Evidence map›Paper›PMID 35060903›Full record

ArticleeLife2022

Synaptic connectivity to L2/3 of primary visual cortex measured by two-photon optogenetic stimulation.

Travis A Hage, Alice Bosma-Moody, Christopher A Baker, Megan B Kratz, Luke Campagnola, Tim Jarsky, Hongkui Zeng, Gabe J Murphy

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 76 citations in OpenAlex.

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  16. Exact linear theory of perturbation response in a space- and feature-dependent cortical circuit model.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Review
  18. Patchy harmonic functional connectivity of the mouse auditory cortex.Proceedings of the National Academy of Sciences of the United States of America · 2025
    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

8 authors at 1 institution in 1 country.

Travis A HageAllen Institute for Brain Science, Seattle, United States.ORCID 0000-0002-6125-2768
Alice Bosma-MoodyAllen Institute for Brain Science, Seattle, United States.
Christopher A BakerAllen Institute for Brain Science, Seattle, United States.ORCID 0000-0002-0604-8449
Megan B KratzAllen Institute for Brain Science, Seattle, United States.
Luke CampagnolaAllen Institute for Brain Science, Seattle, United States.
Tim JarskyAllen Institute for Brain Science, Seattle, United States.ORCID 0000-0002-4399-539X
Hongkui ZengAllen Institute for Brain Science, Seattle, United States.ORCID 0000-0002-0326-5878
Gabe J MurphyAllen Institute for Brain Science, Seattle, United States.
Allen Institute for Brain Science · US

Funding

Generation of novel cell type specific mouse genetic toolsU19MH114830 · NIMH · ALLEN INSTITUTE · PI ZENG, HONGKUI · 2017 to 2021
$64.7M
Establishing a Comprehensive and Standardized Cell Type Characterization PlatformU01MH105982 · NIMH · ALLEN INSTITUTE · PI ANDERSON, DAVID J, ZENG, HONGKUI · 2014 to 2016
$5.1M
NIMH NIH HHS U01 MH105982NIMH NIH HHS U19 MH114830
6 · The paper itself

Abstract

Understanding cortical microcircuits requires thorough measurement of physiological properties of synaptic connections formed within and between diverse subclasses of neurons. Towards this goal, we combined spatially precise optogenetic stimulation with multicellular recording to deeply characterize intralaminar and translaminar monosynaptic connections to supragranular (L2/3) neurons in the mouse visual cortex. The reliability and specificity of multiphoton optogenetic stimulation were measured across multiple Cre lines, and measurements of connectivity were verified by comparison to paired recordings and targeted patching of optically identified presynaptic cells. With a focus on translaminar pathways, excitatory and inhibitory synaptic connections from genetically defined presynaptic populations were characterized by their relative abundance, spatial profiles, strength, and short-term dynamics. Consistent with the canonical cortical microcircuit, layer 4 excitatory neurons and interneurons within L2/3 represented the most common sources of input to L2/3 pyramidal cells. More surprisingly, we also observed strong excitatory connections from layer 5 intratelencephalic neurons and potent translaminar inhibition from multiple interneuron subclasses. The hybrid approach revealed convergence to and divergence from excitatory and inhibitory neurons within and across cortical layers. Divergent excitatory connections often spanned hundreds of microns of horizontal space. In contrast, divergent inhibitory connections were more frequently measured from postsynaptic targets near each other.

Indexed as

PhotonsAction PotentialsAnimalsBrainCell LineExcitatory Postsynaptic PotentialsFemaleMaleMiceOptogeneticsPrimary Visual CortexPyramidal CellsReproducibility of ResultsSynapsesSynaptic TransmissionVisual Cortexconnectivitymouseneuroscienceoptogeneticspatch-clampsynapse

Identifiers

PMID35060903
PMCPMC8824465
OpenAlexW4205144568

What OpenQuestion holds

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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.