F. Gaytan et al., MACROPHAGES, CELL-PROLIFERATION, AND CELL-DEATH IN THE HUMAN MENSTRUAL CORPUS-LUTEUM, Biology of reproduction, 59(2), 1998, pp. 417-425
We studied the presence and numbers of macrophages in the different co
mpartments of the human menstrual corpus luteum (CL) in relation to th
e proliferative activity and apoptosis in luteal cells. Macrophages we
re recognized by immunohistochemical demonstration of the lysosome-ass
ociated glycoprotein CD68, and proliferating cells by immunohistochemi
cal detection of the cell cycle-related protein Ki67 and by counting m
itotic cells. In general, changes in the number of macrophages were pa
rallel to the functional activity of the CL. Macrophage numbers increa
sed up to the end of the early luteal phase, remained relatively uncha
nged during the midluteal phase, and decreased at the late luteal phas
e. Furthermore, macrophages showed prominent morphological changes dur
ing the cycle. They showed round or elongated cytoplasm during the ear
ly and late luteal phases, and dendritic features in the midluteal pha
se. Proliferating cells were very abundant on Days 15-16 and showed a
significant decrease thereafter. Most proliferating cells corresponded
to stromal (mainly vascular) cells. However, about 5% of granulosa-lu
tein cells and about 15% of theca-lutein cells were proliferating duri
ng the early and midluteal phases. Regression of the CL at the late lu
teal phase was associated with both a decrease in the number of prolif
erating cells and an increase in the number of apoptotic cells, which
were highly increased on Days 25-27 of the cycle. The number of macrop
hages was not related to cell proliferation nor to cell death during t
he luteal phase. The observed changes in both macrophage number and mo
rphology suggest the existence of a bidirectional communication betwee
n macrophages and steroidogenic cells in the human CL, or regulation o
f both cell populations by similar mechanisms.