Evidence map›Paper›PMID 24463820›Full record

ArticleJournal of cell science2014

AII amacrine cells discriminate between heterocellular and homocellular locations when assembling connexin36-containing gap junctions.

Arndt Meyer, Gerrit Hilgen, Birthe Dorgau, Esther M Sammler, Reto Weiler, Hannah Monyer, Karin Dedek, Sheriar G Hormuzdi

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Trafficking of Connexin36 (Cx36) in the early secretory pathway.bioRxiv : the preprint server for biology · 2024
    Article
  5. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. An Update on Connexin Gap Junction and Hemichannels in Diabetic Retinopathy.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Localization of Retinal CaFrontiers in molecular neuroscience · 2019
    Article
  17. Article
  18. Differential Distribution of Retinal CaFrontiers in molecular neuroscience · 2017
    Article
  19. Article
  20. Article
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

8 authors at 3 institutions in 2 countries.

Arndt MeyerResearch Centre for Neurosensory Sciences/Department of Neurobiology, University of Oldenburg, 26111 Oldenburg, Germany.
Gerrit Hilgen
Birthe Dorgau
Esther M Sammler
Reto Weiler
Hannah Monyer
Karin Dedek
Sheriar G Hormuzdi
Carl von Ossietzky Universität Oldenburg · DEUniversity of Dundee · GBGerman Cancer Research Center · DE

Funding

Wellcome TrustWellcome Trust WT078791
6 · The paper itself

Abstract

Electrical synapses (gap junctions) rapidly transmit signals between neurons and are composed of connexins. In neurons, connexin36 (Cx36) is the most abundant isoform; however, the mechanisms underlying formation of Cx36-containing electrical synapses are unknown. We focus on homocellular and heterocellular gap junctions formed by an AII amacrine cell, a key interneuron found in all mammalian retinas. In mice lacking native Cx36 but expressing a variant tagged with enhanced green fluorescent protein at the C-terminus (KO-Cx36-EGFP), heterocellular gap junctions formed between AII cells and ON cone bipolar cells are fully functional, whereas homocellular gap junctions between two AII cells are not formed. A tracer injected into an AII amacrine cell spreads into ON cone bipolar cells but is excluded from other AII cells. Reconstruction of Cx36-EGFP clusters on an AII cell in the KO-Cx36-EGFP genotype confirmed that the number, but not average size, of the clusters is reduced - as expected for AII cells lacking a subset of electrical synapses. Our studies indicate that some neurons exhibit at least two discriminatory mechanisms for assembling Cx36. We suggest that employing different gap-junction-forming mechanisms could provide the means for a cell to regulate its gap junctions in a target-cell-specific manner, even if these junctions contain the same connexin.

Indexed as

Protein MultimerizationAmacrine CellsAnimalsConnexinsGap Junction delta-2 ProteinGap JunctionsGene Knockout TechniquesGreen Fluorescent ProteinsMice, KnockoutProtein TransportRecombinant Fusion ProteinsRetinaRetinal Cone Photoreceptor CellsZonula Occludens-1 Proteinconnexin 45Connexinsenhanced green fluorescent proteinGap Junction delta-2 ProteinGreen Fluorescent ProteinsRecombinant Fusion ProteinsTjp1 protein, mouseZonula Occludens-1 ProteinAmacrine cellBipolar cellconnexinElectrical synapseGap junctionRetina

Identifiers

PMID24463820
PMCPMC3953814
OpenAlexW2109384917

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.