We have tested the possibility of using apoptosis (programmed cell dea
th) in human peripheral blood lymphocytes as a short-term biological d
osimeter. Lymphocytes isolated from whole blood were irradiated in cul
ture with 250 kVp x-rays or Co-60 gamma rays, Two assays mere used to
measure apoptosis in lymphocytes after irradiation: ill situ terminal
deoxynucleotidyl transferase assay and fluorescence analysis of DNA un
winding assay, Similar qualitative and quantitative results were produ
ced by the assays, supporting the notion that the fluorescence analysi
s of DNA unwinding assay measured DNA fragmentation associated with ap
optosis. Induction of apoptosis in lymphocytes irradiated in vitro was
proportional to dose and could be detected following exposures as low
as 0.05 Gy, Lymphocytes from individual donors had reproducible dose
responses, There was, however, variation between donors, X-ray and gam
ma-ray exposures induced similar levels of apoptosis at similar doses.
The induction kinetics of apoptosis in vitro indicate a maximum is re
ached about 72 h after irradiation. In conclusion, the in vitro experi
mental evidence indicates that radiation-induced apoptosis in human ly
mphocytes has the kinetics, sensitivity, and reproducibility to be a p
otential biological dosimeter.