Evidence map›Paper›PMID 25633291›Full record

ArticleCell death & disease2015

miR-34a regulates cell proliferation, morphology and function of newborn neurons resulting in improved behavioural outcomes.

C Mollinari, M Racaniello, A Berry, M Pieri, M C de Stefano, A Cardinale, C Zona, F Cirulli, E Garaci, D Merlo

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

35 citing papers in PubMed, 58 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

C Mollinari1] Institute of Translational Pharmacology, National Research Council, Rome, Italy [2] Department of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
M RacanielloDepartment of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
A BerryDepartment of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
M Pieri1] Department of Experimental Medicine and Surgery, University of Rome 'Tor Vergata', Rome, Italy [2] Department of System Medicine, University of Rome 'Tor Vergata', Rome, Italy.
M C de StefanoDepartment of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
A CardinaleIRCCS San Raffaele Pisana, Rome, Italy.
C ZonaDepartment of System Medicine, University of Rome 'Tor Vergata', Rome, Italy.
F CirulliDepartment of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
E GaraciIRCCS San Raffaele Pisana, Rome, Italy.
D MerloDepartment of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
Istituto Superiore di Sanità · ITIRCCS Ospedale San Raffaele · ITUniversity of Rome Tor Vergata · ITNational Research Council · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

miR-34a is involved in the regulation of the fate of different cell types. However, the mechanism by which it controls the differentiation programme of neural cells remains largely unknown. Here, we investigated the role of miR-34a in neurogenesis and maturation of developing neurons and identified Doublecortin as a new miR-34a target. We found that the overexpression of miR-34a in vitro significantly increases precursor proliferation and influences morphology and function of developing neurons. Indeed, miR-34a overexpressing neurons showed a decreased expression of several synaptic proteins and receptor subunits, a decrement of NMDA-evoked current density and, interestingly, a more efficient response to synaptic stimulus. In vivo, miR-34a overexpression showed stage-specific effects. In neural progenitors, miR-34a overexpression promoted cell proliferation, in migratory neuroblasts reduced the migration and in differentiating newborn neurons modulated process outgrowth and complexity. Importantly, we found that rats overexpressing miR-34a in the brain have better learning abilities and reduced emotionality.

Indexed as

Behavior, AnimalCell ShapeNeurogenesisAnimalsBase SequenceBromodeoxyuridineCell DifferentiationCell MovementCell ProliferationCells, CulturedCerebral CortexCognitionDependovirusDoublecortin Domain ProteinsDoublecortin ProteinEmotionsBromodeoxyuridineDcx protein, ratDoublecortin Domain ProteinsDoublecortin ProteinMicroRNAsMicrotubule-Associated ProteinsMIRN34 microRNA, ratNeuropeptides

Identifiers

PMID25633291
PMCPMC4669781
OpenAlexW2001836517

What OpenQuestion holds

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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.