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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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 |
work_keys_str_mv |
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