Evidence map›Paper›PMID 31172263›Full record

ArticleBrain structure & function2019

Connexin-36 distribution and layer-specific topography in the cat retina.

Ildikó Telkes, Péter Kóbor, József Orbán, Tamás Kovács-Öller, Béla Völgyi, Péter Buzás

Open access · hybridAbstract read
In one paragraph

Article in Brain structure & function, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. An Update on Connexin Gap Junction and Hemichannels in Diabetic Retinopathy.International journal of molecular sciences · 2021
    Review
  5. Expression of CaInternational journal of molecular sciences · 2019
    Review
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 1 institution in 1 country.

Ildikó TelkesInstitute of Physiology, Medical School, University of Pécs, Szigeti út 12, Pécs, 7624, Hungary.
Péter KóborInstitute of Physiology, Medical School, University of Pécs, Szigeti út 12, Pécs, 7624, Hungary.
József OrbánSzentágothai Research Centre, University of Pécs, Pécs, 7624, Hungary.
Tamás Kovács-ÖllerSzentágothai Research Centre, University of Pécs, Pécs, 7624, Hungary.
Béla VölgyiSzentágothai Research Centre, University of Pécs, Pécs, 7624, Hungary.
Péter BuzásInstitute of Physiology, Medical School, University of Pécs, Szigeti út 12, Pécs, 7624, Hungary. peter.buzas@aok.pte.hu.ORCID http://orcid.org/0000-0002-4390-3360
University of Pecs · HU

Funding

Általános Orvostudományi Kar, Pécsi Tudományegyetem ÁOK-KA 2013/6Emberi Eroforrások Minisztériuma TÁMOP-4.2.4.A/ 2-11/1-2012-0001Emberi Eroforrások Minisztériuma UNKP-17-3-I-PTE-155Nemzeti Kutatási, Fejlesztési és Innovációs Hivatal 2017-1.2.1.-NKP-2017Nemzeti Kutatási, Fejlesztési és Innovációs Hivatal 20765-3/2018/FEKUTSTRATOrszágos Tudományos Kutatási Alapprogramok K108747Országos Tudományos Kutatási Alapprogramok NN128293
6 · The paper itself

Abstract

Connexin-36 (Cx36) is the major constituent of mammalian retinal gap junctions positioned in key signal pathways. Here, we examined the laminar and large-scale topographical distribution of Cx36 punctate immunolabels in the retina of the cat, a classical model of the mammalian visual system. Calretinin-immunoreactive (CaR-IR) cell populations served to outline the nuclear and plexiform layers and to stain specific neuronal populations. CaR-IR cells included horizontal cells in the outer retina, numerous amacrine cells, and scattered cells in the ganglion cell layer. Cx36-IR plaques were found among horizontal cell dendrites albeit without systematic colocalization of the two labels. Diffuse Cx36 immunoreactivity was found in the cytoplasm of AII amacrine cells, but no colocalization of Cx36 plaques was observed with either the perikarya or the long varicose dendrites of the CaR-IR non-AII amacrine cells. Cx36 puncta were seen throughout the entire inner plexiform layer showing their highest density in the ON sublamina. The densities of AII amacrine cell bodies and Cx36 plaques in the ON sublamina were strongly correlated across a wide range of eccentricities suggesting their anatomical association. However, the high number of plaques per AII cell suggests that a considerable fraction of Cx36 gap junctions in the ON sublamina is formed by other cell types than AII amacrine cells drawing attention to extensive but less studied electrically coupled networks.

Indexed as

Amacrine CellsAnimalsCalbindin 2CatsConnexinsDendritesGap Junction delta-2 ProteinGap JunctionsImmunohistochemistryRetinaRetinal Rod Photoreceptor CellsVisual PathwaysCalbindin 2ConnexinsGap Junction delta-2 ProteinAII amacrine cellCalretininEccentricityGap junction

Identifiers

PMID31172263
PMCPMC6591202
OpenAlexW2955623649

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.