Block face scanning electron microscopy of fluorescently labeled axons without using near infra-red branding

In this article, we describe the method that allows fluorescently tagged structures such as axons to be targeted for electron microscopy (EM) analysis without the need to convert their labels into electron dense stains, introduce any fiducial marks, or image large volumes at high resolution. We opti...

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Main Authors: Maclachlan, C, Sahlender, DA, Hayashi, S, Molnár, Z, Knott, G
Format: Journal article
Language:English
Published: Frontiers Media 2018
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author Maclachlan, C
Sahlender, DA
Hayashi, S
Molnár, Z
Knott, G
author_facet Maclachlan, C
Sahlender, DA
Hayashi, S
Molnár, Z
Knott, G
author_sort Maclachlan, C
collection OXFORD
description In this article, we describe the method that allows fluorescently tagged structures such as axons to be targeted for electron microscopy (EM) analysis without the need to convert their labels into electron dense stains, introduce any fiducial marks, or image large volumes at high resolution. We optimally preserve and stain the brain tissue for ultrastructural analysis and use natural landmarks, such as cell bodies and blood vessels, to locate neurites that had been imaged previously using confocal microscopy. The method relies on low and high magnification views taken with the light microscope, after fixation, to capture information of the tissue structure that can later be used to pinpoint the position of structures of interest in serial EM images. The examples shown here are td Tomato expressing cortico-thalamic axons in the posteromedial nucleus of the mouse thalamus, imaged in fixed tissue with confocal microscopy, and subsequently visualized with serial block-face EM (SBEM) and reconstructed into 3D models for analysis.
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spelling oxford-uuid:fbc78964-17d4-4822-929f-feab3875afa12022-03-27T13:16:18ZBlock face scanning electron microscopy of fluorescently labeled axons without using near infra-red brandingJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:fbc78964-17d4-4822-929f-feab3875afa1EnglishSymplectic Elements at OxfordFrontiers Media2018Maclachlan, CSahlender, DAHayashi, SMolnár, ZKnott, GIn this article, we describe the method that allows fluorescently tagged structures such as axons to be targeted for electron microscopy (EM) analysis without the need to convert their labels into electron dense stains, introduce any fiducial marks, or image large volumes at high resolution. We optimally preserve and stain the brain tissue for ultrastructural analysis and use natural landmarks, such as cell bodies and blood vessels, to locate neurites that had been imaged previously using confocal microscopy. The method relies on low and high magnification views taken with the light microscope, after fixation, to capture information of the tissue structure that can later be used to pinpoint the position of structures of interest in serial EM images. The examples shown here are td Tomato expressing cortico-thalamic axons in the posteromedial nucleus of the mouse thalamus, imaged in fixed tissue with confocal microscopy, and subsequently visualized with serial block-face EM (SBEM) and reconstructed into 3D models for analysis.
spellingShingle Maclachlan, C
Sahlender, DA
Hayashi, S
Molnár, Z
Knott, G
Block face scanning electron microscopy of fluorescently labeled axons without using near infra-red branding
title Block face scanning electron microscopy of fluorescently labeled axons without using near infra-red branding
title_full Block face scanning electron microscopy of fluorescently labeled axons without using near infra-red branding
title_fullStr Block face scanning electron microscopy of fluorescently labeled axons without using near infra-red branding
title_full_unstemmed Block face scanning electron microscopy of fluorescently labeled axons without using near infra-red branding
title_short Block face scanning electron microscopy of fluorescently labeled axons without using near infra-red branding
title_sort block face scanning electron microscopy of fluorescently labeled axons without using near infra red branding
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AT molnarz blockfacescanningelectronmicroscopyoffluorescentlylabeledaxonswithoutusingnearinfraredbranding
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