Evidence map›Paper›PMID 29966021›Full record

ArticlePloS one2018

The effects of aging on neuropil structure in mouse somatosensory cortex-A 3D electron microscopy analysis of layer 1.

Corrado Calì, Marta Wawrzyniak, Carlos Becker, Bohumil Maco, Marco Cantoni, Anne Jorstad, Biagio Nigro, Federico Grillo, Vincenzo De Paola, Pascal Fua and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 76 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

11 authors at 4 institutions in 4 countries.

Corrado CalìBioEM Facility, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Marta WawrzyniakBioEPIX, XLI M, Faculty of Science and Technology, University of Limoges, Limoges, France.
Carlos BeckerComputer Vision Laboratory, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Bohumil MacoBioEM Facility, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Marco CantoniCentre for Electron Microscopy, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Anne JorstadComputer Vision Laboratory, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Biagio NigroBioEM Facility, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Federico GrilloMRC Centre for Developmental Neurobiology, King's College London, New Hunt's House Guy's Campus, London, United Kingdom.
Vincenzo De PaolaMRC Clinical Science Centre, Faculty of Medicine, Imperial College London, London, United Kingdom.
Pascal FuaComputer Vision Laboratory, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Graham William KnottBioEM Facility, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
École Polytechnique Fédérale de Lausanne · CHImperial College London · GBKing's College London · GBUniversité de Limoges · FR

Funding

Medical Research Council MC_U120088464
6 · The paper itself

Abstract

This study has used dense reconstructions from serial EM images to compare the neuropil ultrastructure and connectivity of aged and adult mice. The analysis used models of axons, dendrites, and their synaptic connections, reconstructed from volumes of neuropil imaged in layer 1 of the somatosensory cortex. This shows the changes to neuropil structure that accompany a general loss of synapses in a well-defined brain region. The loss of excitatory synapses was balanced by an increase in their size such that the total amount of synaptic surface, per unit length of axon, and per unit volume of neuropil, stayed the same. There was also a greater reduction of inhibitory synapses than excitatory, particularly those found on dendritic spines, resulting in an increase in the excitatory/inhibitory balance. The close correlations, that exist in young and adult neurons, between spine volume, bouton volume, synaptic size, and docked vesicle numbers are all preserved during aging. These comparisons display features that indicate a reduced plasticity of cortical circuits, with fewer, more transient, connections, but nevertheless an enhancement of the remaining connectivity that compensates for a generalized synapse loss.

Indexed as

AgingAnimalsAxonsHumansImaging, Three-DimensionalMiceMicroscopy, ElectronNeuronsNeuropilSomatosensory CortexSynapses

Identifiers

PMID29966021
PMCPMC6028106
OpenAlexW2810169789

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.