Evidence map›Paper›PMID 17588655›Full record

ArticlePlacenta2007

Cell type-specific expression and function of toll-like receptors 2 and 4 in human placenta: implications in fetal infection.

Y Ma, G Krikun, V M Abrahams, G Mor, S Guller

Open access · greenAbstract read
In one paragraph

Article in Placenta, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 90 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Article
  7. The Immunology of Syncytialized Trophoblast.International journal of molecular sciences · 2021
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
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  17. Review
  18. Article
  19. Do the placental barrier, parasite genotype and Toll-like receptor polymorphisms contribute to the course of primary infection with various Toxoplasma gondii genotypes in pregnant women?European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2014
    Review
  20. Viral infection, inflammation and schizophrenia.Progress in neuro-psychopharmacology & biological psychiatry · 2013
    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

5 authors at 1 institution in 1 country.

Y MaDepartment of Obstetrics/Gynecology and Reproductive Sciences, Yale University School of Medicine, 333 Cedar Street-339 FMB, PO Box 208063, New Haven, CT 06520-8063, USA.
G Krikun
V M Abrahams
G Mor
S Guller
Yale University · US

Funding

Targeting Placental Pathophysiology in IUGR and PreeclampsiaR01HD033909 · NICHD · YALE UNIVERSITY · PI GULLER, SETH M. · 2002 to 2010
$2.5M
Targeting Placental Pathophysiology in IUGR and PreeclampsiaR56HD033909 · NICHD · YALE UNIVERSITY · PI GULLER, SETH M. · 2008 to 2008
$317k
GLUCOCORTICOIDS AND MATRIX PROTEINS AT PARTURITIONR29HD033909 · NICHD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GULLER, SETH · 1995 to 1999
–
NICHD NIH HHS HD33909NICHD NIH HHS R01 HD033909NICHD NIH HHS R29 HD033909NICHD NIH HHS R56 HD033909
6 · The paper itself

Abstract

Placental infection is associated with adverse fetal outcomes. Toll-like receptors (TLRs) are critical regulators of the innate immune response based on their ability to recognize and respond to pathogen-associated molecular patterns expressed by microbes. To date, cell-type specific expression and regulation of TLR function in human term placenta remains largely unelucidated. The goal of the current study was to examine the in vivo and in vitro patterns of TLR expression and function in major cell types of term placenta. Immunohistochemical analysis of terminal and stem villi localized TLR-2, which recognizes peptidoglycan (PG) from Gram-positive bacteria, to endothelial cells and macrophages, and to a lesser extent to syncytiotrophoblast (SCTs) and fibroblasts (FIBs). Staining for TLR-4, the receptor for Gram-negative bacterial lipopolysaccharide (LPS), was most prominent in SCTs and endothelial cells. Results from Western blotting, conventional, and quantitative PCR (qRTPCR) analyses using protein and mRNA isolated from cultures of SCTs and myofibroblasts (mFIBs) revealed that SCTs expressed TLR-2 and TLR-4, whereas mFIBs expressed only TLR-4. In addition, qRTPCR showed that LPS treatment increased TLR-2 expression in SCTs, indicating that infection with Gram-negative bacteria may enhance innate immune responses in placenta toward a broad range of microorganisms. In addition, treatment with LPS increased IL-8 levels in both SCTs and mFIBs, whereas PG treatment only stimulated IL-8 levels in SCTs. Our results indicate that there exist cell type-specific patterns of TLR function in placenta which likely regulate innate immune response at the maternal-fetal interface.

Indexed as

Cells, CulturedFemaleFetal DiseasesFibroblastsHumansLipopolysaccharidesPeptidoglycanPlacentaPlacenta DiseasesPregnancyPregnancy Complications, InfectiousToll-Like Receptor 2Toll-Like Receptor 4TrophoblastsLipopolysaccharidesPeptidoglycanTLR2 protein, humanTLR4 protein, humanToll-Like Receptor 2Toll-Like Receptor 4

Identifiers

PMID17588655
PMCPMC2064901
OpenAlexW2094761218

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.