To identify lactoferrin (LF) and determine its estrogen-responsiveness in t
he rat uterus, immature Sprague-Dawley rats were untreated or subcutaneousl
y injected with 17 beta-estradiol (500 mu g/kg) for 3 days and uterine tiss
ues collected. Outbred immature CD-1 mice, treated with 17 beta-estradiol,
provided the positive control. By using a polyclonal antibody raised agains
t mouse LF, minimal detectable protein was immunolocalized in uterine epith
elial cells of untreated immature rats and mice. After estrogen treatment,
LF was localized in all uterine epithelial cells of both species, although
staining was more intense in mice than rats. In mice, LF was evenly distrib
uted throughout the cytoplasm with intense staining in some cells, while in
rats, it was seen mainly in the apical cytoplasm. For comparison to anothe
r well-known estrogen responsive protein in rats, complement C3 was immunol
ocalized within epithelial cells and it showed a different staining pattern
than LF. Uterine tissue homogenates were analyzed by sodium dodecyl sulfat
e-polyacrylamide gel electrophoresis and Western blots showed cross-reactiv
ity with the mouse LF antibody. These findings indicate that LF is present
in the rat uterus, and is induced by estrogens as reported in other species
. Thus, LF is an important marker of estrogenic activity across species and
will, therefore, have utility in screening for effects of environmental es
trogenic compounds. Published by Elsevier Science Inc.