The known accumulation of macrophages in corpora lutea (CL) at the tim
e of luteal regression prompted us to investigate whether the chemoatt
ractant protein monocyte chemoattractant protein-1 (MCP-1) is expresse
d in the rat CL. On the day of confirmed mating (Day 0 of pregnancy),
regressing CL from the previous (nonfertile) estrous cycle contained i
mmunodetectable MCP-1 and numerous monocytes/macrophages, whereas the
newly formed CL of pregnancy, within the same ovary, contained little
MCP-1 and few monocytes/macrophages. MCP-1 diminished in the regressin
g CL on Days 3 and 9 of pregnancy, although numerous monocytes/macroph
ages remained. The CL of pregnancy on Days 3 and 9 of pregnancy contai
ned minimal MCP-1 and relatively few monocytes/macrophages. By Days 17
and 21 of pregnancy, however, prior to parturition and prior to an ac
cumulation of monocytes/macrophages, expression of MCP-1 increased in
the CL of pregnancy. Northern blots revealed a resurgence of luteal MC
P-1 mRNA on Day 21 of pregnancy: 3805 +/- 1077 on Day 21 vs. 1059 +/-
177 on Day 9 (p < 0.05; expressed as densitometric units relative to b
eta-actin). In conclusion, the expression of MCP-1 in the rat CL in as
sociation with, or preceding, the appearance of monocytes/macrophages
at the time of luteal regression is consistent with the known role of
MCP-1 as a potent chemoattractant for monocytes/macrophages. This sugg
ests that MCP-1 might have a prominent role in the immunological proce
ss of luteal regression.