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4D (x-y-z-t) imaging of thick biological samples by means of Two-Photon inverted Selective Plane Illumination Microscopy (2PE-iSPIM)

In the last decade light sheet fluorescence microscopy techniques, such as selective plane illumination microscopy (SPIM), has become a well established method for developmental biology. However, conventional SPIM architectures hardly permit imaging of certain tissues since the common sample mountin...

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Autores principales: Lavagnino, Zeno, Sancataldo, Giuseppe, d’Amora, Marta, Follert, Philipp, De Pietri Tonelli, Davide, Diaspro, Alberto, Cella Zanacchi, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817031/
https://www.ncbi.nlm.nih.gov/pubmed/27033347
http://dx.doi.org/10.1038/srep23923
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author Lavagnino, Zeno
Sancataldo, Giuseppe
d’Amora, Marta
Follert, Philipp
De Pietri Tonelli, Davide
Diaspro, Alberto
Cella Zanacchi, Francesca
author_facet Lavagnino, Zeno
Sancataldo, Giuseppe
d’Amora, Marta
Follert, Philipp
De Pietri Tonelli, Davide
Diaspro, Alberto
Cella Zanacchi, Francesca
author_sort Lavagnino, Zeno
collection PubMed
description In the last decade light sheet fluorescence microscopy techniques, such as selective plane illumination microscopy (SPIM), has become a well established method for developmental biology. However, conventional SPIM architectures hardly permit imaging of certain tissues since the common sample mounting procedure, based on gel embedding, could interfere with the sample morphology. In this work we propose an inverted selective plane microscopy system (iSPIM), based on non-linear excitation, suitable for 3D tissue imaging. First, the iSPIM architecture provides flexibility on the sample mounting, getting rid of the gel-based mounting typical of conventional SPIM, permitting 3D imaging of hippocampal slices from mouse brain. Moreover, all the advantages brought by two photon excitation (2PE) in terms of reduction of scattering effects and contrast improvement are exploited, demonstrating an improved image quality and contrast compared to single photon excitation. The system proposed represents an optimal platform for tissue imaging and it smooths the way to the applicability of light sheet microscopy to a wider range of samples including those that have to be mounted on non-transparent surfaces.
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spelling pubmed-48170312016-04-05 4D (x-y-z-t) imaging of thick biological samples by means of Two-Photon inverted Selective Plane Illumination Microscopy (2PE-iSPIM) Lavagnino, Zeno Sancataldo, Giuseppe d’Amora, Marta Follert, Philipp De Pietri Tonelli, Davide Diaspro, Alberto Cella Zanacchi, Francesca Sci Rep Article In the last decade light sheet fluorescence microscopy techniques, such as selective plane illumination microscopy (SPIM), has become a well established method for developmental biology. However, conventional SPIM architectures hardly permit imaging of certain tissues since the common sample mounting procedure, based on gel embedding, could interfere with the sample morphology. In this work we propose an inverted selective plane microscopy system (iSPIM), based on non-linear excitation, suitable for 3D tissue imaging. First, the iSPIM architecture provides flexibility on the sample mounting, getting rid of the gel-based mounting typical of conventional SPIM, permitting 3D imaging of hippocampal slices from mouse brain. Moreover, all the advantages brought by two photon excitation (2PE) in terms of reduction of scattering effects and contrast improvement are exploited, demonstrating an improved image quality and contrast compared to single photon excitation. The system proposed represents an optimal platform for tissue imaging and it smooths the way to the applicability of light sheet microscopy to a wider range of samples including those that have to be mounted on non-transparent surfaces. Nature Publishing Group 2016-04-01 /pmc/articles/PMC4817031/ /pubmed/27033347 http://dx.doi.org/10.1038/srep23923 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lavagnino, Zeno
Sancataldo, Giuseppe
d’Amora, Marta
Follert, Philipp
De Pietri Tonelli, Davide
Diaspro, Alberto
Cella Zanacchi, Francesca
4D (x-y-z-t) imaging of thick biological samples by means of Two-Photon inverted Selective Plane Illumination Microscopy (2PE-iSPIM)
title 4D (x-y-z-t) imaging of thick biological samples by means of Two-Photon inverted Selective Plane Illumination Microscopy (2PE-iSPIM)
title_full 4D (x-y-z-t) imaging of thick biological samples by means of Two-Photon inverted Selective Plane Illumination Microscopy (2PE-iSPIM)
title_fullStr 4D (x-y-z-t) imaging of thick biological samples by means of Two-Photon inverted Selective Plane Illumination Microscopy (2PE-iSPIM)
title_full_unstemmed 4D (x-y-z-t) imaging of thick biological samples by means of Two-Photon inverted Selective Plane Illumination Microscopy (2PE-iSPIM)
title_short 4D (x-y-z-t) imaging of thick biological samples by means of Two-Photon inverted Selective Plane Illumination Microscopy (2PE-iSPIM)
title_sort 4d (x-y-z-t) imaging of thick biological samples by means of two-photon inverted selective plane illumination microscopy (2pe-ispim)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817031/
https://www.ncbi.nlm.nih.gov/pubmed/27033347
http://dx.doi.org/10.1038/srep23923
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