Three-photon fluorescence microscopy with an axially elongated Bessel focus

被引:49
|
作者
Rodriguez, Cristina [1 ]
Liang, Yajie [1 ]
Lu, Rongwen [1 ]
Ji, Na [1 ,2 ]
机构
[1] Howard Hughes Med Inst, Janelia Res Campus, Ashburn, VA 20147 USA
[2] Univ Calif Berkeley, Dept Phys, Dept Mol & Cellular Biol, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
INTACT MOUSE-BRAIN; EXTENDED DEPTH; RESOLUTION; NEURONS; FIELD;
D O I
10.1364/OL.43.001914
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Volumetric imaging tools that are simple to adopt, flexible, and robust are in high demand in the field of neuroscience, where the ability to image neurons and their networks with high spatiotemporal resolution is essential. Using an axially elongated focus approximating a Bessel beam, in combination with two-photon fluorescence microscopy, has proven successful at such an endeavor. Here, we demonstrate three-photon fluorescence imaging with an axially extended Bessel focus. We use an axicon-based module that allowed for the generation of Bessel foci of varying numerical apertures and axial lengths, and apply this volumetric imaging tool to image mouse brain slices and for in vivo imaging of the mouse brain. (C) 2018 Optical Society of America
引用
收藏
页码:1914 / 1917
页数:4
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