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High-NA two-photon single cell imaging with remote focusing using a diffractive tunable lens

Fast, volumetric structural and functional imaging of cellular and sub-cellular dynamics inside the living brain is one of the most desired capabilities in the neurosciences, but still faces serious challenges. Specifically, while few solutions for rapid 3D scanning exist, it is generally much easie...

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Autores principales: May, Molly A., Bawart, Martin, Langeslag, Michiel, Bernet, Stefan, Kress, Michaela, Ritsch-Marte, Monika, Jesacher, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747902/
https://www.ncbi.nlm.nih.gov/pubmed/33408989
http://dx.doi.org/10.1364/BOE.405863
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author May, Molly A.
Bawart, Martin
Langeslag, Michiel
Bernet, Stefan
Kress, Michaela
Ritsch-Marte, Monika
Jesacher, Alexander
author_facet May, Molly A.
Bawart, Martin
Langeslag, Michiel
Bernet, Stefan
Kress, Michaela
Ritsch-Marte, Monika
Jesacher, Alexander
author_sort May, Molly A.
collection PubMed
description Fast, volumetric structural and functional imaging of cellular and sub-cellular dynamics inside the living brain is one of the most desired capabilities in the neurosciences, but still faces serious challenges. Specifically, while few solutions for rapid 3D scanning exist, it is generally much easier to facilitate fast in-plane scanning than it is to scan axially at high speeds. Remote focusing in which the imaging plane is shifted along the optical axis by a tunable lens while maintaining the position of the sample and objective is a promising approach to increase the axial scan speed, but existing techniques often introduce severe optical aberrations in high-NA imaging systems, eliminating the possibility of diffraction-limited single-cell imaging. Here, we demonstrate near diffraction-limited, volumetric two-photon fluorescence microscopy in which we resolve the deep sub-micron structures of single microglia cells with axial scanning performed using a novel high-NA remote focusing method. Image contrast is maintained to within 7% compared to mechanical sample stepping and the focal volume remains nearly diffraction-limited over an axial range greater than 86 µm.
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spelling pubmed-77479022021-01-05 High-NA two-photon single cell imaging with remote focusing using a diffractive tunable lens May, Molly A. Bawart, Martin Langeslag, Michiel Bernet, Stefan Kress, Michaela Ritsch-Marte, Monika Jesacher, Alexander Biomed Opt Express Article Fast, volumetric structural and functional imaging of cellular and sub-cellular dynamics inside the living brain is one of the most desired capabilities in the neurosciences, but still faces serious challenges. Specifically, while few solutions for rapid 3D scanning exist, it is generally much easier to facilitate fast in-plane scanning than it is to scan axially at high speeds. Remote focusing in which the imaging plane is shifted along the optical axis by a tunable lens while maintaining the position of the sample and objective is a promising approach to increase the axial scan speed, but existing techniques often introduce severe optical aberrations in high-NA imaging systems, eliminating the possibility of diffraction-limited single-cell imaging. Here, we demonstrate near diffraction-limited, volumetric two-photon fluorescence microscopy in which we resolve the deep sub-micron structures of single microglia cells with axial scanning performed using a novel high-NA remote focusing method. Image contrast is maintained to within 7% compared to mechanical sample stepping and the focal volume remains nearly diffraction-limited over an axial range greater than 86 µm. Optical Society of America 2020-11-16 /pmc/articles/PMC7747902/ /pubmed/33408989 http://dx.doi.org/10.1364/BOE.405863 Text en Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI. Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) . Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI.
spellingShingle Article
May, Molly A.
Bawart, Martin
Langeslag, Michiel
Bernet, Stefan
Kress, Michaela
Ritsch-Marte, Monika
Jesacher, Alexander
High-NA two-photon single cell imaging with remote focusing using a diffractive tunable lens
title High-NA two-photon single cell imaging with remote focusing using a diffractive tunable lens
title_full High-NA two-photon single cell imaging with remote focusing using a diffractive tunable lens
title_fullStr High-NA two-photon single cell imaging with remote focusing using a diffractive tunable lens
title_full_unstemmed High-NA two-photon single cell imaging with remote focusing using a diffractive tunable lens
title_short High-NA two-photon single cell imaging with remote focusing using a diffractive tunable lens
title_sort high-na two-photon single cell imaging with remote focusing using a diffractive tunable lens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747902/
https://www.ncbi.nlm.nih.gov/pubmed/33408989
http://dx.doi.org/10.1364/BOE.405863
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