In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells

被引:138
作者
Gray, Daniel C.
Merigan, William
Wolfing, Jessica I.
Gee, Bernard P.
Porter, Jason
Dubra, Alfredo
Twietmeyer, Ted H.
Ahmad, Kamran
Tumbar, Remy
Reinholz, Fred
Williams, David R.
机构
[1] Univ Rochester, Ctr Visual Sci, Rochester, NY 14627 USA
[2] Univ Rochester, Inst Opt, Rochester, NY 14627 USA
[3] Univ Rochester, Inst Eye, Rochester, NY 14642 USA
关键词
D O I
10.1364/OE.14.007144
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The ability to resolve single cells noninvasively in the living retina has important applications for the study of normal retina, diseased retina, and the efficacy of therapies for retinal disease. We describe a new instrument for high-resolution, in vivo imaging of the mammalian retina that combines the benefits of confocal detection, adaptive optics, multispectral, and fluorescence imaging. The instrument is capable of imaging single ganglion cells and their axons through retrograde transport in ganglion cells of fluorescent dyes injected into the monkey lateral geniculate nucleus (LGN). In addition, we demonstrate a method involving simultaneous imaging in two spectral bands that allows the integration of very weak signals across many frames despite inter-frame movement of the eye. With this method, we are also able to resolve the smallest retinal capillaries in fluorescein angiography and the mosaic of retinal pigment epithelium (RPE) cells with lipofuscin autofluorescence. (c) 2006 Optical Society of America
引用
收藏
页码:7144 / 7158
页数:15
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