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Hard-wired lattice light-sheet microscopy for imaging of expanded samples
被引:4
|作者:
Stockhausen, Anne
[1
]
Buergers, Jana
[1
]
Rodriguez-Gatica, Juan Eduardo
[1
]
Schweihoff, Jens
[2
]
Merkel, Rudolf
[3
]
Prigge, Jens Markus
[4
]
Schwarz, Martin Karl
[2
]
Kubitscheck, Ulrich
[1
]
机构:
[1] Univ Bonn, Inst Phys & Theoret Chem, Wegelerstr 12, D-53115 Bonn, Germany
[2] Univ Bonn Med Sch, Inst Expt Epileptol & Cognit Res EECR, Sigmund Freud Str 25, D-53127 Bonn, Germany
[3] Forschungszentrum Julich, Inst Biol Informat Proc 2 Mechanobiol, D-52425 Julich, Germany
[4] Forschungszentrum Julich, Inst Biol Informat Proc Mech Workshop, D-52425 Julich, Germany
来源:
关键词:
D O I:
10.1364/OE.393728
中图分类号:
O43 [光学];
学科分类号:
070207 ;
0803 ;
摘要:
Light-sheet fluorescence microscopy (LSFM) helps investigate small structures in developing cells and tissue for three-dimensional localization microscopy and large-field brain imaging in neuroscience. Lattice light-sheet microscopy is a recent development with great potential to improve axial resolution and usable field sizes, thus improving imaging speed. In contrast to the commonly employed Gaussian beams for light-sheet generation in conventional LSFM, in lattice light-sheet microscopy an array of low diverging Bessel beams with a suppressed side lobe structure is used. We developed a facile elementary lattice light-sheet microscope using a micro-fabricated fixed ring mask for lattice light-sheet generation. In our setup, optical hardware elements enable a stable and simple illumination path without the need for spatial light modulators. This setup, in combination with long-working distance objectives and the possibility for simultaneous dual-color imaging, provides optimal conditions for imaging extended optically cleared tissue samples. We here present experimental data of fluorescently stained neurons and neurites from mouse hippocampus following tissue expansion and demonstrate the high homogeneous resolution throughout the entire imaged volume. Utilizing our purpose-built lattice light-sheet microscope, we reached a homogeneous excitation and an axial resolution of 1.2 mu m over a field of view of (333 mu m)(2). (c) 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
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页码:15587 / 15600
页数:14
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