Objective-Preterm delivery is often associated with increased cytokine and chemokine production. These studies sought to characterize the expression of the chemokine, monocyte chemotactic protein-1 (MCP-1), in mice during lipopolysaccharide (LPS)-induced preterm delivery.Methods-Uterine and other tissues were harvested from CD-1 mice on gestational day 15 after intrauterine LPS injection. Quantitative real-time reverse-transcriptase polymerase chain reactions (qRT-PCR) determined MCP-1 and toll-like receptor 4 (TLR4) mRNA expression during the 24 hours after LPS. MCP-1 protein expression was determined using a cytokine/chemokine protein array, by ELISA and by immunohistochemistry.Results-Intrauterine LPS injection caused preterm delivery in CD-1 mice between 12 and 24 hours. Expression of MCP-1 mRNA significantly increased at 2 and 6 hours, while TLR4 expression did not significantly change over 24 hours. MCP-1 protein levels peaked by 2 to 6 hours in maternal serum, liver, lung, kidney and uterus. Immunohistochemistry confirmed MCP-1 in myometrium and endometrium.Discussion-These studies have provided evidence suggesting that MCP-1 potentially plays an important role during the proinflammatory immune response leading to preterm labor in the mouse.