and unable to trigger spiral arterial remodeling. Whole mount immunohistochemistry comparisons of viable, gd6.5-8.5 Ncr1(Gfp/Gfp) and C57BL/6 implant sites revealed deficits in implant site angiogenesis and conceptus growth in Ncr1(Gfp/Gfp). DISCUSSION: In mice, activation of AHR and of NCR1 by endogenous, as yet undefined ligands, contributes to uNK cell activation/maturation and angiogenic functions during early to mid-gestation pregnancy. MHC-independent activation of uNK cells also likely makes critical contributions to human pregnancy success.

Indexed as

Gene Expression Regulation, DevelopmentalLymphocyte ActivationAgglutininsAnimalsAntigens, LyBasic Helix-Loop-Helix ProteinsDeciduaEmbryo ImplantationFemaleKiller Cells, NaturalLeukopoiesisLigandsMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicAgglutininsAhr protein, mouseAntigens, LyBasic Helix-Loop-Helix Proteinsdolichos biflorus agglutininLigandsNatural Cytotoxicity Triggering Receptor 1Ncr1 protein, mousePlant LectinsReceptors, Aryl HydrocarbonArylhydrocarbon receptorDeciduaHistologyNatural cytotoxicity receptorReproductive immunologySpiral artery remodeling

Identifiers

PMID23806179
PMCPMC3742434
OpenAlexW2069911190

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.