Evidence map›Paper›PMID 32209973›Full record

ArticleInternational journal of molecular sciences2020

Myocyte Enhancer Factor 2A (MEF2A) Defines Oxytocin-Induced Morphological Effects and Regulates Mitochondrial Function in Neurons.

Magdalena Meyer, Kerstin Kuffner, Julia Winter, Inga D Neumann, Christian H Wetzel, Benjamin Jurek

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.5field-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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
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

6 authors at 1 institution in 1 country.

Magdalena MeyerDepartment of Behavioral and Molecular Neurobiology, University of Regensburg, 93040 Regensburg, Germany.ORCID 0000-0002-5388-3850
Kerstin KuffnerDepartment of Psychiatry and Psychotherapy, University of Regensburg, 93040 Regensburg, Germany.
Julia WinterDepartment of Behavioral and Molecular Neurobiology, University of Regensburg, 93040 Regensburg, Germany.
Inga D NeumannDepartment of Behavioral and Molecular Neurobiology, University of Regensburg, 93040 Regensburg, Germany.
Christian H WetzelDepartment of Psychiatry and Psychotherapy, University of Regensburg, 93040 Regensburg, Germany.ORCID 0000-0002-5762-0003
Benjamin JurekDepartment of Behavioral and Molecular Neurobiology, University of Regensburg, 93040 Regensburg, Germany.ORCID 0000-0001-7124-510X
University of Regensburg · DE

Funding

Deutsche Forschungsgemeinschaft 422182557Deutsche Forschungsgemeinschaft GRK2174Deutsche Forschungsgemeinschaft JU3039/1-1Deutsche Forschungsgemeinschaft Ne465/27-1Deutsche Forschungsgemeinschaft Ne465/31-1Deutsche Forschungsgemeinschaft WE2289/10-1
6 · The paper itself

Abstract

The neuropeptide oxytocin (OT) is a well-described modulator of socio-emotional traits, such as anxiety, stress, social behavior, and pair bonding. However, when dysregulated, it is associated with adverse psychiatric traits, such as various aspects of autism spectrum disorder (ASD). In this study, we identify the transcription factor myocyte enhancer factor 2A (MEF2A) as the common link between OT and cellular changes symptomatic for ASD, encompassing neuronal morphology, connectivity, and mitochondrial function. We provide evidence for MEF2A as the decisive factor defining the cellular response to OT: while OT induces neurite retraction in MEF2A expressing neurons, OT causes neurite outgrowth in absence of MEF2A. A CRISPR-Cas-mediated knockout of MEF2A and retransfection of an active version or permanently inactive mutant, respectively, validated our findings. We also identified the phosphatase calcineurin as the main upstream regulator of OT-induced MEF2A signaling. Further, MEF2A signaling dampens mitochondrial functioning in neurons, as MEF2A knockout cells show increased maximal cellular respiration, spare respiratory capacity, and total cellular ATP. In summary, we reveal a central role for OT-induced MEF2A activity as major regulator of cellular morphology as well as neuronal connectivity and mitochondrial functioning, with broad implications for a potential treatment of disorders based on morphological alterations or mitochondrial dysfunction.

Indexed as

AnimalsCell LineCell RespirationGene Expression RegulationGene Knockdown TechniquesMEF2 Transcription FactorsMitochondriaNeuronsOxytocinRatsMEF2A protein, ratMEF2 Transcription FactorsOxytocinautismCRISPR-CashyperconnectivityMEF2Amorphologyneurite outgrowthneurite retractionoxytocin

Identifiers

PMID32209973
PMCPMC7139413
OpenAlexW3007760832

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.