Evidence map›Paper›PMID 24077945›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2013

RGS3 controls T lymphocyte migration in a model of Th2-mediated airway inflammation.

Jesse W Williams, Douglas Yau, Nan Sethakorn, Jacob Kach, Eleanor B Reed, Tamson V Moore, Judy Cannon, Xiaohua Jin, Heming Xing, Anthony J Muslin and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Normal Thymocyte Egress, T Cell Trafficking, and CD4Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  8. Review
  9. Review
  10. Article
  11. Journal of psychiatry & neuroscience : JPN
    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

12 authors at 2 institutions in 1 country.

Jesse W WilliamsSection of Pulmonary and Critical Care, Dept. of Medicine, The Univ. of Chicago, 5841 S. Maryland Ave., MC6076, Rm. M-648, Chicago, IL 60637. ndulin@medicine.bsd.uchicago.edu.
Douglas Yau
Nan Sethakorn
Jacob Kach
Eleanor B Reed
Tamson V Moore
Judy Cannon
Xiaohua Jin
Heming Xing
Anthony J Muslin
Anne I Sperling
Nickolai O Dulin
University of Chicago · USWashington University in St. Louis · US

Funding

Ruth L. Kirschstein National Research Service Award (NRSA) Institutional Research Training Grant (Parent T32)T32HD007009 · NICHD · UNIVERSITY OF CHICAGO · PI NANCY B SCHWARTZ · 1985 to 2026
$13.0M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
Regulation and expression of HLA-G in asthmatic airwaysU19AI095230 · NIAID · UNIVERSITY OF CHICAGO · PI WHITE, STEVEN R · 2011 to 2016
$10.5M
CARDIOVASCULAR PATHOPHYSIOLOGY &BIOCHEMISTRY TRAININGT32HL007237 · NHLBI · UNIVERSITY OF CHICAGO · PI GETZ, GODFREY SHALOM · 1985 to 2011
$5.0M
Mechanisms of Resolution in Experimental AsthmaR01AI067697 · NIAID · UNIVERSITY OF CHICAGO · PI SPERLING, ANNE I. · 2007 to 2011
$1.9M
Novel functions of RGS3R01GM085058 · NIGMS · UNIVERSITY OF CHICAGO · PI DULIN, NICKOLAI O · 2009 to 2012
$1.2M
Dendritic cell produced IL-33 in Th2 responsesR21AI094408 · NIAID · UNIVERSITY OF CHICAGO · PI SPERLING, ANNE I. · 2011 to 2012
$418k
NHLBI NIH HHS T32-HL-007237NIAID NIH HHS R01-AI-067697NIAID NIH HHS R21-AI-094408NICHD NIH HHS T32-HD-009007NIGMS NIH HHS R01 GM-85058
6 · The paper itself

Abstract

T cell migration toward sites of antigen exposure is mediated by G protein signaling and is a key function in the development of immune responses. Regulators of G protein signaling (RGS) proteins modulate G protein signaling; however, their role in the regulation of adaptive immune responses has not been thoroughly explored. Herein we demonstrated abundant expression of the Gi/Gq-specific RGS3 in activated T cells, and that diminished RGS3 expression in a T cell thymoma increased cytokine-induced migration. To examine the role of endogenous RGS3 in vivo, mice deficient in the RGS domain (RGS3(ΔRGS)) were generated and tested in an experimental model of asthma. Compared with littermate controls, the inflammation in the RGS3(ΔRGS) mice was characterized by increased T cell numbers and the striking development of perivascular lymphoid structures. Surprisingly, while innate inflammatory cells were also increased in the lungs of RGS3(ΔRGS) mice, eosinophil numbers and Th2 cytokine production were equivalent to control mice. In contrast, T cell numbers in the draining lymph nodes (dLN) were reduced in the RGS3(ΔRGS), demonstrating a redistribution of T cells from the dLN to the lungs via increased RGS3(ΔRGS) T cell migration. Together these novel findings show a nonredundant role for endogenous RGS3 in controlling T cell migration in vitro and in an in vivo model of inflammation.

Indexed as

Cell MovementAnimalsApoptosisBlotting, WesternCell DifferentiationCell ProliferationDisease Models, AnimalFemaleFlow CytometryInflammationMaleMiceMice, Inbred C57BLMice, KnockoutPyroglyphidaeRespiratory MucosaRgs3 protein, mouseRGS ProteinsasthmaC cellG proteinsregulators of G protein signalingT cell

Identifiers

PMID24077945
PMCPMC3840273
OpenAlexW2157251537

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.