Evidence map›Paper›PMID 25135336›Full record

ArticleNature communications2014

Molecular determinants of magnesium-dependent synaptic plasticity at electrical synapses formed by connexin36.

Nicolás Palacios-Prado, Sandrine Chapuis, Alejandro Panjkovich, Julien Fregeac, James I Nagy, Feliksas F Bukauskas

Open access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2014. 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
4.0field-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

29 citing papers in PubMed, 55 citations in OpenAlex.

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  10. GABAInternational journal of molecular sciences · 2021
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  12. Magnesium Is a Key Player in Neuronal Maturation and Neuropathology.International journal of molecular sciences · 2019
    Review
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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

6 authors at 3 institutions in 3 countries.

Nicolás Palacios-Prado1] Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461, USA [2] Grass Laboratory, Marine Biological Laboratory, Woods Hole, Woods Hole, Massachusetts 02543, USA.
Sandrine ChapuisDominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Alejandro PanjkovichEuropean Molecular Biology Laboratory, Hamburg Outstation, 22603 Hamburg, Germany.
Julien FregeacDominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
James I NagyDepartment of Physiology, University of Manitoba, Winnipeg, Manitoba, Canada R3E 0J9.
Feliksas F BukauskasDominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Albert Einstein College of Medicine · USEuropean Molecular Biology Laboratory · DEUniversity of Manitoba · CA

Funding

The Gateway Hypothesis: A new framework for unraveling diverse leukodystrophiesR01NS080153 · NINDS · COLORADO STATE UNIVERSITY · PI RASH, JOHN E · 2013 to 2017
$2.0M
Gating of Connexin-Based Gap Junction Channels and HemichannelsR01NS072238 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BUKAUSKAS, FELIKSAS · 2010 to 2013
$1.4M
NINDS NIH HHS R01 NS072238NINDS NIH HHS R01NS 072238NINDS NIH HHS R01 NS080153
6 · The paper itself

Abstract

Neuronal gap junction (GJ) channels composed of connexin36 (Cx36) play an important role in neuronal synchronization and network dynamics. Here we show that Cx36-containing electrical synapses between inhibitory neurons of the thalamic reticular nucleus are bidirectionally modulated by changes in intracellular free magnesium concentration ([Mg(2+)]i). Chimeragenesis demonstrates that the first extracellular loop of Cx36 contains a Mg(2+)-sensitive domain, and site-directed mutagenesis shows that the pore-lining residue D47 is critical in determining high Mg(2+)-sensitivity. Single-channel analysis of Mg(2+)-sensitive chimeras and mutants reveals that [Mg(2+)]i controls the strength of electrical coupling mostly via gating mechanisms. In addition, asymmetric transjunctional [Mg(2+)]i induces strong instantaneous rectification, providing a novel mechanism for electrical rectification in homotypic Cx36 GJs. We suggest that Mg(2+)-dependent synaptic plasticity of Cx36-containing electrical synapses could underlie neuronal circuit reconfiguration via changes in brain energy metabolism that affects neuronal levels of intracellular ATP and [Mg(2+)]i.

Indexed as

Adenosine TriphosphateAnimalsAntigensConnexin 43ConnexinsElectrical SynapsesEnergy MetabolismFemaleGap Junction delta-2 ProteinMagnesiumMaleMiceModels, AnimalNeuronal PlasticityNeuronsThalamic NucleiAdenosine TriphosphateAntigensConnexin 43ConnexinsD47 antigenGap Junction delta-2 ProteinMagnesium

Identifiers

PMID25135336
PMCPMC4142521
OpenAlexW1994344006

What OpenQuestion holds

Textmetadata
LicenceTDM
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.