M. Tamura et al., Transforming growth factor-beta isoforms and receptors in endometriotic cysts of the human ovary, AM J REPROD, 42(3), 1999, pp. 160-167
PROBLEM: The present study examined the presence and cellular distribution
of transforming growth factor-beta 1, 2, and 3 isoforms and their type I an
d II receptors in endometriotic cysts of the ovary, relative to their prese
nce in normal endometrial tissue.
METHOD OF STUDY: Thirteen control samples of normal endometrium in the prol
iferative phase and 11 ovarian endometriotic cysts were examined by immunoh
istochemistry for transforming growth factor-beta 1, 2, and 3 isoforms and
their type I and II receptors.
RESULTS: Immunoreactivity for all ligands and receptors was detected in bot
h normal endometrium and endometriotic cysts. Isoform-specific differences
in immunostaining were not detected. Expression of all ligands and receptor
s was significantly increased in epithelial cells of endometriotic cysts co
mpared with those of normal endometrium. On the other hand, stromal cells i
n normal endometrium and endometriotic cysts were only faintly immunostaine
d. Inflammatory cells infiltrating among endometriotic stromal cells contai
ned the highest immunostaining intensity for all ligands and receptors. We
identified nearly all inflammatory cells as macrophages using a specific an
tibody.
CONCLUSIONS: These findings suggest that macrophages in endometriotic tissu
e are a major source of transforming growth factor-beta, which may be an im
portant regulator of cell proliferation in endometriotic cysts through para
crine and autocrine actions.