| Literature DB >> 19529085 |
Daniel C Gray1, William Merigan, Jessica I Wolfing, Bernard P Gee, Jason Porter, Alfredo Dubra, Ted H Twietmeyer, Kamran Ahamd, Remy Tumbar, Fred Reinholz, David R Williams.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2006 PMID: 19529085 DOI: 10.1364/oe.14.007144
Source DB: PubMed Journal: Opt Express ISSN: 1094-4087 Impact factor: 3.894