Evidence map›Paper›PMID 31554841›Full record

ArticleScientific reports2019

Multifaceted Changes in Synaptic Composition and Astrocytic Involvement in a Mouse Model of Fragile X Syndrome.

Anish K Simhal, Yi Zuo, Marc M Perez, Daniel V Madison, Guillermo Sapiro, Kristina D Micheva

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. 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
2.3field-weighted citation impact, top 11% 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.

  1. Astrocyte TrkB.T1 Deficiency Disrupts Glutamatergic Synaptogenesis and Astrocyte-Synapse Interactions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  9. Emerging Role of Neuron-Glia in Neurological Disorders: At a Glance.Oxidative medicine and cellular longevity · 2022
    Review
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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

6 authors at 3 institutions in 1 country.

Anish K SimhalDepartment of Electrical Engineering, Duke University, Durham, USA. aksimhal@gmail.com.ORCID http://orcid.org/0000-0001-7848-3565
Yi ZuoDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, USA.ORCID http://orcid.org/0000-0001-9020-0003
Marc M PerezDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, USA.
Daniel V MadisonDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, USA.
Guillermo SapiroDepartment of Electrical Engineering, Duke University, Durham, USA.
Kristina D MichevaDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, USA.
Stanford University · USDuke University · USUniversity of California, Santa Cruz · US

Funding

Synaptomes of Mouse and ManR01NS092474 · NINDS · ALLEN INSTITUTE · PI BURNS, RANDAL, SMITH, STEPHEN J · 2014 to 2018
$8.7M
Single synapse analysis of synaptic plasticity by combining electrophysiology and array tomographyR01MH111768 · NIMH · STANFORD UNIVERSITY · PI MADISON, VERNON DANIEL · 2017 to 2021
$2.9M
Dynamics and molecular mechanism of synaptic connectivity change during learningR01MH104227 · NIMH · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI ZUO, YI · 2014 to 2018
$2.1M
Contribution of astrocytes to the Fragile X SyndromeR01MH109475 · NIMH · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI ZUO, YI · 2016 to 2020
$2.0M
Axonal myelination of interneurons in cortex: functional significance and plasticityR01NS094499 · NINDS · STANFORD UNIVERSITY · PI MADISON, VERNON DANIEL · 2016 to 2020
$1.7M
NIMH NIH HHS R01 MH104227NIMH NIH HHS R01 MH109475NIMH NIH HHS R01 MH111768NINDS NIH HHS R01 NS092474NINDS NIH HHS R01 NS094499U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01MH104227
6 · The paper itself

Abstract

Fragile X Syndrome (FXS), a common inheritable form of intellectual disability, is known to alter neocortical circuits. However, its impact on the diverse synapse types comprising these circuits, or on the involvement of astrocytes, is not well known. We used immunofluorescent array tomography to quantify different synaptic populations and their association with astrocytes in layers 1 through 4 of the adult somatosensory cortex of a FXS mouse model, the FMR1 knockout mouse. The collected multi-channel data contained approximately 1.6 million synapses which were analyzed using a probabilistic synapse detector. Our study reveals complex, synapse-type and layer specific changes in the neocortical circuitry of FMR1 knockout mice. We report an increase of small glutamatergic VGluT1 synapses in layer 4 accompanied by a decrease in large VGluT1 synapses in layers 1 and 4. VGluT2 synapses show a rather consistent decrease in density in layers 1 and 2/3. In all layers, we observe the loss of large inhibitory synapses. Lastly, astrocytic association of excitatory synapses decreases. The ability to dissect the circuit deficits by synapse type and astrocytic involvement will be crucial for understanding how these changes affect circuit function, and ultimately defining targets for therapeutic intervention.

Indexed as

AnimalsAstrocytesBrainDisease Models, AnimalFemaleFluorescent Antibody TechniqueFragile X SyndromeFunctional NeuroimagingMagnetic Resonance ImagingMaleMiceMice, Inbred C57BLMice, KnockoutSomatosensory CortexSynapsesTomographySlc17a6 protein, mouseSlc17a7 protein, mouseVesicular Glutamate Transport Protein 1Vesicular Glutamate Transport Protein 2

Identifiers

PMID31554841
PMCPMC6761194
OpenAlexW2975677607

What OpenQuestion holds

Textmetadata
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.