Evidence map›Paper›PMID 29352045›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

Eliminating Glutamatergic Input onto Horizontal Cells Changes the Dynamic Range and Receptive Field Organization of Mouse Retinal Ganglion Cells.

Sebastian Ströh, Christian Puller, Sebastian Swirski, Maj-Britt Hölzel, Lea I S van der Linde, Jasmin Segelken, Konrad Schultz, Christoph Block, Hannah Monyer, Klaus Willecke and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  10. TDP43 pathology in chronic traumatic encephalopathy retinas.Acta neuropathologica communications · 2023
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  17. Synchronous inhibitory pathways create both efficiency and diversity in the retina.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

14 authors at 7 institutions in 5 countries.

Sebastian StröhDepartments of Neurobiology.ORCID 0000-0001-8128-2617
Christian PullerVisual Neuroscience.
Sebastian SwirskiDepartments of Neurobiology.ORCID 0000-0002-6793-3070
Maj-Britt HölzelNeurosensorics.
Lea I S van der LindeNeurosensorics.ORCID 0000-0003-3196-0007
Jasmin SegelkenDepartments of Neurobiology.ORCID 0000-0002-0650-6729
Konrad SchultzDepartments of Neurobiology.
Christoph BlockVisual Neuroscience.
Hannah MonyerGerman Cancer Research Center (DKFZ), 69120 Heidelberg, Germany, and.
Klaus WilleckeLife and Medical Sciences Institute, University of Bonn, 53115 Bonn, Germany.
Reto WeilerDepartments of Neurobiology.ORCID 0000-0003-0744-5128
Martin GreschnerVisual Neuroscience.
Ulrike Janssen-BienholdDepartments of Neurobiology.ORCID 0000-0002-5059-6477
Karin DedekDepartments of Neurobiology, karin.dedek@uni-oldenburg.de.ORCID 0000-0003-1490-0141
Carl von Ossietzky Universität Oldenburg · DECenter for Visual Communication (United States) · USNanobiosensorics Laboratory · HUGerman Cancer Research Center · DEInstitute of Human Genetics · PLInstitute of Neurobiology · BGUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the mammalian retina, horizontal cells receive glutamatergic inputs from many rod and cone photoreceptors and return feedback signals to them, thereby changing photoreceptor glutamate release in a light-dependent manner. Horizontal cells also provide feedforward signals to bipolar cells. It is unclear, however, how horizontal cell signals also affect the temporal, spatial, and contrast tuning in retinal output neurons, the ganglion cells. To study this, we generated a genetically modified mouse line in which we eliminated the light dependency of feedback by deleting glutamate receptors from mouse horizontal cells. This genetic modification allowed us to investigate the impact of horizontal cells on ganglion cell signaling independent of the actual mode of feedback in the outer retina and without pharmacological manipulation of signal transmission. In control and genetically modified mice (both sexes), we recorded the light responses of transient OFF-α retinal ganglion cells in the intact retina. Excitatory postsynaptic currents (EPSCs) were reduced and the cells were tuned to lower temporal frequencies and higher contrasts, presumably because photoreceptor output was attenuated. Moreover, receptive fields of recorded cells showed a significantly altered surround structure. Our data thus suggest that horizontal cells are responsible for adjusting the dynamic range of retinal ganglion cells and, together with amacrine cells, contribute to the center/surround organization of ganglion cell receptive fields in the mouse.

Indexed as

AnimalsFemaleGlutamineMaleMiceMice, TransgenicRetinal Ganglion CellsRetinal Horizontal CellsSynaptic TransmissionGlutaminegain controlganglion cellsglutamate receptorhorizontal cellsreceptive fieldretina

Identifiers

PMID29352045
PMCPMC6705883
OpenAlexW2783679394

What OpenQuestion holds

Textmetadata
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.