In the rodent uterus, the metrial gland develops during midpregnancy a
nd undergoes regression prior to parturation. The involution of the gl
and is reported to be accompanied by the loss of gland cells due to th
eir death in situ. Cell death has been classified by using morphologic
al criteria into two types: necrosis and apoptosis. To study the mecha
nism involved in the peripartum regression of the rat metrial gland, w
e examined the mode of cell death in the gland during the last week of
gestation. We identified apoptotic cells in the regressing metrial gl
and by using DNA fragmentation, in situ DNA 3'-end labeling, and elect
ron microscopy. Expression of progesterone receptor (PR) and estrogen
receptor (ER) was also demonstrated by immunohistochemistry in the gla
nd. The mean weight of metrial gland nodes decreased after day 18 of p
regnancy. The apoptotic granulated metrial gland (GMG) cells that were
detected by using the in situ DNA 3'-end labeling method were observe
d on day 16 of pregnancy, and they increased in number after day 20 of
pregnancy. Intense fragmentation of DNA was also found from day 20 to
day 22 of pregnancy. Electron microscopy demonstrated apoptotic GMG c
ells in the regressing metrial glands, confirming the results of the l
abeling studies. Immunohistochemical study revealed that expression of
PR and ER, which were localized mainly in fibroblast-like stromal cel
ls but not in GMG cells, was almost unchanged during late pregnancy. A
poptotic cell death is the major mode of rat metrial gland cell death
in the peripartum loss of metrial gland cells. Anat. Rec. 252:369-377,
1998. (C) 1998 Wiley-Liss, Inc.