Evidence map›Paper›PMID 30753170›Full record

ArticleJCI insight2019

Transcriptional analysis of Foxp3+ Tregs and functions of two identified molecules during resolution of ALI.

Jason R Mock, Catherine F Dial, Miriya K Tune, Dustin L Norton, Jessica R Martin, John C Gomez, Robert S Hagan, Hong Dang, Claire M Doerschuk

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

30 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. CNS1-dependent regulatory T cells shape recovery from acute lung injury.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
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  4. Regulation of inflammatory lung injury and repair by transforming growth factors.American journal of physiology. Lung cellular and molecular physiology · 2025
    Review
  5. Evaluating the role of alveolar macrophages in tolerance to ozone.Toxicological sciences : an official journal of the Society of Toxicology · 2025
    Article
  6. Review
  7. Review
  8. Stem cells, cell therapies, and bioengineering in lung biology and diseases 2023.American journal of physiology. Lung cellular and molecular physiology · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  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

9 authors at 2 institutions in 1 country.

Jason R MockDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine.
Catherine F DialDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine.
Miriya K TuneDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine.
Dustin L NortonDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine.
Jessica R MartinMarsico Lung Institute, and.
John C GomezMarsico Lung Institute, and.
Robert S HaganDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine.
Hong DangMarsico Lung Institute, and.
Claire M DoerschukDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine.
Lung Institute · USUniversity of North Carolina at Chapel Hill · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David Darr · 1985 to 2026
$201.5M
KOMP2-Phase3 Production and Phenotyping by the DTCC Consortium TCP Transfer to UC DavisUM1OD023221 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KC KENT LLOYD · 2016 to 2026
$45.7M
High-throughput targeted mutagenesis of mouse stem cell linesU01HG004080 · NHGRI · CHILDREN'S HOSPITAL & RES CTR AT OAKLAND · PI DE JONG, PIETER J. · 2006 to 2010
$28.1M
Production of Targeted Null Mutations for 10,000 Genes in C57BL/6 ES CellsU01HG004085 · NHGRI · REGENERON PHARMACEUTICALS, INC. · PI VALENZUELA, DAVID MANUEL · 2006 to 2010
$25.3M
Resource Section - Core 001U42OD010924 · OD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TERRY R MAGNUSON · 2012 to 2026
$24.5M
UCD KOMP PROJECT REPOSITORYU42RR024244 · NCRR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LLOYD, KC KENT · 2007 to 2010
$7.9M
Rho-mediated Signaling in Lung Endothelial Cells Induced by Neutrophil AdhesionR01HL114388 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BURRIDGE, KEITH, DOERSCHUK, CLAIRE M · 2012 to 2016
$3.0M
Trafficking and function of macrophage subpopulations within the lung microenvironment during pneumoniaR01HL145396 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DOERSCHUK, CLAIRE M · 2019 to 2022
$2.3M
Application of Omics in Lung DiseaseK12HL119998 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DOERSCHUK, CLAIRE M · 2013 to 2017
$1.4M
Regulatory T Cells Promote Alveolar Epithelial RepairK08HL129075 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MOCK, JASON ROBERT · 2016 to 2019
$685k
Defining the Role of Regulatory T Cell-Derived MMP12 in Acute Lung Injury ResolutionR03HL145255 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MOCK, JASON ROBERT · 2018 to 2019
$156k
NCI NIH HHS P30 CA016086NCRR NIH HHS U42 RR024244NHGRI NIH HHS U01 HG004080NHGRI NIH HHS U01 HG004085NHLBI NIH HHS K08 HL129075NHLBI NIH HHS K12 HL119998NHLBI NIH HHS R01 HL114388NHLBI NIH HHS R01 HL145396NHLBI NIH HHS R03 HL145255NIH HHS U42 OD010924NIH HHS UM1 OD023221
6 · The paper itself

Abstract

Recovery from acute lung injury (ALI) is an active process. Foxp3+ Tregs contribute to recovery from ALI through modulating immune responses and enhancing alveolar epithelial proliferation and tissue repair. The current study investigates Treg transcriptional profiles during resolution of ALI in mice. Tregs from either lung or splenic tissue were isolated from uninjured mice or mice recovering from ALI and then examined for differential gene expression between these conditions. In mice with ALI, Tregs isolated from the lungs had hundreds of differentially expressed transcripts compared with those from the spleen, indicating that organ specificity and microenvironment are critical in Treg function. These regulated transcripts suggest which intracellular signaling pathways modulate Treg behavior. Interestingly, several transcripts having no prior recognized function in Tregs were differentially expressed by lung Tregs during resolution. Further investigation into 2 identified transcripts, Mmp12 and Sik1, revealed that Treg-specific expression of each plays a role in Treg-promoted ALI resolution. This study provides potentially novel information describing the signals that may expand resident Tregs, recruit or retain them to the lung during ALI, and modulate their function. The results provide insight into both tissue- and immune microenvironment-specific transcriptional differences through which Tregs direct their effects.

Indexed as

TranscriptomeAcute Lung InjuryAnimalsChemokinesCytokinesDisease Models, AnimalFemaleForkhead Transcription FactorsGene ExpressionLungMaleMatrix Metalloproteinase 12MiceMice, Inbred C57BLMice, KnockoutNeutrophilsChemokinesCytokinesForkhead Transcription FactorsFoxp3 protein, mousematrix metallopeptidase 12, mouseMatrix Metalloproteinase 12Protein Serine-Threonine KinasesSik1 protein, mouseCellular immune responseImmunologyPulmonologyT cellsTranscription

Identifiers

PMID30753170
PMCPMC6482998
OpenAlexW2912580500

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.