| Literature DB >> 29582592 |
Tschackad Kamali1, Jörg Fischer1, Spring Farrell2,3, William H Baldridge2,4,5, Gerhard Zinser1, Balwantray C Chauhan2,3,5.
Abstract
We have developed a compact hollow core fiber (HCF)-based imaging platform capable of simultaneous in vivo confocal reflectance and two-photon imaging through the mouse pupil. We demonstrate the performance of this platform by imaging retinal ganglion cells (RGCs) in which the fluorophores YFP and GCaMP3 are expressed in Thy1-YFP-16 and Thy1-GCaMP3 transgenic mice, respectively. Confocal reflectance images of the mouse retina served as a reference for the simultaneous acquisition of the two-photon signals that clearly showed RGCs with single-cell resolution. The use of an HCF platform makes the system compact with future application in the longitudinal investigation into the structure and function of healthy and diseased RGCs. (2018) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE).Entities:
Keywords: biomedical optics; fluorescence microscopy; ophthalmic devices; photonics; two-photon microscopy
Mesh:
Year: 2018 PMID: 29582592 DOI: 10.1117/1.JBO.23.9.091405
Source DB: PubMed Journal: J Biomed Opt ISSN: 1083-3668 Impact factor: 3.170