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Autori principali: Robert, Hadrien L. M., Faini, Giulia, Liu, Chang F., Rutz, Nadja, Aggoun, Anis, Putti, Elena, Garcia-Guirado, Jose, Del Bene, Filippo, Quidant, Romain, Tessier, Gilles, Berto, Pascal
Natura: Preprint
Pubblicazione: 2025
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Accesso online:https://arxiv.org/abs/2501.03965
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author Robert, Hadrien L. M.
Faini, Giulia
Liu, Chang F.
Rutz, Nadja
Aggoun, Anis
Putti, Elena
Garcia-Guirado, Jose
Del Bene, Filippo
Quidant, Romain
Tessier, Gilles
Berto, Pascal
author_facet Robert, Hadrien L. M.
Faini, Giulia
Liu, Chang F.
Rutz, Nadja
Aggoun, Anis
Putti, Elena
Garcia-Guirado, Jose
Del Bene, Filippo
Quidant, Romain
Tessier, Gilles
Berto, Pascal
contents Fluorescence microscopes can record the dynamics of living cells with high spatio-temporal resolution in a single plane. However, monitoring rapid and dim fluorescence fluctuations, e.g induced by neuronal activity in the brain, remains challenging for 3D-distributed emitters due to out-of-focus fluorescence background, a restricted photon budget, and the speed limit of conventional scanning systems. Here, we introduce a Thermally Adaptive Surface strategy, capable of simultaneously recording, at camera framerate, the activity of 3D-distributed objects. This innovative microscope leverages on an array of thermally tuneable microlenses that offer low chromatic aberration and high transmission, and can be combined with patterned illumination to provide optical sectioning. We demonstrate its potential in vivo, by simultaneously monitoring fast fluorescent dynamics at different depths in the zebrafish larval brain, at a rate of 0.5 kHz and over a large field of view (360um x 360um).
format Preprint
id arxiv_https___arxiv_org_abs_2501_03965
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Thermally Adaptive Surface Microscopy for brain functional imaging
Robert, Hadrien L. M.
Faini, Giulia
Liu, Chang F.
Rutz, Nadja
Aggoun, Anis
Putti, Elena
Garcia-Guirado, Jose
Del Bene, Filippo
Quidant, Romain
Tessier, Gilles
Berto, Pascal
Optics
Fluorescence microscopes can record the dynamics of living cells with high spatio-temporal resolution in a single plane. However, monitoring rapid and dim fluorescence fluctuations, e.g induced by neuronal activity in the brain, remains challenging for 3D-distributed emitters due to out-of-focus fluorescence background, a restricted photon budget, and the speed limit of conventional scanning systems. Here, we introduce a Thermally Adaptive Surface strategy, capable of simultaneously recording, at camera framerate, the activity of 3D-distributed objects. This innovative microscope leverages on an array of thermally tuneable microlenses that offer low chromatic aberration and high transmission, and can be combined with patterned illumination to provide optical sectioning. We demonstrate its potential in vivo, by simultaneously monitoring fast fluorescent dynamics at different depths in the zebrafish larval brain, at a rate of 0.5 kHz and over a large field of view (360um x 360um).
title Thermally Adaptive Surface Microscopy for brain functional imaging
topic Optics
url https://arxiv.org/abs/2501.03965