DNA-DAMAGE AND REPAIR IN RABBIT LENS EPITHELIAL-CELLS FOLLOWING UVA RADIATION

Since ultraviolet light may be a contributing factor to cataractogenes is, we investigated the response of the lens epithelium, a potential t arget for UV insult, to UVA radiation. Cell survival and the induction and repair of DNA single-strand breaks (SSBs) were measured in cultur ed rabbit lens epithelial cells following UVA exposure. The light was passed through a filter which eliminated wavelengths below 335 nm in o rder to ensure that the cells were exposed only to UVA. In order to st udy the effect of various fluences of UVA on cell survival, 2 x 10(6) cells suspended in Tyrode's buffer were exposed to UVA. During all irr adiations the cells were maintained at 0.5-degrees-C in order to minim ize DNA repair. Following UVA treatment, 200 cells were cultured in mi nimal essential medium containing 10% rabbit serum, and a colony formi ng assay was used to quantify cell survival. UVA induced cell death in a dose-dependent manner. In additional experiments, confluent epithel ial cells on glass slides immersed in Tyrode's buffer were irradiated and SSBs were quantified using the alkaline elution technique. A 30 mi n exposure to UVA (180 KJ/m2) induced measurable SSBs. An increase in UVA fluence brought about an increase in the number of DNA SSBs. Rejoi ning of SSBs was measured after the cells were irradiated in Tyrode's for 2 hrs and allowed to repair in the dark for 4 hrs at 36-degrees-C in MEM containing 10% serum. Eighty percent of the DNA SSBs were repai red within 4 hrs as determined by analysis of the alkaline elution pro file. The repair kinetics were biphasic with an initial fast and subse quently slower component. The results indicate that UVA can induce SSB s in lens epithelial cells, that the cells can repair most UVA-induced SSBs, and that UVA treatment can be toxic to the epithelium.