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Dual-color deep-tissue three-photon microscopy with a multiband infrared laser

Multiphoton microscopy combined with genetically encoded fluorescent indicators is a central tool in biology. Three-photon (3P) microscopy with excitation in the short-wavelength infrared (SWIR) water transparency bands at 1.3 and 1.7 µm opens up new opportunities for deep-tissue imaging. However, n...

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Autores principales: Guesmi, Khmaies, Abdeladim, Lamiae, Tozer, Samuel, Mahou, Pierre, Kumamoto, Takuma, Jurkus, Karolis, Rigaud, Philippe, Loulier, Karine, Dray, Nicolas, Georges, Patrick, Hanna, Marc, Livet, Jean, Supatto, Willy, Beaurepaire, Emmanuel, Druon, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107000/
https://www.ncbi.nlm.nih.gov/pubmed/30839589
http://dx.doi.org/10.1038/s41377-018-0012-2
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author Guesmi, Khmaies
Abdeladim, Lamiae
Tozer, Samuel
Mahou, Pierre
Kumamoto, Takuma
Jurkus, Karolis
Rigaud, Philippe
Loulier, Karine
Dray, Nicolas
Georges, Patrick
Hanna, Marc
Livet, Jean
Supatto, Willy
Beaurepaire, Emmanuel
Druon, Frédéric
author_facet Guesmi, Khmaies
Abdeladim, Lamiae
Tozer, Samuel
Mahou, Pierre
Kumamoto, Takuma
Jurkus, Karolis
Rigaud, Philippe
Loulier, Karine
Dray, Nicolas
Georges, Patrick
Hanna, Marc
Livet, Jean
Supatto, Willy
Beaurepaire, Emmanuel
Druon, Frédéric
author_sort Guesmi, Khmaies
collection PubMed
description Multiphoton microscopy combined with genetically encoded fluorescent indicators is a central tool in biology. Three-photon (3P) microscopy with excitation in the short-wavelength infrared (SWIR) water transparency bands at 1.3 and 1.7 µm opens up new opportunities for deep-tissue imaging. However, novel strategies are needed to enable in-depth multicolor fluorescence imaging and fully develop such an imaging approach. Here, we report on a novel multiband SWIR source that simultaneously emits ultrashort pulses at 1.3 and 1.7 µm that has characteristics optimized for 3P microscopy: sub-70 fs duration, 1.25 MHz repetition rate, and µJ-range pulse energy. In turn, we achieve simultaneous 3P excitation of green fluorescent protein (GFP) and red fluorescent proteins (mRFP, mCherry, tdTomato) along with third-harmonic generation. We demonstrate in-depth dual-color 3P imaging in a fixed mouse brain, chick embryo spinal cord, and live adult zebrafish brain, with an improved signal-to-background ratio compared to multicolor two-photon imaging. This development opens the way towards multiparametric imaging deep within scattering tissues.
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spelling pubmed-61070002018-08-30 Dual-color deep-tissue three-photon microscopy with a multiband infrared laser Guesmi, Khmaies Abdeladim, Lamiae Tozer, Samuel Mahou, Pierre Kumamoto, Takuma Jurkus, Karolis Rigaud, Philippe Loulier, Karine Dray, Nicolas Georges, Patrick Hanna, Marc Livet, Jean Supatto, Willy Beaurepaire, Emmanuel Druon, Frédéric Light Sci Appl Article Multiphoton microscopy combined with genetically encoded fluorescent indicators is a central tool in biology. Three-photon (3P) microscopy with excitation in the short-wavelength infrared (SWIR) water transparency bands at 1.3 and 1.7 µm opens up new opportunities for deep-tissue imaging. However, novel strategies are needed to enable in-depth multicolor fluorescence imaging and fully develop such an imaging approach. Here, we report on a novel multiband SWIR source that simultaneously emits ultrashort pulses at 1.3 and 1.7 µm that has characteristics optimized for 3P microscopy: sub-70 fs duration, 1.25 MHz repetition rate, and µJ-range pulse energy. In turn, we achieve simultaneous 3P excitation of green fluorescent protein (GFP) and red fluorescent proteins (mRFP, mCherry, tdTomato) along with third-harmonic generation. We demonstrate in-depth dual-color 3P imaging in a fixed mouse brain, chick embryo spinal cord, and live adult zebrafish brain, with an improved signal-to-background ratio compared to multicolor two-photon imaging. This development opens the way towards multiparametric imaging deep within scattering tissues. Nature Publishing Group UK 2018-06-06 /pmc/articles/PMC6107000/ /pubmed/30839589 http://dx.doi.org/10.1038/s41377-018-0012-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Comemons 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
Guesmi, Khmaies
Abdeladim, Lamiae
Tozer, Samuel
Mahou, Pierre
Kumamoto, Takuma
Jurkus, Karolis
Rigaud, Philippe
Loulier, Karine
Dray, Nicolas
Georges, Patrick
Hanna, Marc
Livet, Jean
Supatto, Willy
Beaurepaire, Emmanuel
Druon, Frédéric
Dual-color deep-tissue three-photon microscopy with a multiband infrared laser
title Dual-color deep-tissue three-photon microscopy with a multiband infrared laser
title_full Dual-color deep-tissue three-photon microscopy with a multiband infrared laser
title_fullStr Dual-color deep-tissue three-photon microscopy with a multiband infrared laser
title_full_unstemmed Dual-color deep-tissue three-photon microscopy with a multiband infrared laser
title_short Dual-color deep-tissue three-photon microscopy with a multiband infrared laser
title_sort dual-color deep-tissue three-photon microscopy with a multiband infrared laser
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107000/
https://www.ncbi.nlm.nih.gov/pubmed/30839589
http://dx.doi.org/10.1038/s41377-018-0012-2
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