Evidence map›Paper›PMID 17709515›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2007

NF-kappaB signaling regulates functional expression of the MHC class I-related neonatal Fc receptor for IgG via intronic binding sequences.

Xindong Liu, Lilin Ye, Gregory J Christianson, Jun-Qi Yang, Derry C Roopenian, Xiaoping Zhu

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

60 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
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  5. Article
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  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. The therapeutic age of the neonatal Fc receptor.Nature reviews. Immunology · 2023
    Review
  13. Dysfunction of Foxp3International journal of molecular sciences · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. In Translation: FcRn across the Therapeutic Spectrum.International journal of molecular sciences · 2021
    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

6 authors at 3 institutions in 1 country.

Xindong LiuLaboratory of Immunology, Virginia-Maryland Regional College of Veterinary Medicine, University of Maryland, 8075 Greenmead Drive, College Park, MD 20742, USA.
Lilin Ye
Gregory J Christianson
Jun-Qi Yang
Derry C Roopenian
Xiaoping Zhu
Virginia–Maryland College of Veterinary Medicine · USJackson Laboratory · USUniversity of Cincinnati Medical Center · US

Funding

CLASS I MOLECULES AND AUTOIMMUNITYR01DK056597 · NIDDK · JACKSON LABORATORY · PI ROOPENIAN, DERRY CHARLES · 1999 to 2006
$2.4M
Transcytosis of IgG in Genital InfectionsR01AI065892 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI ZHU, XIAOPING · 2007 to 2010
$1.2M
AIDS Vaccine Strategy Using IgG Transfer PathwayR21AI073139 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI ZHU, XIAOPING · 2007 to 2008
$398k
Immunogenicity of Subunit Vaccine Delivered by FcRnR21AI067965 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI ZHU, XIAOPING · 2006 to 2007
$393k
NIAID NIH HHS AI 65892NIAID NIH HHS AI 67965NIAID NIH HHS R01 AI065892NIAID NIH HHS R21 AI067965NIAID NIH HHS R21 AI073139NIDDK NIH HHS R01 DK056597
6 · The paper itself

Abstract

The neonatal Fc receptor for IgG (FcRn) functions to transport maternal IgG to a fetus or newborn and to protect IgG from degradation. Although FcRn is expressed in a variety of tissues and cell types, the extent to which FcRn expression is regulated by immunological and inflammatory events remains unknown. Stimulation of intestinal epithelial cell lines, macrophage-like THP-1, and freshly isolated human monocytes with the cytokine TNF-alpha rapidly up-regulated FcRn gene expression. In addition, the TLR ligands LPS and CpG oligodeoxynucleotide enhanced the level of FcRn expression in THP-1 and monocytes. Treatment of TNF-stimulated THP-1 cells with the NF-kappaB-specific inhibitor or overexpression of a dominant negative mutant inhibitory NF-kappaB (IkappaBalpha; S32A/S36A) resulted in down-regulation of FcRn expression. By using chromatin immunoprecipitation we identified three NF-kappaB binding sequences within introns 2 and 4 of the human FcRn gene. An EMSA confirmed the p50/p50 and/or p65/p50 complex (s) bound to intron 2- or 4-derived oligonucleotides containing putative NF-kappaB binding sequences, respectively. The intronic NF-kappaB sequences in combination with the promoter or alone regulated the expression of a luciferase reporter gene in response to TNF-alpha stimulation or overexpression of NF-kappaB p65 and p50. DNA looping interactions potentially occurred after the stimulation between intronic NF-kappaB sequences and the FcRn promoter as shown by a chromosome conformation capture assay. Finally, TNF-alpha stimulations enhanced IgG transport across an intestinal Caco-2 epithelial monolayer. Together, these data provide the first evidence that NF-kappaB signaling via intronic sequences regulates FcRn expression and function.

Indexed as

Gene Expression RegulationIntronsBase SequenceBinding SitesCaco-2 CellsGene ExpressionHistocompatibility Antigens Class IHumansImmunoglobulin GInterleukin-1betaIntestinal MucosaLuciferasesNF-kappa BPromoter Regions, GeneticProtein TransportReceptors, FcFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GInterleukin-1betaLuciferasesNF-kappa BReceptors, FcReceptors, IgGTumor Necrosis Factor-alpha

Identifiers

PMID17709515
PMCPMC2667116
OpenAlexW1555726473

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.