Apoptotic DNA fragmentation was observed 60 min after photodynamic the
rapy of murine leukemia cells in culture, using either of two photosen
sitizers with predominantly lysosomal targets. When the radical scaven
gers trolox or alpha-tocopherol succinate were present during irradiat
ion, the subsequent appearance of apoptotic cells was prevented, as wa
s phototoxicity. Addition of either scavenger during the 60 min after
irradiation provided only partial protection from apoptosis and photot
oxicity; this protection was abolished if the addition was delayed for
10 min. These results are consistent with a model whereby long-persis
ting photoproducts continue the initiation of apoptosis for approximat
ely 10 min after irradiation has ceased.