Author:
Costantini Irene,Baria Enrico,Sorelli Michele,Matuschke Felix,Giardini Francesco,Menzel Miriam,Mazzamuto Giacomo,Silvestri Ludovico,Cicchi Riccardo,Amunts Katrin,Axer Markus,Pavone Francesco Saverio
Abstract
AbstractAnalyzing 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.
Funder
European Union's Horizon 2020 Framework Programme for Research and Innovation Human Brain Project SGA2
European Union's Horizon 2020 Framework Programme for Research and Innovation Human Brain Project SGA3
Massachusetts General Hospital (The General Hospital Corporation), Athinoula A. Martinos Center, The National Institute of Mental Health
Italian Ministry for Education, University, and Research in the framework of the Eurobioimaging Italian Nodes (ESFRI research infrastructure) - Advanced Light Microscopy Italian Node
”Fondazione CR Firenze”
Publisher
Springer Science and Business Media LLC
Cited by
28 articles.
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