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Non-telecentric two-photon microscopy for 3D random access mesoscale imaging

Diffraction-limited two-photon microscopy permits minimally invasive optical monitoring of neuronal activity. However, most conventional two-photon microscopes impose significant constraints on the size of the imaging field-of-view and the specific shape of the effective excitation volume, thus limi...

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Autores principales: Janiak, F. K., Bartel, P., Bale, M. R., Yoshimatsu, T., Komulainen, E., Zhou, M., Staras, K., Prieto-Godino, L. L., Euler, T., Maravall, M., Baden, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795402/
https://www.ncbi.nlm.nih.gov/pubmed/35087041
http://dx.doi.org/10.1038/s41467-022-28192-0
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author Janiak, F. K.
Bartel, P.
Bale, M. R.
Yoshimatsu, T.
Komulainen, E.
Zhou, M.
Staras, K.
Prieto-Godino, L. L.
Euler, T.
Maravall, M.
Baden, T.
author_facet Janiak, F. K.
Bartel, P.
Bale, M. R.
Yoshimatsu, T.
Komulainen, E.
Zhou, M.
Staras, K.
Prieto-Godino, L. L.
Euler, T.
Maravall, M.
Baden, T.
author_sort Janiak, F. K.
collection PubMed
description Diffraction-limited two-photon microscopy permits minimally invasive optical monitoring of neuronal activity. However, most conventional two-photon microscopes impose significant constraints on the size of the imaging field-of-view and the specific shape of the effective excitation volume, thus limiting the scope of biological questions that can be addressed and the information obtainable. Here, employing a non-telecentric optical design, we present a low-cost, easily implemented and flexible solution to address these limitations, offering a several-fold expanded three-dimensional field of view. Moreover, rapid laser-focus control via an electrically tunable lens allows near-simultaneous imaging of remote regions separated in three dimensions and permits the bending of imaging planes to follow natural curvatures in biological structures. Crucially, our core design is readily implemented (and reversed) within a matter of hours, making it highly suitable as a base platform for further development. We demonstrate the application of our system for imaging neuronal activity in a variety of examples in zebrafish, mice and fruit flies.
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spelling pubmed-87954022022-02-07 Non-telecentric two-photon microscopy for 3D random access mesoscale imaging Janiak, F. K. Bartel, P. Bale, M. R. Yoshimatsu, T. Komulainen, E. Zhou, M. Staras, K. Prieto-Godino, L. L. Euler, T. Maravall, M. Baden, T. Nat Commun Article Diffraction-limited two-photon microscopy permits minimally invasive optical monitoring of neuronal activity. However, most conventional two-photon microscopes impose significant constraints on the size of the imaging field-of-view and the specific shape of the effective excitation volume, thus limiting the scope of biological questions that can be addressed and the information obtainable. Here, employing a non-telecentric optical design, we present a low-cost, easily implemented and flexible solution to address these limitations, offering a several-fold expanded three-dimensional field of view. Moreover, rapid laser-focus control via an electrically tunable lens allows near-simultaneous imaging of remote regions separated in three dimensions and permits the bending of imaging planes to follow natural curvatures in biological structures. Crucially, our core design is readily implemented (and reversed) within a matter of hours, making it highly suitable as a base platform for further development. We demonstrate the application of our system for imaging neuronal activity in a variety of examples in zebrafish, mice and fruit flies. Nature Publishing Group UK 2022-01-27 /pmc/articles/PMC8795402/ /pubmed/35087041 http://dx.doi.org/10.1038/s41467-022-28192-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Janiak, F. K.
Bartel, P.
Bale, M. R.
Yoshimatsu, T.
Komulainen, E.
Zhou, M.
Staras, K.
Prieto-Godino, L. L.
Euler, T.
Maravall, M.
Baden, T.
Non-telecentric two-photon microscopy for 3D random access mesoscale imaging
title Non-telecentric two-photon microscopy for 3D random access mesoscale imaging
title_full Non-telecentric two-photon microscopy for 3D random access mesoscale imaging
title_fullStr Non-telecentric two-photon microscopy for 3D random access mesoscale imaging
title_full_unstemmed Non-telecentric two-photon microscopy for 3D random access mesoscale imaging
title_short Non-telecentric two-photon microscopy for 3D random access mesoscale imaging
title_sort non-telecentric two-photon microscopy for 3d random access mesoscale imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795402/
https://www.ncbi.nlm.nih.gov/pubmed/35087041
http://dx.doi.org/10.1038/s41467-022-28192-0
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