Evidence map›Paper›PMID 18369473›Full record

ArticlePLoS pathogens2008

Cationic amino acid transporter-2 regulates immunity by modulating arginase activity.

Robert W Thompson, John T Pesce, Thirumalai Ramalingam, Mark S Wilson, Sandy White, Allen W Cheever, Stacy M Ricklefs, Stephen F Porcella, Lili Li, Lesley G Ellies and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.4field-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

49 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
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  7. Review
  8. Zoledronate alters natural progression of tissue-engineered vascular grafts.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  9. Metabolomic Reprogramming of C57BL/6-Macrophages during Early Infection withInternational journal of molecular sciences · 2021
    Article
  10. Cardiac regenerative capacity: an evolutionary afterthought?Cellular and molecular life sciences : CMLS · 2021
    Review
  11. Article
  12. Article
  13. Review
  14. Thermal injury initiates pervasive fibrogenesis in skeletal muscle.American journal of physiology. Cell physiology · 2020
    Article
  15. Review
  16. Article
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  19. Article
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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

11 authors at 4 institutions in 1 country.

Robert W ThompsonImmunopathogenesis Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
John T Pesce
Thirumalai Ramalingam
Mark S Wilson
Sandy White
Allen W Cheever
Stacy M Ricklefs
Stephen F Porcella
Lili Li
Lesley G Ellies
Thomas A Wynn
National Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USBiomedical Research Institute · USUniversity of California, San Diego · US

Funding

Infectious Diseases Research Technologies Core - RMLZICAI001052 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CHERRY, JAMES · 2009 to 2025
$133.3M
Immunological Intervention In SchistosomiasisZ01AI000829 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI WYNN, THOMAS · 1998 to 2008
$3.4M
Role of the chronic inflammatory mediator NO in early mammary tumorigenesisK22CA118182 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLIES, LESLEY G · 2006 to 2008
$442k
Intramural NIH HHSNCI NIH HHS CA118182NCI NIH HHS K22 CA118182
6 · The paper itself

Abstract

Cationic amino acid transporters (CAT) are important regulators of NOS2 and ARG1 activity because they regulate L-arginine availability. However, their role in the development of Th1/Th2 effector functions following infection has not been investigated. Here we dissect the function of CAT2 by studying two infectious disease models characterized by the development of polarized Th1 or Th2-type responses. We show that CAT2(-/-) mice are significantly more susceptible to the Th1-inducing pathogen Toxoplasma gondii. Although T. gondii infected CAT2(-/-) mice developed stronger IFN-gamma responses, nitric oxide (NO) production was significantly impaired, which contributed to their enhanced susceptibility. In contrast, CAT2(-/-) mice infected with the Th2-inducing pathogen Schistosoma mansoni displayed no change in susceptibility to infection, although they succumbed to schistosomiasis at an accelerated rate. Granuloma formation and fibrosis, pathological features regulated by Th2 cytokines, were also exacerbated even though their Th2 response was reduced. Finally, while IL-13 blockade was highly efficacious in wild-type mice, the development of fibrosis in CAT2(-/-) mice was largely IL-13-independent. Instead, the exacerbated pathology was associated with increased arginase activity in fibroblasts and alternatively activated macrophages, both in vitro and in vivo. Thus, by controlling NOS2 and arginase activity, CAT2 functions as a potent regulator of immunity.

Indexed as

AnimalsArginaseCationic Amino Acid Transporter 2Cell ProliferationCells, CulturedDisease Models, AnimalFemaleFibroblastsFibrosisGene ExpressionGene SilencingGranulomaImmunityLiverLungLung Diseases, ParasiticArginaseCationic Amino Acid Transporter 2Nitric Oxide

Identifiers

PMID18369473
PMCPMC2265428
OpenAlexW1995634355

What OpenQuestion holds

Textmetadata
LicenceCC0
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.