Evidence map›Paper›PMID 33850168›Full record

ArticleScientific reports2021

Autofluorescence enhancement for label-free imaging of myelinated fibers in mammalian brains.

Irene Costantini, Enrico Baria, Michele Sorelli, Felix Matuschke, Francesco Giardini, Miriam Menzel, Giacomo Mazzamuto, Ludovico Silvestri, Riccardo Cicchi, Katrin Amunts and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
7.5field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 43 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

12 authors at 3 institutions in 2 countries.

Irene CostantiniEuropean Laboratory for Non-Linear Spectroscopy, University of Florence, Florence, Italy. costantini@lens.unifi.it.
Enrico BariaEuropean Laboratory for Non-Linear Spectroscopy, University of Florence, Florence, Italy.
Michele SorelliEuropean Laboratory for Non-Linear Spectroscopy, University of Florence, Florence, Italy.
Felix MatuschkeInstitute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.
Francesco GiardiniEuropean Laboratory for Non-Linear Spectroscopy, University of Florence, Florence, Italy.
Miriam MenzelInstitute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.
Giacomo MazzamutoEuropean Laboratory for Non-Linear Spectroscopy, University of Florence, Florence, Italy.
Ludovico SilvestriEuropean Laboratory for Non-Linear Spectroscopy, University of Florence, Florence, Italy.
Riccardo CicchiEuropean Laboratory for Non-Linear Spectroscopy, University of Florence, Florence, Italy.
Katrin AmuntsInstitute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.
Markus AxerInstitute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich, Germany.
Francesco Saverio PavoneEuropean Laboratory for Non-Linear Spectroscopy, University of Florence, Florence, Italy.
University of Florence · ITForschungszentrum Jülich · DENational Research Council · IT

Funding

Imaging and Analysis Techniques to Construct a Cell Census Atlas of the Human Brain Admin SupplementU01MH117023 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI BOAS, DAVID A, FISCHL, BRUCE · 2018 to 2022
$7.6M
NIMH NIH HHS U01 MH117023
6 · The paper itself

Abstract

Analyzing the structure of neuronal fibers with single axon resolution in large volumes is a challenge in connectomics. Different technologies try to address this goal; however, they are limited either by the ineffective labeling of the fibers or in the achievable resolution. The possibility of discriminating between different adjacent myelinated axons gives the opportunity of providing more information about the fiber composition and architecture within a specific area. Here, we propose MAGIC (Myelin Autofluorescence imaging by Glycerol Induced Contrast enhancement), a tissue preparation method to perform label-free fluorescence imaging of myelinated fibers that is user friendly and easy to handle. We exploit the high axial and radial resolution of two-photon fluorescence microscopy (TPFM) optical sectioning to decipher the mixture of various fiber orientations within the sample of interest. We demonstrate its broad applicability by performing mesoscopic reconstruction at a sub-micron resolution of mouse, rat, monkey, and human brain samples and by quantifying the different fiber organization in control and Reeler mouse's hippocampal sections. Our study provides a novel method for 3D label-free imaging of nerve fibers in fixed samples at high resolution, below micrometer level, that overcomes the limitation related to the myelinated axons exogenous labeling, improving the possibility of analyzing brain connectivity.

Indexed as

BrainNerve Fibers, MyelinatedAnimalsAxonsHippocampusHumansImaging, Three-DimensionalMiceMicroscopy, Fluorescence, MultiphotonMyelin SheathOptical ImagingRats

Identifiers

PMID33850168
PMCPMC8044204
OpenAlexW3156822836

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.