EFFECT OF MITOMYCIN-C ON HUMAN RETINAL-PIGMENT EPITHELIUM IN CULTURE

Citation
Tc. Ho et al., EFFECT OF MITOMYCIN-C ON HUMAN RETINAL-PIGMENT EPITHELIUM IN CULTURE, Current eye research, 16(6), 1997, pp. 572-576
Citations number
17
Categorie Soggetti
Ophthalmology
Journal title
ISSN journal
02713683
Volume
16
Issue
6
Year of publication
1997
Pages
572 - 576
Database
ISI
SICI code
0271-3683(1997)16:6<572:EOMOHR>2.0.ZU;2-Z
Abstract
Purpose. To determine the effect of mitomycin-C on confluent and non-c onfluent human retinal pigment epithelium (RPE) in tissue culture. Met hods. The effect of mitomycin-C on confluent RPE was determined by tre ating first passage confluent cells with 0.01, 0.1, 1, 10, 100 or 1000 micromolar (mu M) mitomycin-C for 1, 3. or 7 days. The cell viablilit y after treatment was determined by using an esterase stain. The effec t of mitomycin-C on proliferating RPE was determined by incubating non -confluent cells with the above concentrations of mitomycin-C for 20 m in, 1 hour or 24 hours. Results. Mitomycin-C can be toxic to a conflue nt RPE monolayer, and the LD50 is 421, 28.8 or 0.0632 mu M when cells are continually exposed to mitomycin-C for 1, 3 or 7 days, respectivel y. Exposure to mitomycin-C at concentrations greater than or equal to 10 mu M for 20-60 min significantly inhibits proliferation of non-conf luent RPE. A 24 hour exposure of RPE to 1 mu M mitomycin-C markedly in hibits proliferation of non-confluent RPE with minimal toxicity to con fluent RPE. Conclusions. Since exposure of human RPE to mitomycin-C fo r 24 hours can inhibit cell proliferation at concentrations which are well-tolerated by confluent RPE, mitomycin-C may be a suitable agent f or inhibiting RPE proliferation in vivo.