Leukemia inhibitory factor produced at the fetomaternal interface stimulates chorionic gonadotropin production: its possible implication during pregnancy, including implantation period

• Published in: The journal of clinical endocrinology and metabolism Vol. 80; no. 4; p. 1449
• Main Authors: Sawai, K, Matsuzaki, N, Kameda, T, Hashimoto, K, Okada, T, Shimoya, K, Nobunaga, T, Taga, T, Kishimoto, T, Saji, F
• Format: Journal Article
• Language: English
• Published: United States 01.04.1995
• Subjects: Antibodies - immunology; Antigens, CD; Chorionic Gonadotropin - biosynthesis; Chorionic Villi - metabolism; Cytokine Receptor gp130; Decidua - metabolism; Embryo Implantation - physiology; Female; Genistein; Growth Inhibitors - pharmacology; Growth Inhibitors - physiology; Humans; Interleukin-6; Isoflavones - pharmacology; Leukemia Inhibitory Factor; Lymphokines - pharmacology; Lymphokines - physiology; Membrane Glycoproteins - metabolism; Placenta - metabolism; Pregnancy - physiology; Protein-Tyrosine Kinases - antagonists & inhibitors; Recombinant Proteins
• ISSN: 0021-972X
• DOI: 10.1210/jc.80.4.1449

We investigated the role of leukemia inhibitory factor (LIF) at the implantation site of human embryos. The first trimester decidual tissue produced higher levels of LIF than chorionic tissue, but the decidua produced much smaller amounts of interleukin-6 (IL-6) than the chorion in vitro, as determined by enzyme-linked immunosorbent assay. The reverse transcription-polymerase chain reaction and immunohistochemical analysis revealed the expression and localization, on the trophoblasts, of glycoprotein 130 (gp130), an IL-6 signal transducer receptor component shared by the cytokines such as LIF and IL-6. Trophoblasts stimulated by recombinant LIF (rLIF) produced CG titer at the amount similar to that induced by rIL-6. Recombinant LIF-induced CG production was significantly blocked by anti-gp130 antibody but not by anti-IL-6 receptor antibody, whereas rIL-6-induced CG was completely blocked by both antibodies. Recombinant LIF- and rIL-6-induced CG productions were both significantly blocked by genistein, a tyrosine kinase inhibitor, suggesting an involvement of tyrosine kinase in gp130-mediated CG production. Since CG is capable of stimulating trophoblast growth and differentiation as well as placental metabolism, LIF produced at the fetomaternal interface are considered to stimulate the trophoblasts to produce CG, which may contribute to the maintenance of the placental functions and embryonal growth.