The mechanisms of luteal regression and rescue in women are unknown bu
t forms of programmed cell death may be involved. The proto-oncogene b
cl-2 is an important inhibitor of apoptosis but has not previously bee
n described in the human corpus luteum. Immunohistochemical localizati
on of bcl-2 protein was investigated in human corpora lutea obtained f
rom women undergoing surgery during endocrine monitored menstrual cycl
es as well as from women who had been treated with human chorionic gon
adotrophin (HCG) to prolong the luteal phase, Bcl-2 was found to be lo
calized in granulosa-lutein, theca-lutein (as identified by co-localiz
ation of P450(17 alpha-hydroxylase)) and the endothelial cells around
some blood vessels. Immunoblotting demonstrated the presence of a sing
le band of similar to MW 26 kDa. There was no apparent change in eithe
r the intensity of immunostaining or the histological localization dur
ing the normal luteal phase or following treatment with human chorioni
c gonadotrophin. The product of the proto-oncogene bcl-2 is present in
the human corpus luteum, It is unlikely that bcl-2 expression alone i
s responsible for prolongation of the lifespan of the corpus luteum in
early pregnancy although it is possible that the action of the bcl-2
gene present is modified by changes in other members of the bcl-2 fami
ly.