A novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughout

Current optical microscope objectives of low magnification have low numerical aperture and therefore have too little depth resolution and discrimination to perform well in confocal and nonlinear microscopy. This is a serious limitation in important areas, including the phenotypic screening of human...

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Main Authors: Gail McConnell, Johanna Trägårdh, Rumelo Amor, John Dempster, Es Reid, William Bradshaw Amos
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2016-09-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/18659
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spelling doaj-e771731c9502434f8bcf423c302fe30c2021-05-05T00:35:52ZengeLife Sciences Publications LtdeLife2050-084X2016-09-01510.7554/eLife.18659A novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughoutGail McConnell0https://orcid.org/0000-0002-7213-0686Johanna Trägårdh1Rumelo Amor2John Dempster3Es Reid4William Bradshaw Amos5Centre for Biophotonics, Strathclyde Institute for Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United KingdomCentre for Biophotonics, Strathclyde Institute for Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United KingdomCentre for Biophotonics, Strathclyde Institute for Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United KingdomCentre for Biophotonics, Strathclyde Institute for Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United KingdomCentre for Biophotonics, Strathclyde Institute for Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United KingdomCentre for Biophotonics, Strathclyde Institute for Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United Kingdom; MRC Laboratory of Molecular Biology, Cambridge, United KingdomCurrent optical microscope objectives of low magnification have low numerical aperture and therefore have too little depth resolution and discrimination to perform well in confocal and nonlinear microscopy. This is a serious limitation in important areas, including the phenotypic screening of human genes in transgenic mice by study of embryos undergoing advanced organogenesis. We have built an optical lens system for 3D imaging of objects up to 6 mm wide and 3 mm thick with depth resolution of only a few microns instead of the tens of microns currently attained, allowing sub-cellular detail to be resolved throughout the volume. We present this lens, called the Mesolens, with performance data and images from biological specimens including confocal images of whole fixed and intact fluorescently-stained 12.5-day old mouse embryos.https://elifesciences.org/articles/18659confocal microscopyembryologyorganogenesis
collection DOAJ
language English
format Article
sources DOAJ
author Gail McConnell
Johanna Trägårdh
Rumelo Amor
John Dempster
Es Reid
William Bradshaw Amos
spellingShingle Gail McConnell
Johanna Trägårdh
Rumelo Amor
John Dempster
Es Reid
William Bradshaw Amos
A novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughout
eLife
confocal microscopy
embryology
organogenesis
author_facet Gail McConnell
Johanna Trägårdh
Rumelo Amor
John Dempster
Es Reid
William Bradshaw Amos
author_sort Gail McConnell
title A novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughout
title_short A novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughout
title_full A novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughout
title_fullStr A novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughout
title_full_unstemmed A novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughout
title_sort novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughout
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2016-09-01
description Current optical microscope objectives of low magnification have low numerical aperture and therefore have too little depth resolution and discrimination to perform well in confocal and nonlinear microscopy. This is a serious limitation in important areas, including the phenotypic screening of human genes in transgenic mice by study of embryos undergoing advanced organogenesis. We have built an optical lens system for 3D imaging of objects up to 6 mm wide and 3 mm thick with depth resolution of only a few microns instead of the tens of microns currently attained, allowing sub-cellular detail to be resolved throughout the volume. We present this lens, called the Mesolens, with performance data and images from biological specimens including confocal images of whole fixed and intact fluorescently-stained 12.5-day old mouse embryos.
topic confocal microscopy
embryology
organogenesis
url https://elifesciences.org/articles/18659
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