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Microscopic Optical Projection Tomography In Vivo

We describe a versatile optical projection tomography system for rapid three-dimensional imaging of microscopic specimens in vivo. Our tomographic setup eliminates the in xy and z strongly asymmetric resolution, resulting from optical sectioning in conventional confocal microscopy. It allows for rob...

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Detalles Bibliográficos
Autores principales: Rieckher, Matthias, Birk, Udo Jochen, Meyer, Heiko, Ripoll, Jorge, Tavernarakis, Nektarios
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084718/
https://www.ncbi.nlm.nih.gov/pubmed/21559481
http://dx.doi.org/10.1371/journal.pone.0018963
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author Rieckher, Matthias
Birk, Udo Jochen
Meyer, Heiko
Ripoll, Jorge
Tavernarakis, Nektarios
author_facet Rieckher, Matthias
Birk, Udo Jochen
Meyer, Heiko
Ripoll, Jorge
Tavernarakis, Nektarios
author_sort Rieckher, Matthias
collection PubMed
description We describe a versatile optical projection tomography system for rapid three-dimensional imaging of microscopic specimens in vivo. Our tomographic setup eliminates the in xy and z strongly asymmetric resolution, resulting from optical sectioning in conventional confocal microscopy. It allows for robust, high resolution fluorescence as well as absorption imaging of live transparent invertebrate animals such as C. elegans. This system offers considerable advantages over currently available methods when imaging dynamic developmental processes and animal ageing; it permits monitoring of spatio-temporal gene expression and anatomical alterations with single-cell resolution, it utilizes both fluorescence and absorption as a source of contrast, and is easily adaptable for a range of small model organisms.
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spelling pubmed-30847182011-05-10 Microscopic Optical Projection Tomography In Vivo Rieckher, Matthias Birk, Udo Jochen Meyer, Heiko Ripoll, Jorge Tavernarakis, Nektarios PLoS One Research Article We describe a versatile optical projection tomography system for rapid three-dimensional imaging of microscopic specimens in vivo. Our tomographic setup eliminates the in xy and z strongly asymmetric resolution, resulting from optical sectioning in conventional confocal microscopy. It allows for robust, high resolution fluorescence as well as absorption imaging of live transparent invertebrate animals such as C. elegans. This system offers considerable advantages over currently available methods when imaging dynamic developmental processes and animal ageing; it permits monitoring of spatio-temporal gene expression and anatomical alterations with single-cell resolution, it utilizes both fluorescence and absorption as a source of contrast, and is easily adaptable for a range of small model organisms. Public Library of Science 2011-04-29 /pmc/articles/PMC3084718/ /pubmed/21559481 http://dx.doi.org/10.1371/journal.pone.0018963 Text en Rieckher et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rieckher, Matthias
Birk, Udo Jochen
Meyer, Heiko
Ripoll, Jorge
Tavernarakis, Nektarios
Microscopic Optical Projection Tomography In Vivo
title Microscopic Optical Projection Tomography In Vivo
title_full Microscopic Optical Projection Tomography In Vivo
title_fullStr Microscopic Optical Projection Tomography In Vivo
title_full_unstemmed Microscopic Optical Projection Tomography In Vivo
title_short Microscopic Optical Projection Tomography In Vivo
title_sort microscopic optical projection tomography in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084718/
https://www.ncbi.nlm.nih.gov/pubmed/21559481
http://dx.doi.org/10.1371/journal.pone.0018963
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AT tavernarakisnektarios microscopicopticalprojectiontomographyinvivo