Evidence map›Paper›PMID 12813022›Full record

ArticleThe Journal of clinical investigation2003

Dissection of experimental asthma with DNA microarray analysis identifies arginase in asthma pathogenesis.

Nives Zimmermann, Nina E King, Johanne Laporte, Ming Yang, Anil Mishra, Sam M Pope, Emily E Muntel, David P Witte, Anthony A Pegg, Paul S Foster and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 190 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
190citing papers in PubMed, 4 pooled it
21.9field-weighted citation impact, top 1% 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

190 citing papers in PubMed, 4 syntheses or guidelines pooled it, 457 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Amino acid metabolism in health and disease.Signal transduction and targeted therapy · 2023
    Review
  13. Review
  14. M-MDSCFrontiers in immunology · 2023
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

130 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 3 countries.

Nives ZimmermannDivision of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.
Nina E King
Johanne Laporte
Ming Yang
Anil Mishra
Sam M Pope
Emily E Muntel
David P Witte
Anthony A Pegg
Paul S Foster
Qutayba Hamid
Marc E Rothenberg
Cincinnati Children's Hospital Medical Center · USAustralian National University · AUMcGill University · CA

Funding

REGULATION OF GASTROINTESTINAL EOSINOPHILSR01AI045898 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI ROTHENBERG, MARC E. · 1999 to 2024
$4.5M
Regulation of Gastrointestinal EosinophilsR37AI045898 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI ROTHENBERG, MARC E. · 2010 to 2019
$3.6M
Role of arginase in allergic airway inflammationR01AI053479 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI ROTHENBERG, MARC E. · 2003 to 2007
$1.8M
MECHANISMS OF EOSINOPHILIA IN EXPERIMENTAL ASTHMAR01AI042242 · NIAID · CHILDREN'S HOSPITAL MED CTR (CINCINNATI) · PI ROTHENBERG, MARC E. · 1998 to 2002
$729k
NIAID NIH HHS AI45898-04NIAID NIH HHS AI53479-01NIAID NIH HHS R01 AI045898NIAID NIH HHS R01 AI053479NIAID NIH HHS R01 AI42242-05NIAID NIH HHS R37 AI045898
6 · The paper itself

Abstract

Asthma is on the rise despite intense, ongoing research underscoring the need for new scientific inquiry. In an effort to provide unbiased insight into disease pathogenesis, we took an approach involving expression profiling of lung tissue from mice with experimental asthma. Employing asthma models induced by different allergens and protocols, we identified 6.5% of the tested genome whose expression was altered in an asthmatic lung. Notably, two phenotypically similar models of experimental asthma were shown to have distinct transcript profiles. Genes related to metabolism of basic amino acids, specifically the cationic amino acid transporter 2, arginase I, and arginase II, were particularly prominent among the asthma signature genes. In situ hybridization demonstrated marked staining of arginase I, predominantly in submucosal inflammatory lesions. Arginase activity was increased in allergen-challenged lungs, as demonstrated by increased enzyme activity, and increased levels of putrescine, a downstream product. Lung arginase activity and mRNA expression were strongly induced by IL-4 and IL-13, and were differentially dependent on signal transducer and activator of transcription 6. Analysis of patients with asthma supported the importance of this pathway in human disease. Based on the ability of arginase to regulate generation of NO, polyamines, and collagen, these results provide a basis for pharmacologically targeting arginine metabolism in allergic disorders.

Indexed as

AnimalsArginaseArginineAsthmaCytokinesDisease Models, AnimalGene Expression ProfilingGenetic MarkersHumansIsoenzymesLungMiceMice, Inbred BALB CMice, KnockoutNitric OxideOligonucleotide Array Sequence AnalysisArginaseArginineCytokinesGenetic MarkersIsoenzymesNitric OxideRNA, MessengerSTAT6 protein, humanStat6 protein, mouseSTAT6 Transcription FactorTrans-Activators

Identifiers

PMID12813022
PMCPMC161427
OpenAlexW2129431737

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.