Evidence map›Paper›PMID 23251709›Full record

ArticlePloS one2012

miR-22 controls Irf8 mRNA abundance and murine dendritic cell development.

Haiyan S Li, Nathaniel Greeley, Naoshi Sugimoto, Yong-Jun Liu, Stephanie S Watowich

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. The Role of microRNAs in Inflammation.International journal of molecular sciences · 2022
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Regulating IRFs in IFN Driven Disease.Frontiers in immunology · 2019
    Review
  9. Article
  10. Two microRNA signatures for malignancy and immune infiltration predict overall survival in advanced epithelial ovarian cancer.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2017
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. miR-22 in cardiac remodeling and disease.Trends in cardiovascular medicine · 2014
    Review
  18. The role of microRNAs in lymphopoiesis.International journal of hematology · 2014
    Review
  19. Article
  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

5 authors at 2 institutions in 1 country.

Haiyan S LiDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA. haiyanli@mdanderson.org
Nathaniel Greeley
Naoshi Sugimoto
Yong-Jun Liu
Stephanie S Watowich
The University of Texas MD Anderson Cancer Center · USBaylor University · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Pathways regulating plasmacytoid dendritic cells in Peyers PatchesR21AI098099 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WATOWICH, STEPHANIE S · 2012 to 2013
$435k
Cytokine Regulation of Dendritic Cell DevelopmentR21AI073587 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WATOWICH, STEPHANIE S · 2007 to 2008
$409k
NCI NIH HHS P30 CA016672NIAID NIH HHS AI073587NIAID NIH HHS AI098099NIAID NIH HHS R21 AI073587NIAID NIH HHS R21 AI098099
6 · The paper itself

Abstract

MicroRNAs (miRNAs) have emerged as critical regulators of many cellular responses, through the action of miRNA-induced silencing complex (miRISC)- or miRNA ribonucleoprotein complex (miRNP)-mediated gene repression. Here we studied the role of miRNAs in the development of dendritic cells (DCs), an important immune cell type that is divided into conventional DC (cDC) and plasmacytoid DC (pDC) subsets. We found that miR-22 was highly expressed in mouse CD11c(+) CD11b(+) B220(-) cDCs compared to pDCs, and was induced in DC progenitor cell cultures with GM-CSF, which stimulate CD11c(+) CD11b(+) B220(-) cDC differentiation. Enforced overexpression of miR-22 during DC development enhanced CD11c(+) CD11b(+) B220(-) cDC generation at the expense of pDCs, while miR-22 knockdown demonstrated opposite effects. Moreover, overexpression and knockdown of miR-22 showed significant effects on the mRNA abundance of Irf8, which encodes the transcription factor IRF8 that plays essential roles in DC development. Luciferase reporter assays confirmed that miR-22 binds directly to the 3'UTR of the mouse Irf8 mRNA. Collectively, these results suggest that miR-22 targets Irf8 mRNA for posttranscriptional repression and controls DC subset differentiation.

Indexed as

3' Untranslated RegionsAnimalsCD11b AntigenCD11c AntigenCell DifferentiationDendritic CellsGranulocyte-Macrophage Colony-Stimulating FactorInterferon Regulatory Factor-8Interferon Regulatory FactorsLeukocyte Common AntigensMiceMice, Inbred C57BLMicroRNAsRNA, Messenger3' Untranslated RegionsCD11b AntigenCD11c AntigenGranulocyte-Macrophage Colony-Stimulating FactorInterferon Regulatory Factor-8Interferon Regulatory FactorsLeukocyte Common AntigensMicroRNAsMirn22 microRNA, mouseRNA, Messenger

Identifiers

PMID23251709
PMCPMC3522651
OpenAlexW2050769787

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.