Evidence map›Paper›PMID 23325891›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

MiR-223 deficiency increases eosinophil progenitor proliferation.

Thomas X Lu, Eun-Jin Lim, John A Besse, Svetlana Itskovich, Andrew J Plassard, Patricia C Fulkerson, Bruce J Aronow, Marc E Rothenberg

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

55 citing papers in PubMed, 82 citations in OpenAlex.

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  11. Eosinophils: A Friend or Foe in Human Health and Diseases.Kidney diseases (Basel, Switzerland) · 2023
    Review
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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

8 authors at 2 institutions in 1 country.

Thomas X LuDivision of Allergy and Immunology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.
Eun-Jin Lim
John A Besse
Svetlana Itskovich
Andrew J Plassard
Patricia C Fulkerson
Bruce J Aronow
Marc E Rothenberg
University of Cincinnati · USCincinnati Children's Hospital Medical Center · US

Funding

Cincinnati Center for Clinical and Translational Sciences and TrainingUL1TR000077 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2012 to 2014
$9.9M
Medical Scientist Training ProgramT32GM063483 · NIGMS · UNIVERSITY OF CINCINNATI · PI KHURANA HERSHEY, GURJIT K. · 2002 to 2022
$6.7M
Regulation of Gastrointestinal EosinophilsR37AI045898 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI ROTHENBERG, MARC E. · 2010 to 2019
$3.6M
IL-13 Associated Eosinophil Lung ResponsesR01AI083450 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI ROTHENBERG, MARC E. · 2009 to 2013
$1.9M
Training Program in OrganogenesisT32HD046387 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI WYLIE, CHRISTOPHER C · 2006 to 2010
$1.1M
miR-21 in the Pathogenesis of AsthmaF30HL104892 · NHLBI · UNIVERSITY OF CINCINNATI · PI LU, THOMAS X · 2010 to 2012
$124k
NCATS NIH HHS UL1 TR000077NHLBI NIH HHS F30 HL104892NHLBI NIH HHS F30HL104892NIAID NIH HHS R01 AI083450NIAID NIH HHS R01AI083450NIAID NIH HHS R37 AI045898NICHD NIH HHS T32 HD046387NICHD NIH HHS T32HD046387NIGMS NIH HHS T32 GM063483NIGMS NIH HHS T32GM063483
6 · The paper itself

Abstract

Recently, microRNAs have been shown to be involved in hematopoietic cell development, but their role in eosinophilopoiesis has not yet been described. In this article, we show that miR-223 is upregulated during eosinophil differentiation in an ex vivo bone marrow-derived eosinophil culture system. Targeted ablation of miR-223 leads to an increased proliferation of eosinophil progenitors. We found upregulation of a miR-223 target gene, IGF1R, in the eosinophil progenitor cultures derived from miR-223(-/-) mice compared with miR-223(+/+) littermate controls. The increased proliferation of miR-223(-/-) eosinophil progenitors was reversed by treatment with an IGF1R inhibitor (picropodophyllin). Whole-genome microarray analysis of differentially regulated genes between miR-223(+/+) and miR-223(-/-) eosinophil progenitor cultures identified a specific enrichment in genes that regulate hematologic cell development. Indeed, miR-223(-/-) eosinophil progenitors had a delay in differentiation. Our results demonstrate that microRNAs regulate the development of eosinophils by influencing eosinophil progenitor growth and differentiation and identify a contributory role for miR-223 in this process.

Indexed as

Cell ProliferationMicroRNAsAnimalsBone Marrow CellsCell DifferentiationCells, CulturedDown-RegulationEosinophilsMiceMice, Inbred C57BLMice, KnockoutStem CellsUp-RegulationMicroRNAsMIRN223 microRNA, mouse

Identifiers

PMID23325891
PMCPMC3563857
OpenAlexW2166116651

What OpenQuestion holds

Textmetadata
LicenceTDM
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.