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

被引:5
|
作者
May, Molly A. [1 ]
Bawart, Martin [1 ]
Langeslag, Michiel [2 ]
Bernet, Stefan [1 ]
Kress, Michaela [2 ]
Ritsch-Marte, Monika [1 ]
Jesacher, Alexander [1 ]
机构
[1] Med Univ Innsbruck, Inst Biomed Phys, Mullerstr 44, A-6020 Innsbruck, Austria
[2] Med Univ Innsbruck, Inst Physiol, Schopfstr 41, A-6020 Innsbruck, Austria
来源
BIOMEDICAL OPTICS EXPRESS | 2020年 / 11卷 / 12期
基金
奥地利科学基金会;
关键词
CONJUGATE ADAPTIVE OPTICS; ACOUSTOOPTIC LENS; MICROSCOPY;
D O I
10.1364/BOE.405863
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 mu m. Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License.
引用
收藏
页码:7183 / 7191
页数:9
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