Evidence map›Paper›PMID 23109423›Full record

ArticleMolecular and cellular biology2013

p38α mitogen-activated protein kinase depletion and repression of signal transduction to translation machinery by miR-124 and -128 in neurons.

Sarah K Lawson, Elena Y Dobrikova, Mayya Shveygert, Matthias Gromeier

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

29 citing papers in PubMed, 44 citations in OpenAlex.

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  8. Functions of p38 MAP Kinases in the Central Nervous System.Frontiers in molecular neuroscience · 2020
    Review
  9. Review
  10. Article
  11. Review
  12. An exploratory clinical study of p38Annals of clinical and translational neurology · 2018
    Article
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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

4 authors at 1 institution in 1 country.

Sarah K LawsonDivision of Neurosurgery, Department of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Elena Y Dobrikova
Mayya Shveygert
Matthias Gromeier
Duke Medical Center · US

Funding

ORGANIZATION AND FUNCTIONS OF CELLULAR STRUCTUREST32GM007184 · NIGMS · DUKE UNIVERSITY · PI JINKS-ROBERTSON, SUE · 1985 to 2019
$18.2M
Targeting Translation Control in Malignant GliomaR01CA124756 · NCI · DUKE UNIVERSITY · PI GROMEIER, MATTHIAS · 2007 to 2016
$2.6M
Oncolytic Virotherapy of Meningeal CancerR01CA140510 · NCI · DUKE UNIVERSITY · PI GROMEIER, MATTHIAS · 2009 to 2013
$1.6M
NCI NIH HHS CA140510NCI NIH HHS R01 CA124756NCI NIH HHS R01 CA140510NIGMS NIH HHS T32 GM007184
6 · The paper itself

Abstract

The p38α to p38δ mitogen-activated protein kinases (MAPKs) are central regulatory nodes coordinating acute stress and inflammatory responses. Their activation leads to rapid adjustment of protein synthesis, for instance translational induction of proinflammatory cytokines. The only known direct link of p38 to translation machinery is the MAPK signal-integrating kinase Mnk. Only p38α and p38β transcripts are ubiquitously expressed. These mRNAs encode highly conserved proteins that equally phosphorylate recombinant Mnk1 in vitro. We discovered that expression of the p38α protein, but not the p38β isoform, is suppressed in the brain. This is due to p38α depletion by two neuron-selective microRNAs (miRNAs), miR-124 and -128. Suppression of p38α protein was reversed by miR-124/-128 antisense oligonucleotides in primary explant neuronal cultures. Targeted p38α depletion reduced Mnk1 activation, which cannot be compensated by p38β. Our research shows that p38α alone controls acute stress and cytokine signaling from p38 MAPK to translation machinery. This regulatory axis is greatly diminished in neurons, which may insulate brain physiology and function from p38α-Mnk1-mediated signaling.

Indexed as

AnimalsBase SequenceCerebellumEukaryotic Initiation Factor-4EGene Expression Regulation, EnzymologicHEK293 CellsHumansMiceMice, Inbred BALB CMicroRNAsMitogen-Activated Protein Kinase 11Mitogen-Activated Protein Kinase 14Molecular Sequence DataNeuronsOligonucleotides, AntisenseOrgan Culture TechniquesEukaryotic Initiation Factor-4EMicroRNAsMIRN124 microRNA, humanMirn124 microRNA, mouseMIRN128 microRNA, humanMirn128 microRNA, mouseMitogen-Activated Protein Kinase 11Mitogen-Activated Protein Kinase 14Mknk1 protein, mouseOligonucleotides, AntisenseProtein Serine-Threonine Kinases

Identifiers

PMID23109423
PMCPMC3536301
OpenAlexW2142254799

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.