Evidence map›Paper›PMID 20181890›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

The septic shock-associated IL-10 -1082 A > G polymorphism mediates allele-specific transcription via poly(ADP-Ribose) polymerase 1 in macrophages engulfing apoptotic cells.

Xiaoyan Kang, Ha-Jeong Kim, Michelle Ramirez, Sarah Salameh, Xiaojing Ma

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Biomedicines · 2022
    Article
  6. Review
  7. Review
  8. Bhlhe40 is an essential repressor of IL-10 duringThe Journal of experimental medicine · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Regulation of interleukin-10 gene expression in macrophages engulfing apoptotic cells.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2010
    Review
  20. 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 3 institutions in 2 countries.

Xiaoyan KangDepartment of Microbiology and Immunology, Weill Cornell Medical College, Cornell University, New York, NY 10065, USA.
Ha-Jeong Kim
Michelle Ramirez
Sarah Salameh
Xiaojing Ma
Cornell University · USNewYork–Presbyterian Hospital · USWeill Cornell Medical College in Qatar · QA

Funding

MECHANISMS OF INHIBITION OF IL 12 PRODUCTIONR01AI045899 · NIAID · WISTAR INSTITUTE · PI MA, XIAOJING · 1999 to 2008
$2.8M
NIAID NIH HHS R01 AI045899
6 · The paper itself

Abstract

The biallelic IL-10 single nucleotide polymorphism at -1082 of the promoter region linked to individual variation in cytokine inducibility has been strongly implicated in several pathological conditions including the development of, and outcomes in, septic shock during pneumococcal infection, acute respiratory distress syndrome, and cardiac dysfunction. However, the molecular basis of the single nucleotide polymorphism-mediated variable IL-10 production levels has not been explored. In this study, we report that the -1082G > A alleles in the promoter region of the human IL-10 gene physically interact with a nuclear protein in an allele-specific manner that results in different levels of IL-10 transcription. This protein has been identified as poly(ADP-ribose) polymerase 1 (PARP-1). We show that PARP-1 acts as a transcription repressor, and its DNA-binding activity is strongly regulated in macrophages that engulf apoptotic cells but not stimulated with LPS. These findings unveil a novel role of PARP-1 in the regulation of IL-10 production in an allele-dependent way, which determines individual susceptibility to sepsis-induced inflammatory pathology and the immunological sequelae in a physiological process in which clearance of infection-induced apoptotic cells by professional phagocytes triggers the cytokine synthesis.

Indexed as

AllelesAnimalsApoptosisElectrophoresis, Polyacrylamide GelElectrophoretic Mobility Shift AssayGenetic Predisposition to DiseaseHumansInterleukin-10Jurkat CellsMacrophagesMiceOligonucleotide Array Sequence AnalysisPhagocytosisPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesPolymorphism, Single NucleotideInterleukin-10PARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerases

Identifiers

PMID20181890
PMCPMC3637664
OpenAlexW1566936870

What OpenQuestion holds

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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.