Objective: To determine if apoptosis is involved in development of the
human fetal mullerian tract and regression of the uterine septum and
to localize Bcl-2, a protein involved with regulating apoptosis. Desig
n: Descriptive controlled study. Setting: Tertiary academic medical ce
nter. Patient(s): Eight human fetal uteri from 12 to 21 weeks' gestati
on. Intervention(s): Immunohistochemistry using a monoclonal antibody
for Bcl-2. Main Outcome Measure(s): Immunostaining. Results: Bcl-2 was
localized in endometrial cells, tubal muscularis and epithelium, and
myometrial edges. It was absent from the septum of 4 uteri. Conclusion
s: The presence of Bcl-2 suggests that development of the human fetal
mullerian tract involves apoptosis. Bcl-2 may protect the fetal endome
trium from apoptosis as it continues to grow. The superior, inferior,
and lateral myometrium as well as the tubal epithelium and muscularis
also may represent active growth zones that are protected from apoptos
is. The notable absence of staining for Bcl-2 in the embryonal uterine
septum may indicate lack of protection from apoptosis in this area. T
his finding supports our hypothesis that apoptosis may be a mechanism
by which the uterine septum regresses. (Fertil Steril(R) 1998;70:135-4
0. (C) 1998 by American Society for Reproductive Medicine.).