Exposure of MCF-7 cells to single and/or repeated low gamma -ray doses (0.5
to 8 Gy) resulted in a decrease in the capacity of these cells to concentr
ate tritiated estradiol ([H-3]E-2) (reduction of the number of binding site
s). The decrease in the [H-3]E-2-binding capacity was higher than the survi
val rate, indicating that it could not be ascribed to cell death. Moreover,
such low irradiation doses failed to similarly affect the specific incorpo
ration of [H-3]ORG 2058, even when the progesterone receptor was induced by
E-2, a finding that rejects the hypothesis of a nonspecific effect on all
steroid hormone receptors. This loss of [H-3]E-2 binding was reflected by t
he elimination of the estrogen receptor alpha (ER) when the latter was asse
ssed by immunocytochemistry. However, additional immunochemical studies (We
stern blot data) performed on cell extracts under denaturing conditions fai
led to show any similar elimination of the ER peptide, suggesting that the
loss of E-2-binding capacity would be relevant to subtle changes in the ER
structure and/or ER-associated proteins. The loss of binding capacity, prod
uced by a 3-Gy irradiation, failed to decrease the sensitivity of the cells
to E-2, since progesterone receptor induction and growth stimulation were
maintained. Insufficient ER diminution may explain this observation. (C) 20
01 Wiley-Liss, Inc.