Evidence map›Paper›PMID 16920968›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2006

The roles of bacteria and TLR4 in rat and murine models of necrotizing enterocolitis.

Tamas Jilling, Dyan Simon, Jing Lu, Fan Jing Meng, Dan Li, Robert Schy, Richard B Thomson, Antoine Soliman, Moshe Arditi, Michael S Caplan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 245 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
245citing papers in PubMed, 3 pooled it
9.8field-weighted citation impact, top 1% 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

245 citing papers in PubMed, 3 syntheses or guidelines pooled it, 396 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Review
  7. Necrotizing enterocolitis.Nature reviews. Disease primers · 2026
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Necrotizing enterocolitis causes increased ileal goblet cell loss inbioRxiv : the preprint server for biology · 2025
    Article
  20. Article

185 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

10 authors at 3 institutions in 1 country.

Tamas JillingDepartment of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL 60614, USA.
Dyan Simon
Jing Lu
Fan Jing Meng
Dan Li
Robert Schy
Richard B Thomson
Antoine Soliman
Moshe Arditi
Michael S Caplan
Northwestern University · USNorthShore University HealthSystem · USCedars-Sinai Medical Center · US

Funding

THE ROLE OF PAF IN NEONATAL-NECROTIZING ENTEROCOLITISR01HD037581 · NICHD · NORTHSHORE UNIV HEALTHSYSTEM RES INST · PI CAPLAN, MICHAEL S · 2000 to 2010
$2.6M
MD2 signaling in LPS/TLR4 induced cellular responsesR01AI058128 · NIAID · CEDARS-SINAI MEDICAL CENTER · PI ARDITI, MOSHE · 2004 to 2009
$2.4M
PAF Receptor Trafficking and Function in Epithelial CellsR01DK062960 · NIDDK · NORTHSHORE UNIVERSITY HEALTHSYSTEM · PI JILLING, TAMAS SANDOR · 2006 to 2010
$1.2M
NIAID NIH HHS R01 AI058128NICHD NIH HHS R01 HD037581NICHD NIH HHS R01 HD37581NIDDK NIH HHS R01 DK062960
6 · The paper itself

Abstract

Bacteria are thought to contribute to the pathogenesis of necrotizing enterocolitis (NEC), but it is unknown whether their interaction with the epithelium can participate in the initiation of mucosal injury or they can act only following translocation across a damaged intestinal barrier. Our aims were to determine whether bacteria and intestinal epithelial TLR4 play roles in a well-established neonatal rat model and a novel neonatal murine model of NEC. Neonatal rats, C57BL/6J, C3HeB/FeJ (TLR4 wild type), and C3H/HeJ (TLR4 mutant) mice were delivered by Cesarean section and were subjected to formula feeding and cold asphyxia stress or were delivered naturally and were mother-fed. NEC incidence was evaluated by histological scoring, and gene expression was quantified using quantitative real-time PCR from cDNA generated from intestinal total RNA or from RNA obtained by laser capture microdissection. Spontaneous feeding catheter colonization or supplementation of cultured bacterial isolates to formula increased the incidence of experimental NEC. During the first 72 h of life, i.e., the time frame of NEC development in this model, intestinal TLR4 mRNA gradually decreases in mother-fed but increases in formula feeding and cold asphyxia stress, correlating with induced inducible NO synthase. TLR4, inducible NO synthase, and inflammatory cytokine induction occurred in the intestinal epithelium but not in the submucosa. NEC incidence was diminished in C3H/HeJ mice, compared with C3HeB/FeJ mice. In summary, bacteria and TLR4 play significant roles in experimental NEC, likely via an interaction of intraluminal bacteria and aberrantly overexpressed TLR4 in enterocytes.

Indexed as

Animal FeedAnimalsAsphyxiaChemokines, CXCChorionic VilliDisease Models, AnimalEnterocolitis, NecrotizingEpitheliumGene ExpressionMiceMutationNitric Oxide Synthase Type IIRatsRNA, MessengerToll-Like Receptor 4Up-RegulationChemokines, CXCNitric Oxide Synthase Type IIRNA, MessengerTlr4 protein, mouseTlr4 protein, ratToll-Like Receptor 4

Identifiers

PMID16920968
PMCPMC2697969
OpenAlexW2163194273

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.