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Adaptive optics retinal imaging in the living mouse eye

Correction of the eye’s monochromatic aberrations using adaptive optics (AO) can improve the resolution of in vivo mouse retinal images [Biss et al., Opt. Lett. 32(6), 659 (2007) and Alt et al., Proc. SPIE 7550, 755019 (2010)], but previous attempts have been limited by poor spot quality in the Shac...

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Autores principales: Geng, Ying, Dubra, Alfredo, Yin, Lu, Merigan, William H., Sharma, Robin, Libby, Richard T., Williams, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3345801/
https://www.ncbi.nlm.nih.gov/pubmed/22574260
http://dx.doi.org/10.1364/BOE.3.000715
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author Geng, Ying
Dubra, Alfredo
Yin, Lu
Merigan, William H.
Sharma, Robin
Libby, Richard T.
Williams, David R.
author_facet Geng, Ying
Dubra, Alfredo
Yin, Lu
Merigan, William H.
Sharma, Robin
Libby, Richard T.
Williams, David R.
author_sort Geng, Ying
collection PubMed
description Correction of the eye’s monochromatic aberrations using adaptive optics (AO) can improve the resolution of in vivo mouse retinal images [Biss et al., Opt. Lett. 32(6), 659 (2007) and Alt et al., Proc. SPIE 7550, 755019 (2010)], but previous attempts have been limited by poor spot quality in the Shack-Hartmann wavefront sensor (SHWS). Recent advances in mouse eye wavefront sensing using an adjustable focus beacon with an annular beam profile have improved the wavefront sensor spot quality [Geng et al., Biomed. Opt. Express 2(4), 717 (2011)], and we have incorporated them into a fluorescence adaptive optics scanning laser ophthalmoscope (AOSLO). The performance of the instrument was tested on the living mouse eye, and images of multiple retinal structures, including the photoreceptor mosaic, nerve fiber bundles, fine capillaries and fluorescently labeled ganglion cells were obtained. The in vivo transverse and axial resolutions of the fluorescence channel of the AOSLO were estimated from the full width half maximum (FWHM) of the line and point spread functions (LSF and PSF), and were found to be better than 0.79 μm ± 0.03 μm (STD)(45% wider than the diffraction limit) and 10.8 μm ± 0.7 μm (STD)(two times the diffraction limit), respectively. The axial positional accuracy was estimated to be 0.36 μm. This resolution and positional accuracy has allowed us to classify many ganglion cell types, such as bistratified ganglion cells, in vivo.
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spelling pubmed-33458012012-05-09 Adaptive optics retinal imaging in the living mouse eye Geng, Ying Dubra, Alfredo Yin, Lu Merigan, William H. Sharma, Robin Libby, Richard T. Williams, David R. Biomed Opt Express Ophthalmology Applications Correction of the eye’s monochromatic aberrations using adaptive optics (AO) can improve the resolution of in vivo mouse retinal images [Biss et al., Opt. Lett. 32(6), 659 (2007) and Alt et al., Proc. SPIE 7550, 755019 (2010)], but previous attempts have been limited by poor spot quality in the Shack-Hartmann wavefront sensor (SHWS). Recent advances in mouse eye wavefront sensing using an adjustable focus beacon with an annular beam profile have improved the wavefront sensor spot quality [Geng et al., Biomed. Opt. Express 2(4), 717 (2011)], and we have incorporated them into a fluorescence adaptive optics scanning laser ophthalmoscope (AOSLO). The performance of the instrument was tested on the living mouse eye, and images of multiple retinal structures, including the photoreceptor mosaic, nerve fiber bundles, fine capillaries and fluorescently labeled ganglion cells were obtained. The in vivo transverse and axial resolutions of the fluorescence channel of the AOSLO were estimated from the full width half maximum (FWHM) of the line and point spread functions (LSF and PSF), and were found to be better than 0.79 μm ± 0.03 μm (STD)(45% wider than the diffraction limit) and 10.8 μm ± 0.7 μm (STD)(two times the diffraction limit), respectively. The axial positional accuracy was estimated to be 0.36 μm. This resolution and positional accuracy has allowed us to classify many ganglion cell types, such as bistratified ganglion cells, in vivo. Optical Society of America 2012-03-15 /pmc/articles/PMC3345801/ /pubmed/22574260 http://dx.doi.org/10.1364/BOE.3.000715 Text en ©2012 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.
spellingShingle Ophthalmology Applications
Geng, Ying
Dubra, Alfredo
Yin, Lu
Merigan, William H.
Sharma, Robin
Libby, Richard T.
Williams, David R.
Adaptive optics retinal imaging in the living mouse eye
title Adaptive optics retinal imaging in the living mouse eye
title_full Adaptive optics retinal imaging in the living mouse eye
title_fullStr Adaptive optics retinal imaging in the living mouse eye
title_full_unstemmed Adaptive optics retinal imaging in the living mouse eye
title_short Adaptive optics retinal imaging in the living mouse eye
title_sort adaptive optics retinal imaging in the living mouse eye
topic Ophthalmology Applications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3345801/
https://www.ncbi.nlm.nih.gov/pubmed/22574260
http://dx.doi.org/10.1364/BOE.3.000715
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