Evidence map›Paper›PMID 25210157›Full record

ArticleJournal of neurophysiology2015

New insights into short-term synaptic facilitation at the frog neuromuscular junction.

Jun Ma, Lauren Kelly, Justin Ingram, Thomas J Price, Stephen D Meriney, Markus Dittrich

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

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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.

Jun MaBiomedical Applications Group, Pittsburgh Supercomputing Center, Carnegie Mellon University, Pittsburgh, Pennsylvania; Joint Carnegie Mellon-University of Pittsburgh PhD Program in Computational Biology, School of Computer Science, Carnegie Mellon University, Pittsburgh, Pennsylvania;
Lauren KellyDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania; and.
Justin IngramDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania; and.
Thomas J PriceDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania; and.
Stephen D MerineyDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania; and.
Markus DittrichBiomedical Applications Group, Pittsburgh Supercomputing Center, Carnegie Mellon University, Pittsburgh, Pennsylvania; Department of Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania; and Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania dittrich@psc.edu.

Funding

TrainingP41GM103712 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FAEDER, JAMES · 2012 to 2021
$16.3M
CRCNS: Transmitter Release Site Organization in Plasticity and Disease at the NMJR01NS090644 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BLANPIED, THOMAS A, LAGHAEI, ROZITA · 2014 to 2018
$1.9M
NIGMS NIH HHS P41 GM-103712NIGMS NIH HHS P41 GM103712NINDS NIH HHS R01 NS-090644NINDS NIH HHS R01 NS090644
6 · The paper itself

Abstract

Short-term synaptic facilitation occurs during high-frequency stimulation, is known to be dependent on presynaptic calcium ions, and persists for tens of milliseconds after a presynaptic action potential. We have used the frog neuromuscular junction as a model synapse for both experimental and computer simulation studies aimed at testing various mechanistic hypotheses proposed to underlie short-term synaptic facilitation. Building off our recently reported excess-calcium-binding-site model of synaptic vesicle release at the frog neuromuscular junction (Dittrich M, Pattillo JM, King JD, Cho S, Stiles JR, Meriney SD. Biophys J 104: 2751-2763, 2013), we have investigated several mechanisms of short-term facilitation at the frog neuromuscular junction. Our studies place constraints on previously proposed facilitation mechanisms and conclude that the presence of a second class of calcium sensor proteins distinct from synaptotagmin can explain known properties of facilitation observed at the frog neuromuscular junction. We were further able to identify a novel facilitation mechanism, which relied on the persistent binding of calcium-bound synaptotagmin molecules to lipids of the presynaptic membrane. In a real physiological context, both mechanisms identified in our study (and perhaps others) may act simultaneously to cause the experimentally observed facilitation. In summary, using a combination of computer simulations and physiological recordings, we have developed a stochastic computer model of synaptic transmission at the frog neuromuscular junction, which sheds light on the facilitation mechanisms in this model synapse.

Indexed as

AnimalsCalciumCalcium-Binding ProteinsCalcium Channels, N-TypeComputer SimulationKineticsMembrane LipidsMicroelectrodesModels, NeurologicalNeuromuscular JunctionNeuronal PlasticityPresynaptic TerminalsRana pipiensStochastic ProcessesSynaptic TransmissionSynaptic VesiclesCalciumCalcium-Binding ProteinsCalcium Channels, N-TypeMembrane Lipidsfrog neuromuscular junctionMCellshort-term synaptic plasticitystochastic simulationsynaptic vesicle release

Identifiers

PMID25210157
PMCPMC4294575

What OpenQuestion holds

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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.