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Periscope for noninvasive two-photon imaging of murine retina in vivo
Author(s) -
Patrycjusz Stremplewski,
Katarzyna Komar,
Krzysztof Palczewski,
Maciej Wojtkowski,
Grażyna Palczewska
Publication year - 2015
Publication title -
biomedical optics express
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.362
H-Index - 86
ISSN - 2156-7085
DOI - 10.1364/boe.6.003352
Subject(s) - retina , optics , preclinical imaging , two photon excitation microscopy , medical imaging , optical coherence tomography , optical imaging , photon , photon counting , in vivo , physics , computer science , biology , fluorescence , artificial intelligence , microbiology and biotechnology
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.

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