Periscope for noninvasive two-photon imaging of murine retina in vivo

被引:19
|
作者
Stremplewski, Patrycjusz [1 ]
Komar, Katarzyna [1 ]
Palczewski, Krzysztof [2 ]
Wojtkowski, Maciej [1 ]
Palczewska, Grazyna [3 ]
机构
[1] Nicholas Copernicus Univ, Fac Phys Astron & Informat, Inst Phys, PL-87100 Torun, Poland
[2] Case Western Reserve Univ, Sch Med, Cleveland Ctr Membrane & Struct Biol, Dept Pharmacol, Cleveland, OH 44106 USA
[3] Polgenix Inc, Dept Med Devices, Cleveland, OH 44106 USA
来源
BIOMEDICAL OPTICS EXPRESS | 2015年 / 6卷 / 09期
基金
美国国家卫生研究院;
关键词
PIGMENT EPITHELIAL-CELLS; MOUSE RETINA; FLUORESCENCE MICROSCOPY; EYE; LASER; MICE;
D O I
10.1364/BOE.6.003352
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Two-photon microscopy allows visualization of subcellular structures in the living animal retina. In previously reported experiments it was necessary to apply a contact lens to each subject. Extending this technology to larger animals would require fitting a custom contact lens to each animal and cumbersome placement of the living animal head on microscope stage. Here we demonstrate a new device, periscope, for coupling light energy into mouse eye and capturing emitted fluorescence. Using this periscope we obtained images of the RPE and their subcellular organelles, retinosomes, with larger field of view than previously reported. This periscope provides an interface with a commercial microscope, does not require contact lens and its design could be modified to image retina in larger animals. (C) 2015 Optical Society of America
引用
收藏
页码:3352 / 3361
页数:10
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