Chromosomal defects are frequently present in malignant and premalignant sk
in disorders; however, it is not known whether ultraviolet radiation from s
unlight plays a role in their induction. To obtain information on the abili
ty of ultraviolet A and ultraviolet B to induce chromosomal aberrations, cu
ltured melanocytes and fibroblasts were exposed to physiologic doses of ult
raviolet A or ultraviolet B and, for comparison, to gamma rays. As a measur
e of chromosomal aberrations, the formation of micronuclei was determined.
To obtain sufficient statistical data on induced micronuclei and cell kinet
ics, a flow cytometry method has been modified and applied. The flow cytome
try method analysis is based on staining the DNA with ethidium bromide and
the cell membranes with 1,6-diphenyl-1,3,5,-hexatriene, We observed dose-de
pendent micronuclei formation after gamma or ultraviolet B irradiation in b
oth cell types and also for ultraviolet A in fibroblasts. The yield of micr
onuclei induced in fibroblasts by ultraviolet A was only a factor 15 smalle
r than that induced by ultraviolet B (313 nm). The results indicate that 10
kJ per m(2) (equivalent to 1 minimal erythema dose) of ultraviolet B and 1
50 kJ per m(2) of ultraviolet A (0.2 minimal erythema dose) can induce 1% o
f micronuclei in fibroblasts, equivalent to the induction due to 0.6 Gy of
gamma radiation. In conclusion, physiologic doses of sunlight can induce ch
romosomal aberrations at a level comparable with that observed after exposu
re to approximately 1 Gy of ionizing radiation. Therefore, sunlight can be
considered a potential inducer of chromosomal aberrations in skin cells, wh
ich may contribute to skin carcinogenesis.