Evidence map›Paper›PMID 36639912›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2023

Quantitative Fluorescence Analysis Reveals Dendrite-Specific Thalamocortical Plasticity in L5 Pyramidal Neurons during Learning.

Ajit Ray, Joseph A Christian, Matthew B Mosso, Eunsol Park, Waja Wegner, Katrin I Willig, Alison L Barth

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2023. 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
2.6field-weighted citation impact, top 10% 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, 24 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Ajit RayDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh Pennsylvania 15213.ORCID 0000-0003-2045-4109
Joseph A ChristianDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh Pennsylvania 15213.
Matthew B MossoDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh Pennsylvania 15213.
Eunsol ParkDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh Pennsylvania 15213.
Waja WegnerOptical Nanoscopy in Neuroscience, Center for Nanoscale Microscopy and Molecular Physiology of the Brain, University Medical Center Göttingen, 37099 Göttingen, Germany.
Katrin I WilligOptical Nanoscopy in Neuroscience, Center for Nanoscale Microscopy and Molecular Physiology of the Brain, University Medical Center Göttingen, 37099 Göttingen, Germany.ORCID 0000-0002-1860-334X
Alison L BarthDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh Pennsylvania 15213 albarth@andrew.cmu.edu.ORCID 0000-0001-7092-1356
Carnegie Mellon University · USUniversitätsmedizin Göttingen · DE

Funding

High Throughput Approaches for Cell-Specific Synapse CharacterizationRF1MH114103 · NIMH · CARNEGIE-MELLON UNIVERSITY · PI BARTH, ALISON L, BRUCHEZ, MARCEL P · 2017 to 2018
$2.5M
Fluorescence-based methods for microconnectivity analysis in neocortexRF1MH129267 · NIMH · CARNEGIE-MELLON UNIVERSITY · PI BARTH, ALISON L · 2022 to 2022
$1.6M
In Vivo Synaptic Imaging in NeocortexR21MH123906 · NIMH · CARNEGIE-MELLON UNIVERSITY · PI BARTH, ALISON L · 2021 to 2022
$408k
NIMH NIH HHS R21 MH123906NIMH NIH HHS RF1 MH114103NIMH NIH HHS RF1 MH129267
6 · The paper itself

Abstract

High-throughput anatomic data can stimulate and constrain new hypotheses about how neural circuits change in response to experience. Here, we use fluorescence-based reagents for presynaptic and postsynaptic labeling to monitor changes in thalamocortical synapses onto different compartments of layer 5 (L5) pyramidal (Pyr) neurons in somatosensory (barrel) cortex from mixed-sex mice during whisker-dependent learning (Audette et al., 2019). Using axonal fills and molecular-genetic tags for synapse identification in fixed tissue from Rbp4-Cre transgenic mice, we found that thalamocortical synapses from the higher-order posterior medial thalamic nucleus showed rapid morphologic changes in both presynaptic and postsynaptic structures at the earliest stages of sensory association training. Detected increases in thalamocortical synaptic size were compartment specific, occurring selectively in the proximal dendrites onto L5 Pyr and not at inputs onto their apical tufts in L1. Both axonal and dendritic changes were transient, normalizing back to baseline as animals became expert in the task. Anatomical measurements were corroborated by electrophysiological recordings at different stages of training. Thus, fluorescence-based analysis of input- and target-specific synapses can reveal compartment-specific changes in synapse properties during learning.

Indexed as

NeuronsPyramidal CellsAnimalsDendritesFluorescenceMiceMice, TransgenicNeuronal PlasticitySomatosensory CortexSynapsesThalamusapical dendriteintrabodieslearningLTPplasticityPOm thalamus

Identifiers

PMID36639912
PMCPMC9888508
OpenAlexW4312132734

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.