Evidence map›Paper›PMID 29103941›Full record

ArticleCurrent biology : CB2017

Asymmetry of an Intracellular Scaffold at Vertebrate Electrical Synapses.

Audrey J Marsh, Jennifer Carlisle Michel, Anisha P Adke, Emily L Heckman, Adam C Miller

Abstract read
In one paragraph

Article in Current biology : CB, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Defining the electrical synapse.Nature reviews. Neuroscience · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Electrical Synapses Mediate Embryonic Hyperactivity in a Zebrafish Model of Fragile X Syndrome.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Gap junction Delta-2b (Frontiers in cell and developmental biology · 2023
    Article
  10. ThemicroPublication biology · 2022
    Article
  11. On the Diverse Functions of Electrical Synapses.Frontiers in cellular neuroscience · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Network Architecture of Gap Junctional Coupling among Parallel Processing Channels in the Mammalian Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Audrey J MarshUniversity of Oregon, Institute of Neuroscience, Department of Biology, 1254 University of Oregon, Eugene, OR 97403, USA.
Jennifer Carlisle MichelUniversity of Oregon, Institute of Neuroscience, Department of Biology, 1254 University of Oregon, Eugene, OR 97403, USA.
Anisha P AdkeUniversity of Oregon, Institute of Neuroscience, Department of Biology, 1254 University of Oregon, Eugene, OR 97403, USA.
Emily L HeckmanUniversity of Oregon, Institute of Neuroscience, Department of Biology, 1254 University of Oregon, Eugene, OR 97403, USA.
Adam C MillerUniversity of Oregon, Institute of Neuroscience, Department of Biology, 1254 University of Oregon, Eugene, OR 97403, USA. Electronic address: acmiller@uoregon.edu.

Funding

Molecular Mechanisms of Electrical Synapse Formation in VivoR01NS105758 · NINDS · UNIVERSITY OF OREGON · PI Adam C Miller · 2019 to 2026
$3.7M
Molecular mechanisms of electrical synapse formation in vivoR00NS085035 · NINDS · UNIVERSITY OF OREGON · PI MILLER, ADAM C · 2016 to 2018
$747k
NINDS NIH HHS R00 NS085035NINDS NIH HHS R01 NS105758
6 · The paper itself

Abstract

Neuronal synaptic connections are either chemical or electrical, and these two types of synapses work together to dynamically define neural circuit function [1]. Although we know a great deal about the molecules that support chemical synapse formation and function, we know little about the macromolecular complexes that regulate electrical synapses. Electrical synapses are created by gap junction (GJ) channels that provide direct ionic communication between neurons [2]. Although they are often molecularly and functionally symmetric, recent work has found that pre- and postsynaptic neurons can contribute different GJ-forming proteins, creating molecularly asymmetric channels that are correlated with functional asymmetry at the synapse [3, 4]. Associated with the GJs are structures observed by electron microscopy termed the electrical synapse density (ESD) [5]. The ESD has been suggested to be critical for the formation and function of the electrical synapse, yet the biochemical makeup of these structures is poorly understood. Here we find that electrical synapse formation in vivo requires an intracellular scaffold called Tight Junction Protein 1b (Tjp1b). Tjp1b is localized to the electrical synapse, where it is required for the stabilization of the GJs and for electrical synapse function. Strikingly, we find that Tjp1b protein localizes and functions asymmetrically, exclusively on the postsynaptic side of the synapse. Our findings support a novel model of electrical synapse molecular asymmetry at the level of an intracellular scaffold that is required for building the electrical synapse. We propose that such ESD asymmetries could be used by all nervous systems to support molecular and functional asymmetries at electrical synapses.

Indexed as

AnimalsConnexinsElectrical SynapsesGap JunctionsIon ChannelsNervous SystemNeuronsSynapsesTight JunctionsVertebratesZebrafishZebrafish ProteinsZonula Occludens-1 ProteinConnexinsIon ChannelsZebrafish ProteinsZonula Occludens-1 Proteinconnexinelectrical synapsegap junctionMAGUK scaffoldneural circuit wiring

Identifiers

PMID29103941
PMCPMC5698123

What OpenQuestion holds

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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.