Assessment of ocular irritation by image processed quantification of cell injury in human corneal cell cultures and in corneal constructs
By Engelke, M. - Patzke, J. - Tykhonova, S. - Zorn-Kruppa, M.
| Record number: | 2928570 |
|---|---|
| Category: | eye irritation - cornea - cell lines - animal use replacement - endpoints - cell death - image analysis - cytotoxicity |
Currently, there are no accepted alternative tests for the replacement of animals in ocular irritation testing. This study focused on the quantification of cellular viability as a measure of toxic events in immortalised human corneal cell cultures and a three-dimensional corneal construct. Simultaneous vital dye staining by calcein AM and ethidium homodimer-1 was used to provide "live" and "dead" probes, respectively. For further quantification, we have developed image processing tools to evaluate digital images obtained from confocal fluorescence scanning microscopy measurements. Based on the finding that ocular irritation can be related to the extent of cell injury at the various cell layers of the cornea, we extended our studies from corneal cell cultures to an in vitro human corneal equivalent system comprising epithelial, stromal keratocyte and endothelial layers. Our results showed that the microscopic measurement of cellular injury by using either cell cultures or in vitro corneal constructs, combined with image processed quantification, can provide insight into the extent of the toxic effects.
Issued: Oct. 2004
Journal Title: Alternatives to laboratory animals
ISSN: 0261-1929
Volume issue: 32 v. 4 no.
Pages: 345 - 353
Notes:
Paper presented at the "21st Workshop on In Vitro Toxicology" of the Scandinavian Society for Cell Toxicology, September 19-21, 2003, Tampere, Finland.
AGRICOLA identifier: IND43668641
Takk for din tilbakemelding! Vær oppmerksom på at vi ikke kan kontakte deg hvis ikke du oppgir din epostadresse.
Hva lette du etter?
Gi oss gjerne en tilbakemelding slik at vi kan forbedre informasjonen på siden. På forhånd takk for hjelpen! Vennligst skriv inn din epostadresse hvis du vil ha et svar.
Kontakt oss gjerne på e-post hvis du har spørsmål.