Wavefront sensorless adaptive optics fluorescence biomicroscope for in vivo retinal imaging in mice

被引:0
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作者
Wahl, Daniel J. [1 ]
Jian, Yifan [1 ]
Bonora, Stefano [2 ,3 ]
Zawadzki, Robert J. [4 ,5 ]
Sarunic, Marinko V. [1 ]
机构
[1] Engineering Science, Simon Fraser University, Burnaby,BC,V5A 1S6, Canada
[2] CNR-Institute for Photonics and Nanotechnology, Via Trasea 7, Padova,35131, Italy
[3] Institute of Physics AS CR v.v.i, Na Slovance 2, Prague,18221, Czech Republic
[4] UC Davis RISE Small Animal Ocular Imaging Facility, Department of Cell Biology and Human Anatomy, University of California Davis, Davis,CA,95616, United States
[5] Vision Science and Advanced Retinal Imaging Laboratory (VSRI), Department of Ophthalmology and Vision Science, University of California Davis, Sacramento,CA,95817, United States
基金
美国国家科学基金会;
关键词
Proteins - Wavefronts - Mirrors - Ophthalmology - Imaging systems - Mammals - Deformation - Fluorescence imaging;
D O I
10.1364/BOE.7.000001
中图分类号
学科分类号
摘要
Cellular-resolution in vivo fluorescence imaging is a valuable tool for longitudinal studies of retinal function in vision research. Wavefront sensorless adaptive optics (WSAO) is a developing technology that enables high-resolution imaging of the mouse retina. In place of the conventional method of using a Shack-Hartmann wavefront sensor to measure the aberrations directly, WSAO uses an image quality metric and a search algorithm to drive the shape of the adaptive element (i.e. deformable mirror). WSAO is a robust approach to AO and it is compatible with a compact, low-cost lens-based system. In this report, we demonstrated a hill-climbing algorithm for WSAO with a variable focus lens and deformable mirror for non-invasive in vivo imaging of EGFP (enhanced green fluorescent protein) labelled ganglion cells and microglia cells in the mouse retina. ©2015 Optical Society of America.
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