Evidence map›Paper›PMID 25761522›Full record

ArticleMolecular brain2015

The novel protein kinase C epsilon isoform at the adult neuromuscular synapse: location, regulation by synaptic activity-dependent muscle contraction through TrkB signaling and coupling to ACh release.

Teresa Obis, Núria Besalduch, Erica Hurtado, Laura Nadal, Manel M Santafe, Neus Garcia, Marta Tomàs, Mercedes Priego, Maria A Lanuza, Josep Tomàs

Open access · goldAbstract read
In one paragraph

Article in Molecular brain, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-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

23 citing papers in PubMed, 37 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 1 institution in 1 country.

Teresa ObisUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. teresa.obis@gmail.com.
Núria BesalduchUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. nbesal@yahoo.es.
Erica HurtadoUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. erica.hurtado@urv.cat.
Laura NadalUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. lauranadalm@gmail.com.
Manel M SantafeUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. manuel.santafe@urv.cat.
Neus GarciaUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. ngs@fmcs.urv.es.
Marta TomàsUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. marta.tomas@urv.cat.
Mercedes PriegoUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. merce18pl@hotmail.com.
Maria A LanuzaUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. mariaangel.lanuza@urv.cat.
Josep TomàsUnitat d'Histologia i Neurobiologia (UHN). Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Sant Llorenç 21, 43201, Reus, Spain. josepmaria.tomas@urv.cat.
Universidad Rovira i Virgili · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProtein kinase C (PKC) regulates a variety of neural functions, including neurotransmitter release. Although various PKC isoforms can be expressed at the synaptic sites and specific cell distribution may contribute to their functional diversity, little is known about the isoform-specific functions of PKCs in neuromuscular synapse. The present study is designed to examine the location of the novel isoform nPKCε at the neuromuscular junction (NMJ), their synaptic activity-related expression changes, its regulation by muscle contraction, and their possible involvement in acetylcholine release.

resultsWe use immunohistochemistry and confocal microscopy to demonstrate that the novel isoform nPKCε is exclusively located in the motor nerve terminals of the adult rat NMJ. We also report that electrical stimulation of synaptic inputs to the skeletal muscle significantly increased the amount of nPKCε isoform as well as its phosphorylated form in the synaptic membrane, and muscle contraction is necessary for these nPKCε expression changes. The results also demonstrate that synaptic activity-induced muscle contraction promotes changes in presynaptic nPKCε through the brain-derived neurotrophic factor (BDNF)-mediated tyrosine kinase receptor B (TrkB) signaling. Moreover, nPKCε activity results in phosphorylation of the substrate MARCKS involved in actin cytoskeleton remodeling and related with neurotransmission. Finally, blocking nPKCε with a nPKCε-specific translocation inhibitor peptide (εV1-2) strongly reduces phorbol ester-induced ACh release potentiation, which further indicates that nPKCε is involved in neurotransmission.

conclusionsTogether, these results provide a mechanistic insight into how synaptic activity-induced muscle contraction could regulate the presynaptic action of the nPKCε isoform and suggest that muscle contraction is an important regulatory step in TrkB signaling at the NMJ.

Indexed as

Muscle ContractionAcetylcholineAgingAnimalsAnimals, NewbornElectrophysiological PhenomenaIntracellular Signaling Peptides and ProteinsIsoenzymesMaleMembrane ProteinsModels, BiologicalMuscle, SkeletalMyristoylated Alanine-Rich C Kinase SubstrateNeuromuscular JunctionPhosphorylationProtein Kinase C-epsilonAcetylcholineIntracellular Signaling Peptides and ProteinsIsoenzymesMarcks protein, ratMembrane ProteinsMyristoylated Alanine-Rich C Kinase SubstrateProtein Kinase C-epsilonReceptor, trkBTetradecanoylphorbol Acetate

Identifiers

PMID25761522
PMCPMC4348107
OpenAlexW2106601195

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Registered trials

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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.