Evidence map›Paper›PMID 22919664›Full record

ArticleFrontiers in cellular and infection microbiology2012

MiR-155 induction by microbes/microbial ligands requires NF-κB-dependent de novo protein synthesis.

Thomas J Cremer, Kavin Fatehchand, Prexy Shah, Devyn Gillette, Hemal Patel, Rachel L Marsh, Beth Y Besecker, Murugesan V S Rajaram, Estelle Cormet-Boyaka, Thirumala-Devi Kanneganti and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Innate Immune Recognition: An Issue More Complex Than Expected.Frontiers in cellular and infection microbiology · 2019
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Modulation of Host miRNAs by Intracellular Bacterial Pathogens.Frontiers in cellular and infection microbiology · 2016
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

13 authors at 1 institution in 1 country.

Thomas J CremerMolecular, Cellular, and Developmental Biology Program, The Ohio State University Columbus, OH, USA.
Kavin Fatehchand
Prexy Shah
Devyn Gillette
Hemal Patel
Rachel L Marsh
Beth Y Besecker
Murugesan V S Rajaram
Estelle Cormet-Boyaka
Thirumala-Devi Kanneganti
Larry S Schlesinger
Jonathan P Butchar
Susheela Tridandapani
The Ohio State University · US

Funding

Vaccines and Therapies Against BotulismU54AI057153 · NIAID · UNIVERSITY OF CHICAGO · PI SCHLESINGER, LARRY S. · 2003 to 2013
$87.6M
Translational Training Grant in Experimental TherapeuticsK12CA133250 · NCI · OHIO STATE UNIVERSITY · PI WILLIAM E. CARSON, Rosa Lapalombella · 2008 to 2026
$15.0M
Interdisciplinary Study of the Microbe-Host InterfaceT32AI065411 · NIAID · OHIO STATE UNIVERSITY · PI SCHLESINGER, LARRY S. · 2007 to 2011
$592k
NCI NIH HHS K12 CA133250NCI NIH HHS L12 CA133250.NIAID NIH HHS 1-T32-AI-065411NIAID NIH HHS 1-U54-AI-057153NIAID NIH HHS T32 AI065411NIAID NIH HHS U54 AI057153
6 · The paper itself

Abstract

MiR-155 regulates numerous aspects of innate and adaptive immune function. This miR is induced in response to Toll-like receptor ligands, cytokines, and microbial infection. We have previously shown that miR-155 is induced in monocytes/macrophages infected with Francisella tularensis and suppresses expression of the inositol phosphatase SHIP to enhance activation of the PI3K/Akt pathway, which in turn promotes favorable responses for the host. Here we examined how miR-155 expression is regulated during infection. First, our data demonstrate that miR-155 can be induced through soluble factors of bacterial origin and not the host. Second, miR-155 induction is not a direct effect of infection and it requires NF-κB signaling to up-regulate fos/jun transcription factors. Finally, we demonstrate that the requirement for NF-κB-dependent de novo protein synthesis is globally shared by microbial ligands and live bacteria. This study provides new insight into the complex regulation of miR-155 during microbial infection.

Indexed as

Cells, CulturedFrancisella tularensisHumansMicroRNAsMonocytesNF-kappa BProtein BiosynthesisMicroRNAsMIRN155 microRNA, humanNF-kappa Bmicrobial pathogenesismicroRNAmiR-155

Identifiers

PMID22919664
PMCPMC3417573
OpenAlexW1966688093

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.