Share Email Print

Journal of Biomedical Optics

Pulsed-laser-induced damage in rat corneas: time-resolved imaging of physical effects and acute biological response
Format Member Price Non-Member Price
PDF $20.00 $25.00
cover GOOD NEWS! Your organization subscribes to the SPIE Digital Library. You may be able to download this paper for free. Check Access

Paper Abstract

Laser-induced damage is studied in the rat corneal epithelium and stroma using a combination of time-resolved imaging and biological assays. Cavitation bubble interactions with cells are visualized at a higher spatial resolution than previously reported. The shock wave is observed to propagate through the epithelium without cell displacement or deformation. Cavitation bubble expansion is damped in tissue with a reduction in maximum size in the range of 54 to 59%, as compared to 2-D and 3-D cultures. Bubble expansion on nanosecond timescales results in rupture of the epithelial sheet and severe compression of cell layers beyond the bubble rim. In the stroma, the dense collagen lamellae strongly damped bubble expansion, thus resulting in reduced damage. The acute biological response of this tissue to laser pulses is characterized by confocal fluorescence microscopy. A viability assay of the epithelium reveals that only cells around the immediate site of laser focus are killed, while cells seen to undergo large deformations remain alive. Actin morphology in cells facing this mechanical stress is unchanged. Collagen microstructure in the stroma as revealed by second-harmonic imaging around the ablation site shows minimal disruption. These cellular responses are also compared to in vitro 2-D and 3-D cell cultures.

Paper Details

Date Published: 1 March 2008
PDF: 10 pages
J. Biomed. Opt. 13(2) 024009 doi: 10.1117/1.2907214
Published in: Journal of Biomedical Optics Volume 13, Issue 2
Show Author Affiliations
Anoop V. Cherian, National Ctr. for Biological Sciences (India)
Kaustubh R. Rau, National Ctr. for Biological Sciences (India)

© SPIE. Terms of Use
Back to Top