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Intravital Deep-Tumor Single-Beam 2-, 3- and 4-Photon Microscopy

View ORCID ProfileGert-Jan Bakker, Sarah Weischer, Judith Heidelin, Volker Andresen, Marcus Beutler, View ORCID ProfilePeter Friedl
doi: https://doi.org/10.1101/2020.09.29.312827
Gert-Jan Bakker
1Department of Cell Biology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, 6525 GA Nijmegen, The Netherlands
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  • For correspondence: gert-jan.bakker@radboudumc.nl peter.friedl@radboudumc.nl
Sarah Weischer
1Department of Cell Biology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, 6525 GA Nijmegen, The Netherlands
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Judith Heidelin
2LaVision BioTec GmbH, a Miltenyi Biotec company, 33617 Bielefeld, Germany
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Volker Andresen
2LaVision BioTec GmbH, a Miltenyi Biotec company, 33617 Bielefeld, Germany
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Marcus Beutler
3APE Angewandte Physik & Elektronik GmbH, 13053 Berlin, Germany
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Peter Friedl
1Department of Cell Biology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, 6525 GA Nijmegen, The Netherlands
4David H. Koch Center for Applied Genitourinary Cancers, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA
5Cancer Genomics Centre, 3584 CG Utrecht, The Netherlands
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  • For correspondence: gert-jan.bakker@radboudumc.nl peter.friedl@radboudumc.nl
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Abstract

Three-photon excitation has recently been introduced to perform intravital microscopy in deep, previously inaccessible layers of the brain. The applicability of deep-tissue three-photon excitation in more heterogeneously structured, dense tissue types remains, however, unclear. Here we show that in tumors and bone, high-pulse-energy low-duty-cycle infrared excitation near 1300 and 1700 nm enables two-up to fourfold increased tissue penetration compared to conventional 2-photon excitation. Using a single laser line, simultaneous 2-, 3- and 4-photon processes are effectively induced, enabling the simultaneous detection of blue to far-red fluorescence together with second and third harmonic generation. This enables subcellular resolution at power densities in the focus that are not phototoxic to live cells and without color aberration. Thus, infrared high-pulse-energy low-duty-cycle excitation advances deep intravital microscopy in strongly scattering tissue and, in a single scan, delivers rich multi-parameter datasets from cells and complex organ structures.

Competing Interest Statement

Gert-Jan Bakker, Sarah Weischer and Peter Friedl declare no conflicts of interest. Marcus Beutler has a current employment at APE Angewandte Physik & Elektronik GmbH, which produces the AVUS SP as a commercial product. Judith Heidelin and Volker Andresen are currently employed by LaVision BioTec GmbH and explore implementation of high-pulse-energy low-duty-cycle light sources as a microscopy product line.

Footnotes

  • Email addresses co-authors: Sarah Weischer: sarah.weischer{at}radboudumc.nl, Judith Heidelin: heidelin{at}lavisionbiotec.de, Volker Andresen: andresen{at}lavisionbiotec.de, Marcus Beutler: marcus_beutler{at}ape-berlin.de.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted September 30, 2020.
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Intravital Deep-Tumor Single-Beam 2-, 3- and 4-Photon Microscopy
Gert-Jan Bakker, Sarah Weischer, Judith Heidelin, Volker Andresen, Marcus Beutler, Peter Friedl
bioRxiv 2020.09.29.312827; doi: https://doi.org/10.1101/2020.09.29.312827
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Intravital Deep-Tumor Single-Beam 2-, 3- and 4-Photon Microscopy
Gert-Jan Bakker, Sarah Weischer, Judith Heidelin, Volker Andresen, Marcus Beutler, Peter Friedl
bioRxiv 2020.09.29.312827; doi: https://doi.org/10.1101/2020.09.29.312827

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