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Microtome-integrated microscope system for high sensitivity tracking of in-resin fluorescence in blocks and ultrathin sections for correlative microscopy

Many areas of biological research demand the combined use of different imaging modalities to cover a wide range of magnifications and measurements or to place fluorescent patterns into an ultrastructural context. A technically difficult problem is the efficient specimen transfer between different im...

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Autores principales: Lemercier, Nicolas, Middel, Volker, Hentsch, Didier, Taubert, Serge, Takamiya, Masanari, Beil, Tanja, Vonesch, Jean-Luc, Baumbach, Tilo, Schultz, Patrick, Antony, Claude, Strähle, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648784/
https://www.ncbi.nlm.nih.gov/pubmed/29051533
http://dx.doi.org/10.1038/s41598-017-13348-6
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author Lemercier, Nicolas
Middel, Volker
Hentsch, Didier
Taubert, Serge
Takamiya, Masanari
Beil, Tanja
Vonesch, Jean-Luc
Baumbach, Tilo
Schultz, Patrick
Antony, Claude
Strähle, Uwe
author_facet Lemercier, Nicolas
Middel, Volker
Hentsch, Didier
Taubert, Serge
Takamiya, Masanari
Beil, Tanja
Vonesch, Jean-Luc
Baumbach, Tilo
Schultz, Patrick
Antony, Claude
Strähle, Uwe
author_sort Lemercier, Nicolas
collection PubMed
description Many areas of biological research demand the combined use of different imaging modalities to cover a wide range of magnifications and measurements or to place fluorescent patterns into an ultrastructural context. A technically difficult problem is the efficient specimen transfer between different imaging modalities without losing the coordinates of the regions-of-interest (ROI). Here, we report a new and highly sensitive integrated system that combines a custom designed microscope with an ultramicrotome for in-resin-fluorescence detection in blocks, ribbons and sections on EM-grids. Although operating with long-distance lenses, this system achieves a very high light sensitivity. Our instrumental set-up and operating workflow are designed to investigate rare events in large tissue volumes. Applications range from studies of individual immune, stem and cancer cells to the investigation of non-uniform subcellular processes. As a use case, we present the ultrastructure of a single membrane repair patch on a muscle fiber in intact muscle in a whole animal context.
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spelling pubmed-56487842017-10-26 Microtome-integrated microscope system for high sensitivity tracking of in-resin fluorescence in blocks and ultrathin sections for correlative microscopy Lemercier, Nicolas Middel, Volker Hentsch, Didier Taubert, Serge Takamiya, Masanari Beil, Tanja Vonesch, Jean-Luc Baumbach, Tilo Schultz, Patrick Antony, Claude Strähle, Uwe Sci Rep Article Many areas of biological research demand the combined use of different imaging modalities to cover a wide range of magnifications and measurements or to place fluorescent patterns into an ultrastructural context. A technically difficult problem is the efficient specimen transfer between different imaging modalities without losing the coordinates of the regions-of-interest (ROI). Here, we report a new and highly sensitive integrated system that combines a custom designed microscope with an ultramicrotome for in-resin-fluorescence detection in blocks, ribbons and sections on EM-grids. Although operating with long-distance lenses, this system achieves a very high light sensitivity. Our instrumental set-up and operating workflow are designed to investigate rare events in large tissue volumes. Applications range from studies of individual immune, stem and cancer cells to the investigation of non-uniform subcellular processes. As a use case, we present the ultrastructure of a single membrane repair patch on a muscle fiber in intact muscle in a whole animal context. Nature Publishing Group UK 2017-10-19 /pmc/articles/PMC5648784/ /pubmed/29051533 http://dx.doi.org/10.1038/s41598-017-13348-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lemercier, Nicolas
Middel, Volker
Hentsch, Didier
Taubert, Serge
Takamiya, Masanari
Beil, Tanja
Vonesch, Jean-Luc
Baumbach, Tilo
Schultz, Patrick
Antony, Claude
Strähle, Uwe
Microtome-integrated microscope system for high sensitivity tracking of in-resin fluorescence in blocks and ultrathin sections for correlative microscopy
title Microtome-integrated microscope system for high sensitivity tracking of in-resin fluorescence in blocks and ultrathin sections for correlative microscopy
title_full Microtome-integrated microscope system for high sensitivity tracking of in-resin fluorescence in blocks and ultrathin sections for correlative microscopy
title_fullStr Microtome-integrated microscope system for high sensitivity tracking of in-resin fluorescence in blocks and ultrathin sections for correlative microscopy
title_full_unstemmed Microtome-integrated microscope system for high sensitivity tracking of in-resin fluorescence in blocks and ultrathin sections for correlative microscopy
title_short Microtome-integrated microscope system for high sensitivity tracking of in-resin fluorescence in blocks and ultrathin sections for correlative microscopy
title_sort microtome-integrated microscope system for high sensitivity tracking of in-resin fluorescence in blocks and ultrathin sections for correlative microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648784/
https://www.ncbi.nlm.nih.gov/pubmed/29051533
http://dx.doi.org/10.1038/s41598-017-13348-6
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