Evidence map›Paper›PMID 24966302›Full record

ArticleJournal of neurophysiology2014

Prolonged synaptic currents increase relay neuron firing at the developing retinogeniculate synapse.

Jessica L Hauser, Xiaojin Liu, Elizabeth Y Litvina, Chinfei Chen

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Reciprocal interaction between cortical SST and PV interneurons in top-down regulation of retinothalamic refinement.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Activity-induced MeCP2 phosphorylation regulates retinogeniculate synapse refinement.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Article
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  9. Article
  10. Distinct functional developments of surviving and eliminated presynaptic terminals.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Article
  12. Review
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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

4 authors at 2 institutions in 1 country.

Jessica L HauserDepartment of Neurology, F. M. Kirby Neurobiology Center, Children's Hospital, Boston, Massachusetts; and Program in Neuroscience, Harvard Medical School, Boston, Massachusetts.
Xiaojin LiuDepartment of Neurology, F. M. Kirby Neurobiology Center, Children's Hospital, Boston, Massachusetts; and Program in Neuroscience, Harvard Medical School, Boston, Massachusetts.
Elizabeth Y LitvinaDepartment of Neurology, F. M. Kirby Neurobiology Center, Children's Hospital, Boston, Massachusetts; and Program in Neuroscience, Harvard Medical School, Boston, Massachusetts.
Chinfei ChenDepartment of Neurology, F. M. Kirby Neurobiology Center, Children's Hospital, Boston, Massachusetts; and Program in Neuroscience, Harvard Medical School, Boston, Massachusetts chinfei.chen@childrens.harvard.edu.
Harvard University · USBoston Children's Hospital · US

Funding

SYNAPTIC MECHANISMS IN HIPPOCAMPAL EPILEPTOGENESISP30HD018655 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI POMEROY, SCOTT LOREN · 1985 to 2015
$26.2M
PHD TRAINING IN NEUROSCIENCET32MH020017 · NIMH · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI JOHN ASSAD · 1997 to 2026
$15.8M
Short-term plasticity of the retinogeniculate synapseR01EY013613 · NEI · CHILDREN'S HOSPITAL BOSTON · PI Chinfei Chen · 2003 to 2026
$10.3M
RESEARCH TRAINING IN VISUAL NEUROSCIENCET32EY007110 · NEI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BORN, RICHARD T · 1988 to 2023
$4.1M
NEI NIH HHS R01 EY013613NEI NIH HHS R01-EY-013613NEI NIH HHS T32 EY-007110NEI NIH HHS T32 EY007110NICHD NIH HHS P01-HD-18655NICHD NIH HHS P30 HD018655NIMH NIH HHS 5T32-MH-020017NIMH NIH HHS T32 MH020017
6 · The paper itself

Abstract

The retinogeniculate synapse, the connection between retinal ganglion cells (RGC) and thalamic relay neurons, undergoes robust changes in connectivity over development. This process of synapse elimination and strengthening of remaining inputs is thought to require synapse specificity. Here we show that glutamate spillover and asynchronous release are prominent features of retinogeniculate synaptic transmission during this period. The immature excitatory postsynaptic currents exhibit a slow decay time course that is sensitive to low-affinity glutamate receptor antagonists and extracellular calcium concentrations, consistent with glutamate spillover. Furthermore, we uncover and characterize a novel, purely spillover-mediated AMPA receptor current from immature relay neurons. The isolation of this current strongly supports the presence of spillover between boutons of different RGCs. In addition, fluorescence measurements of presynaptic calcium transients suggest that prolonged residual calcium contributes to both glutamate spillover and asynchronous release. These data indicate that, during development, far more RGCs contribute to relay neuron firing than would be expected based on predictions from anatomy alone.

Indexed as

AnimalsCalciumExcitatory Postsynaptic PotentialsGeniculate BodiesGlutamatesMice, Inbred C57BLNeural PathwaysNeuronsReceptors, AMPAReceptors, N-Methyl-D-AspartateRetinal Ganglion CellsSynapsesCalciumGlutamatesReceptors, AMPAReceptors, N-Methyl-D-Aspartateasynchronous releasedevelopmentglutamate spilloverretinogeniculate synapsevisual system

Identifiers

PMID24966302
PMCPMC4157180
OpenAlexW2056255073

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.