Evidence map›Paper›PMID 21471382›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Functional elimination of excitatory feedforward inputs underlies developmental refinement of visual receptive fields in zebrafish.

Min Zhang, Yan Liu, Sheng-zhi Wang, Wen Zhong, Bao-hua Liu, Huizhong Whit Tao

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. 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
2.2field-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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Functional Integration of Newborn Neurons in the Zebrafish Optic Tectum.Frontiers in cell and developmental biology · 2019
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Generation of intensity selectivity by differential synaptic tuning: fast-saturating excitation but slow-saturating inhibition.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  19. A competition-based mechanism mediates developmental refinement of tectal neuron receptive fields.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  20. Broadening of inhibitory tuning underlies contrast-dependent sharpening of orientation selectivity in mouse visual cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    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

6 authors at 3 institutions in 3 countries.

Min ZhangZilkha Neurogenetic Institute, Graduate Program, Keck School of Medicine, University of Southern California, Los Angeles, California 90089, USA.
Yan Liu
Sheng-zhi Wang
Wen Zhong
Bao-hua Liu
Huizhong Whit Tao
Guangdong Provincial Hospital of Traditional Chinese Medicine · CNInstitute of Cell Biology and Neurobiology · ITUniversity of Southern California · US

Funding

Processing and transformation of visual signals in the superior colliculusR01EY019049 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TAO, HUIZHONG WHIT · 2008 to 2025
$9.2M
NEI NIH HHS EY019049NEI NIH HHS R01 EY019049
6 · The paper itself

Abstract

In many sensory systems, receptive fields (RFs) measured by spike responses undergo progressive refinement during development. It has been proposed that elimination of excitatory synaptic inputs underlies such functional refinement. However, despite many extracellular recording and anatomical studies, direct in vivo intracellular evidence has remained limited. In this study, by cell-attached recordings in the developing optic tectum of zebrafish, we found that during a short period after the initial formation of retinotectal synapses, spike visual RFs of tectal neurons underwent a two-stage developmental modulation: from an initial expansion to a later refinement. Whole-cell voltage-clamp recordings revealed that the underlying excitatory synaptic RF exhibited a similar developmental progression, with its spatial extent first increased and then reduced, and its spatial tuning profile gradually sharpened. The inhibitory RF was initially larger than the excitatory RF but became matched with the excitatory RF at later stages. Simulation with the integrate-and-fire neuron model suggested that the developmental changes of excitatory RFs primarily accounted for the initial enlargement and later refinement of spike RFs, whereas inhibitory inputs generally reduced the size of the spike RF without affecting its developmental progression. In addition, spike RF of individual retinal ganglion cells did not significantly change in size during the same period, and the spatial extent and tuning profile of the tectal excitatory RF barely changed after intratectal excitatory connections were silenced. Together, our results demonstrate that the functional refinement of tectal visual RFs results primarily from a selective elimination of feedforward retinotectal inputs.

Indexed as

Action PotentialsAnalysis of VarianceAnimalsBiophysicsBrain MappingComputer SimulationElectric StimulationFunctional LateralityGABA AntagonistsModels, NeurologicalMorpholinesNerve NetNeural InhibitionPatch-Clamp TechniquesPhotic StimulationRetinal Ganglion CellsGABA AntagonistsMorpholines(+)-(S)-5,5-dimethylmorpholinyl-2-acetic acid

Identifiers

PMID21471382
PMCPMC3095389
OpenAlexW2086424202

What OpenQuestion holds

Textmetadata
LicenceTDM
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.