Evidence map›Paper›PMID 29089553›Full record

ArticleNature communications2017

Homeostatic plasticity shapes the visual system's first synapse.

Robert E Johnson, Nai-Wen Tien, Ning Shen, James T Pearson, Florentina Soto, Daniel Kerschensteiner

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 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
1.5field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  8. AMIGO1 Promotes Axon Growth and Territory Matching in the Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  9. Retinal Plasticity.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
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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 at 1 institution in 1 country.

Robert E JohnsonDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, Saint Louis, MO, 63110, USA.
Nai-Wen TienDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, Saint Louis, MO, 63110, USA.
Ning ShenDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, Saint Louis, MO, 63110, USA.
James T PearsonDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, Saint Louis, MO, 63110, USA.
Florentina SotoDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, Saint Louis, MO, 63110, USA.
Daniel KerschensteinerDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, Saint Louis, MO, 63110, USA. kerschensteinerd@wustl.edu.
Washington University in St. Louis · US

Funding

SYNAPTIC ORGANIZATION AND VISUAL PROCESSING IN INTERNEURON CIRCUITS OF THE RETINAR01EY026978 · NEI · WASHINGTON UNIVERSITY · PI Daniel Kerschensteiner · 2016 to 2026
$3.8M
Synapse rescue and neuroprotection in the retinaR01EY027411 · NEI · WASHINGTON UNIVERSITY · PI Daniel Kerschensteiner · 2017 to 2026
$3.4M
Neuronal plasticity in retinal circuit development and diseaseR01EY023341 · NEI · WASHINGTON UNIVERSITY · PI KERSCHENSTEINER, DANIEL · 2014 to 2022
$2.8M
NEI NIH HHS R01 EY023341NEI NIH HHS R01 EY026978NEI NIH HHS R01 EY027411
6 · The paper itself

Abstract

Vision in dim light depends on synapses between rods and rod bipolar cells (RBCs). Here, we find that these synapses exist in multiple configurations, in which single release sites of rods are apposed by one to three postsynaptic densities (PSDs). Single RBCs often form multiple PSDs with one rod; and neighboring RBCs share ~13% of their inputs. Rod-RBC synapses develop while ~7% of RBCs undergo programmed cell death (PCD). Although PCD is common throughout the nervous system, its influences on circuit development and function are not well understood. We generate mice in which ~53 and ~93% of RBCs, respectively, are removed during development. In these mice, dendrites of the remaining RBCs expand in graded fashion independent of light-evoked input. As RBC dendrites expand, they form fewer multi-PSD contacts with rods. Electrophysiological recordings indicate that this homeostatic co-regulation of neurite and synapse development preserves retinal function in dim light.

Indexed as

HomeostasisAnimalsAxonsCell CountDendritesLightMice, TransgenicNeuronal PlasticityRetinal Bipolar CellsRetinal Rod Photoreceptor CellsSynapsesVisual Pathways

Identifiers

PMID29089553
PMCPMC5663853
OpenAlexW2765372207

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.