Evidence map›Paper›PMID 16771853›Full record

ArticleImmunology2006

Effect of oestradiol on PAMP-mediated CCL20/MIP-3 alpha production by mouse uterine epithelial cells in culture.

Gisela Soboll, Mardi A Crane-Godreau, Magdalena A Lyimo, Charles R Wira

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Immunomodulatory Effects of 17Journal of immunology research · 2018
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. CCL20/MIP3alpha is a novel anti-HIV-1 molecule of the human female reproductive tract.American journal of reproductive immunology (New York, N.Y. : 1989) · 2009
    Article
  14. Article
  15. Article
  16. Article
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 1 institution in 1 country.

Gisela SobollDepartment of Physiology, Dartmouth Medical School, Lebanon, NH 03765, USA.
Mardi A Crane-Godreau
Magdalena A Lyimo
Charles R Wira
Dartmouth College · US

Funding

SEX HORMONE REGULATION OF THE MUCOSAL IMMUNE SYSTEMR37AI013541 · NIAID · DARTMOUTH COLLEGE · PI WIRA, CHARLES ROBERT · 1997 to 2005
$2.1M
SEX HORMONE REGULATION OF THE MUCOSAL IMMUNE SYSTEMR01AI013541 · NIAID · DARTMOUTH COLLEGE · PI WIRA, CHARLES ROBERT · 1985 to 2011
$2.0M
SEX HORMONE REGULATION OF THE MUCOSAL IMMUNE SYSTEMR55AI013541 · NIAID · DARTMOUTH COLLEGE · PI WIRA, CHARLES ROBERT · 1991 to 1991
–
NIAID NIH HHS AI-13541NIAID NIH HHS AI-33478NIAID NIH HHS R01 AI013541NIAID NIH HHS R37 AI013541
6 · The paper itself

Abstract

The present study was undertaken to establish whether mouse uterine epithelial cells produce CCL20/macrophage inflammatory protein 3 alpha (CCL20/MIP-3 alpha) and to determine whether secretion is under hormonal control and influenced by pathogen-associated molecular patterns (PAMPs). In the absence of PAMPs, polarized uterine epithelial cells grown to confluence on cell culture inserts constitutively secreted CCL20/MIP-3 alpha with preferential accumulation into the apical compartment. When epithelial cells were treated with the Toll-like receptor (TLR) agonists Pam3Cys (TLR2/1), peptidoglycan (TLR2/6) or lipopolysaccharide (LPS; TLR4), CCL20/MIP-3 alpha increased rapidly (4 hr) in both apical and basolateral secretions. Time-course studies indicated that responses to PAMPs added to the apical surface persisted for 12-72 hr. Stimulation with loxoribin (TLR7) and DNA CpG motif (TLR9) increased basolateral but not apical secretion of CCL20/MIP-3 alpha. In contrast, the viral agonist Poly(I:C) (TLR3) had no effect on either apical or basolateral secretion. In other studies, we found that oestradiol added to the culture media decreased the constitutive release of CCL20/MIP-3 alpha. Moreover, when added to the culture media along with LPS, oestradiol inhibited LPS-induced increases in CCL20/MIP-3 alpha secretion into both the apical and basolateral compartments. In summary, these results indicate that CCL20/MIP-3 alpha is produced in response to PAMPs. Since CCL20/MIP-3 alpha is chemotactic for immature dendritic cells, B cells and memory T cells and has antimicrobial properties, these studies suggest that CCL20/MIP-3 alpha production by epithelial cells, an important part of the innate immune defence in the female reproductive tract, is under hormonal control and is responsive to microbial challenge.

Indexed as

AnimalsCells, CulturedChemokine CCL20Chemokines, CCDipeptidesEpithelial CellsEstradiolFemaleGuanosineLipopolysaccharidesLipoproteinsMacrophage Inflammatory ProteinsMiceMice, Inbred BALB CPeptidoglycanToll-Like Receptors2,3-bis-(palmitoyloxy)-2-propyl-N-palmitoyl-cysteinylserineCCL20 protein, humanChemokine CCL20Chemokines, CCDipeptidesEstradiolGuanosineLipopolysaccharidesLipoproteinsloxoribineMacrophage Inflammatory ProteinsPeptidoglycanToll-Like Receptors

Identifiers

PMID16771853
PMCPMC1782293
OpenAlexW2127986325

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.