Evidence map›Paper›PMID 25847241›Full record

ArticleThe Journal of biological chemistry2015

Th2 Cytokines Augment IL-31/IL-31RA Interactions via STAT6-dependent IL-31RA Expression.

Ramakrishna Edukulla, Brijendra Singh, Anil G Jegga, Vishwaraj Sontake, Stacey R Dillon, Satish K Madala

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
3.8field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 47 citations in OpenAlex.

  1. IL-31: State of the Art for an Inflammation-Oriented Interleukin.International journal of molecular sciences · 2022
    Pooled it
  2. IL-33/IL-31 Axis in Immune-Mediated and Allergic Diseases.International journal of molecular sciences · 2019
    Pooled it
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Interleukin-31 and Pruritic Skin.Journal of clinical medicine · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. IL-31 induces antitumor immunity in breast carcinoma.Journal for immunotherapy of cancer · 2020
    Article
  15. IL-33/IL-31 Axis in Osteoporosis.International journal of molecular sciences · 2020
    Review
  16. Article
  17. A Phytocomplex Consisting ofOxidative medicine and cellular longevity · 2020
    Article
  18. Article
  19. Article
  20. 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

6 authors at 3 institutions in 1 country.

Ramakrishna EdukullaFrom the Divisions of Pulmonary Medicine and.
Brijendra SinghFrom the Divisions of Pulmonary Medicine and.
Anil G JeggaBiomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229 and.
Vishwaraj SontakeFrom the Divisions of Pulmonary Medicine and.
Stacey R Dillonthe ZymoGenetics, Inc. (a Bristol-Myers Squibb Company), Seattle, Washington 98102.
Satish K MadalaFrom the Divisions of Pulmonary Medicine and satish.madala@cchmc.org.
Pulmonary Associates · USBristol-Myers Squibb (United States) · USCincinnati Children's Hospital Medical Center · US

Funding

THE ROLE OF IL-31 IN TH2 CYTOKINE-DRIVEN SYSTEMIC SCLEROSISR03AR062832 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI MADALA, SATISH K · 2013 to 2015
$230k
NIAMS NIH HHS 1R03AR062832NIAMS NIH HHS R03 AR062832
6 · The paper itself

Abstract

Interleukin 31 receptor α (IL-31RA) is a novel Type I cytokine receptor that pairs with oncostatin M receptor to mediate IL-31 signaling. Binding of IL-31 to its receptor results in the phosphorylation and activation of STATs, MAPK, and JNK signaling pathways. IL-31 plays a pathogenic role in tissue inflammation, particularly in allergic diseases. Recent studies demonstrate IL-31RA expression and signaling in non-hematopoietic cells, but this receptor is poorly studied in immune cells. Macrophages are key immune-effector cells that play a critical role in Th2-cytokine-mediated allergic diseases. Here, we demonstrate that Th2 cytokines IL-4 and IL-13 are capable of up-regulating IL-31RA expression on both peritoneal and bone marrow-derived macrophages from mice. Our data also demonstrate that IL-4Rα-driven IL-31RA expression is STAT6 dependent in macrophages. Notably, the inflammation-associated genes Fizz1 and serum amyloid A (SAA) are significantly up-regulated in M2 macrophages stimulated with IL-31, but not in IL-4 receptor-deficient macrophages. Furthermore, the absence of Type II IL-4 receptor signaling is sufficient to attenuate the expression of IL-31RA in vivo during allergic asthma induced by soluble egg antigen, which may suggest a role for IL-31 signaling in Th2 cytokine-driven inflammation and allergic responses. Our study reveals an important counter-regulatory role between Th2 cytokine and IL-31 signaling involved in allergic diseases.

Indexed as

Gene Expression RegulationAnimalsAsthmaBlotting, WesternCells, CulturedChromatin ImmunoprecipitationFlow CytometryFluorescent Antibody TechniqueInflammationInterleukin-13Interleukin-4InterleukinsMacrophagesMiceMice, Inbred BALB CMice, Inbred C57BLIl31ra protein, mouseInterleukin-13interleukin-31, mouseInterleukin-4InterleukinsReceptors, InterleukinRNA, MessengerStat6 protein, mouseSTAT6 Transcription Factorallergic asthmaasthmacytokineinflammationinterleukin-31macrophagesignalingSTAT6Th2 cytokines

Identifiers

PMID25847241
PMCPMC4505597
OpenAlexW2057056528

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.