Evidence map›Paper›PMID 36945592›Full record

ArticlebioRxiv : the preprint server for biology2023

An adaptive behavioral control motif mediated by cortical axo-axonic inhibition.

Kanghoon Jung, Minhyeok Chang, André Steinecke, Benjamin Berke, Youngjin Choi, Yasuhiro Oisi, David Fitzpatrick, Hiroki Taniguchi, Hyung-Bae Kwon

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Kanghoon JungDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Minhyeok ChangDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
André SteineckeMax Planck Florida Institute for Neuroscience, Jupiter, Florida 33458, USA.
Benjamin BerkeDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Youngjin ChoiDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Yasuhiro OisiMax Planck Florida Institute for Neuroscience, Jupiter, Florida 33458, USA.
David FitzpatrickMax Planck Florida Institute for Neuroscience, Jupiter, Florida 33458, USA.
Hiroki TaniguchiMax Planck Florida Institute for Neuroscience, Jupiter, Florida 33458, USA.
Hyung-Bae KwonDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Johns Hopkins University · USMax Planck Florida Institute for Neuroscience · US

Funding

Cracking the neuromodulation code at single cell resolutionDP1MH119428 · NIMH · MAX PLANCK FLORIDA CORPORATION · PI KWON, HYUNGBAE · 2018 to 2022
$5.9M
Long-term plasticity expressed in layer 2/3 cortical microcircuitsR01MH107460 · NIMH · MAX PLANCK FLORIDA CORPORATION · PI KWON, HYUNGBAE · 2015 to 2019
$2.3M
Wiring and developmental principles of inhibitory neocortical circuitsR01MH115917 · NIMH · OHIO STATE UNIVERSITY · PI TANIGUCHI, HIROKI · 2018 to 2022
$2.3M
NIMH NIH HHS DP1 MH119428NIMH NIH HHS R01 MH107460NIMH NIH HHS R01 MH115917
6 · The paper itself

Abstract

Neural circuits are reorganized with specificity during learning. Genetically-defined subgroups of inhibitory interneurons are thought to play distinct roles in learning, but heterogeneity within these subgroups has limited our understanding of the scope and nature of their specific contributions to learning. Here we reveal that the chandelier cell (ChC), an interneuron type that specializes in inhibiting the axon-initial segment (AIS) of pyramidal neurons, establishes cortical microcircuits for organizing neural coding through selective axo-axonic synaptic plasticity. We find that organized motor control is mediated by enhanced population coding of direction-tuned premotor neurons, whose tuning is refined through suppression of irrelevant neuronal activity. ChCs are required for learning-dependent refinements via providing selective inhibitory control over pyramidal neurons rather than global suppression. Quantitative analysis on structural plasticity of axo-axonic synapses revealed that ChCs redistributed inhibitory weights to individual pyramidal neurons during learning. These results demonstrate an adaptive logic of the inhibitory circuit motif responsible for organizing distributed neural representations. Thus, ChCs permit efficient cortical computation in a target cell specific manner, which highlights the significance of interneuron diversity.

Identifiers

PMID36945592
PMCPMC10029003
OpenAlexW4323929145

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.