Evidence map›Paper›PMID 12748293›Full record

ArticleMolecular and cellular biology2003

Interleukin-13 induction of 15-lipoxygenase gene expression requires p38 mitogen-activated protein kinase-mediated serine 727 phosphorylation of Stat1 and Stat3.

Bo Xu, Ashish Bhattacharjee, Biswajit Roy, Hong-Min Xu, David Anthony, David A Frank, Gerald M Feldman, Martha K Cathcart

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Sensitization of colonic nociceptors by IL-13 is dependent on JAK and p38 MAPK activity.American journal of physiology. Gastrointestinal and liver physiology · 2023
    Article
  6. Review
  7. Surfactant Protein-A Protects against IL-13-Induced Inflammation in Asthma.Journal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Global discovery of high-NaCl-induced changes of protein phosphorylation.American journal of physiology. Cell physiology · 2014
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. p38α and p38β mitogen-activated protein kinases determine cholinergic transdifferentiation of sympathetic neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    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

8 authors at 3 institutions in 1 country.

Bo XuDepartment of Cell Biology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
Ashish Bhattacharjee
Biswajit Roy
Hong-Min Xu
David Anthony
David A Frank
Gerald M Feldman
Martha K Cathcart
Cleveland Clinic · USCenter for Biologics Evaluation and Research · USDana-Farber Cancer Institute · US

Funding

MONOCYTE OXIDATION OF LIPOPROTEIN LIPIDSR01HL051068 · NHLBI · CLEVELAND CLINIC FOUNDATION · PI CATHCART, MARTHA K · 1995 to 2002
$778k
NHLBI NIH HHS HL51068
6 · The paper itself

Abstract

Interleukin-13 (IL-13) is a cytokine secreted by Th2 lymphocytes that is capable of inducing expression of 15-lipoxygenase (15-LO) in primary human monocytes. We recently demonstrated that induction of 15-LO requires the activation of Jak2 and Tyk2 kinases and Stats 1, 3, 5, and 6. Since IL-13-induced 15-LO expression was inhibited by H7 (a serine-threonine kinase inhibitor), we predicted that Stat serine phosphorylation may also be crucial for 15-LO expression. In this study, we present evidence indicating that IL-13-induced 15-LO mRNA expression was detectable as early as 1 h by real-time reverse transcription-PCR. We found that IL-13 induced a time-dependent serine phosphorylation of both Stat1 and Stat3, detectable at 15 min after IL-13 treatment. In addition, the activation of p38 mitogen-activated protein kinase (MAPK) was detected in a time-dependent fashion, with peak phosphorylation at 15 min after IL-13 treatment. SB202190, a p38 MAPK-specific inhibitor, markedly inhibited IL-13-induced Stat1 and Stat3 serine phosphorylation as well as DNA binding. Furthermore, treatment of cells with Stat1 or Stat3 decoys significantly impaired IL-13-induced 15-LO expression. Taken together, our results provide the first evidence that IL-13 induces p38 MAPK phosphorylation/activation, which regulates Stat1 and Stat3 serine 727 phosphorylation. Both of these events are important steps in IL-13-induced 15-LO expression in human monocytes.

Indexed as

Gene Expression RegulationAnimalsArachidonate 15-LipoxygenaseCells, CulturedDNADNA-Binding ProteinsEnzyme InhibitorsHumansInterleukin-13Mitogen-Activated Protein KinasesMonocytesp38 Mitogen-Activated Protein KinasesPhosphorylationSerineSignal TransductionSTAT1 Transcription FactorArachidonate 15-LipoxygenaseDNADNA-Binding ProteinsEnzyme InhibitorsInterleukin-13Mitogen-Activated Protein Kinasesp38 Mitogen-Activated Protein KinasesSerineSTAT1 protein, humanSTAT1 Transcription FactorSTAT3 protein, humanSTAT3 Transcription FactorTrans-Activators

Identifiers

PMID12748293
PMCPMC155212
OpenAlexW2129217778

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Registered trials

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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.