Evidence map›Paper›PMID 37720921›Full record

ArticleFrontiers in neural circuits2023

Anatomical identification of a corticocortical top-down recipient inhibitory circuitry by enhancer-restricted transsynaptic tracing.

Yusuke Atsumi, Yasuhiro Oisi, Maya Odagawa, Chie Matsubara, Yoshihito Saito, Hiroyuki Uwamori, Kenta Kobayashi, Shigeki Kato, Kazuto Kobayashi, Masanori Murayama

Abstract read
In one paragraph

Article in Frontiers in neural circuits, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Circuit Organization of the Forelimb-Related M2-to-M1 Corticocortical Pathway in the Mouse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  2. Article
  3. 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

10 authors.

Yusuke AtsumiLaboratory for Haptic Perception and Cognitive Physiology, RIKEN Center for Brain Science, Saitama, Japan.
Yasuhiro OisiLaboratory for Haptic Perception and Cognitive Physiology, RIKEN Center for Brain Science, Saitama, Japan.
Maya OdagawaLaboratory for Haptic Perception and Cognitive Physiology, RIKEN Center for Brain Science, Saitama, Japan.
Chie MatsubaraLaboratory for Haptic Perception and Cognitive Physiology, RIKEN Center for Brain Science, Saitama, Japan.
Yoshihito SaitoLaboratory for Haptic Perception and Cognitive Physiology, RIKEN Center for Brain Science, Saitama, Japan.
Hiroyuki UwamoriLaboratory for Haptic Perception and Cognitive Physiology, RIKEN Center for Brain Science, Saitama, Japan.
Kenta KobayashiSection of Viral Vector Development, National Institute for Physiological Sciences, Okazaki-shi, Japan.
Shigeki KatoDepartment of Molecular Genetics, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kazuto KobayashiDepartment of Molecular Genetics, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, Fukushima, Japan.
Masanori MurayamaLaboratory for Haptic Perception and Cognitive Physiology, RIKEN Center for Brain Science, Saitama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the importance of postsynaptic inhibitory circuitry targeted by mid/long-range projections (e.g., top-down projections) in cognitive functions, its anatomical properties, such as laminar profile and neuron type, are poorly understood owing to the lack of efficient tracing methods. To this end, we developed a method that combines conventional adeno-associated virus (AAV)-mediated transsynaptic tracing with a distal-less homeobox (Dlx) enhancer-restricted expression system to label postsynaptic inhibitory neurons. We called this method "Dlx enhancer-restricted Interneuron-SpECific transsynaptic Tracing" (DISECT). We applied DISECT to a top-down corticocortical circuit from the secondary motor cortex (M2) to the primary somatosensory cortex (S1) in wild-type mice. First, we injected AAV1-Cre into the M2, which enabled Cre recombinase expression in M2-input recipient S1 neurons. Second, we injected AAV1-hDlx-flex-green fluorescent protein (GFP) into the S1 to transduce GFP into the postsynaptic inhibitory neurons in a Cre-dependent manner. We succeeded in exclusively labeling the recipient inhibitory neurons in the S1. Laminar profile analysis of the neurons labeled via DISECT indicated that the M2-input recipient inhibitory neurons were distributed in the superficial and deep layers of the S1. This laminar distribution was aligned with the laminar density of axons projecting from the M2. We further classified the labeled neuron types using immunohistochemistry and

Indexed as

InterneuronsNeuronsAnimalsAxonsCognitionDependovirusGreen Fluorescent ProteinsMiceGreen Fluorescent Proteinsanterograde transsynaptic tracingcorticocortical circuitenhancer-based viral vectorsinhibitory neuronstop-down input

Identifiers

PMID37720921
PMCPMC10502327

What Socratic 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 Socratic graph.