Evidence map›Paper›PMID 30658859›Full record

ArticleNeuron2019

Functional Synaptic Architecture of Callosal Inputs in Mouse Primary Visual Cortex.

Kuo-Sheng Lee, Kaeli Vandemark, Dávid Mezey, Nicole Shultz, David Fitzpatrick

Abstract read
In one paragraph

Article in Neuron, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Engram mechanisms of memory linking and identity.Nature reviews. Neuroscience · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Two-photon calcium imaging of neuronal activity.Nature reviews. Methods primers · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. Gephyrin-Lacking PV Synapses on Neocortical Pyramidal Neurons.International journal of molecular sciences · 2021
    Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

5 authors.

Kuo-Sheng LeeMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA; Integrative Biology and Neuroscience Graduate Program, Florida Atlantic University, Jupiter, FL 33458, USA; International Max Planck Research School for Brain and Behavior, Florida Atlantic University, Jupiter, FL 33458, USA.
Kaeli VandemarkMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.
Dávid MezeyMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.
Nicole ShultzMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.
David FitzpatrickMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA. Electronic address: david.fitzpatrick@mpfi.org.

Funding

Functional Synaptic Architecture of Visual CortexR01EY006821 · NEI · MAX PLANCK FLORIDA CORPORATION · PI FITZPATRICK, DAVID · 1987 to 2020
$7.2M
NEI NIH HHS R01 EY006821
6 · The paper itself

Abstract

Callosal projections are thought to play a critical role in coordinating neural activity between the cerebral hemispheres in placental mammals, but the rules that govern the arrangement of callosal synapses on the dendrites of their target neurons remain poorly understood. Here we describe a high-throughput method to map the functional organization of callosal connectivity by combining in vivo 3D random-access two-photon calcium imaging of the dendritic spines of single V1 neurons with optogenetic stimulation of the presynaptic neural population in the contralateral hemisphere. We find that callosal-recipient spines are more likely to cluster with non-callosal-recipient spines with similar orientation preference. These observations, based on optogenetic stimulation, were confirmed by direct anatomical visualization of callosal synaptic connections using post hoc expansion microscopy. Our results demonstrate, for the first time, that functional synaptic clustering in a short dendritic segment could play a role in integrating distinct neuronal circuits.

Indexed as

AnimalsCorpus CallosumDendritic SpinesFemaleMiceMice, Inbred C57BLOptogeneticsSynapsesVisual Cortexcorpus callosumdendritic spineexpansion microscopyoptogenetic stimulationvisual cortex

Identifiers

PMID30658859
PMCPMC7012385

What OpenQuestion holds

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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.