Characterization of an Insulin-Like Growth Factor Binding Protein, Analogous to Human Pregnancy-Associated Secreted Endometrial α1-Globulin, in Decidua of the Baboon (Paplo Anubis) Placenta1

Publisher Website
Google Scholar
Abstract
The major secreted protein of the human decidua (pregnancy-associated endometrial .alpha.1-globulin [.alpha.1-PEG]), is an insulin-like growth factor-binding protein (IGF-BP) that is immunologically and biochemically similar to placental protein 12 (PP12) extracted from term human placenta. Since previous studies have demonstrated that the baboon and human endometrium synthesize and release a number of biochemically and immunologically related polypeptides in culture, this study was undertaken to further characterize a related IGF-BP in baboon placental tissues. Decidua, chorio-amniotic membranes with adhering decidua (CAM-D), and placental villi were obtained from pregnancy baboons between Days 134 and 160 of gestation by Cesarean sections. Portions of tissue were either cultured in the presence of 33S-methionine, fixed for immunocytochemistry, or frozen in liquid nitrogen for cytosol extraction. Two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) of tissue culture media (TCM) revealed that the major secretory product of the decidua and CAM-D was an acidic polypeptide (Mr 33,000). Western blot analysis and immunoprecipitation of TCM with murine monoclonal antibody (B2H10) against human .alpha.1-PEG demonstrated that this molecule, secreted by the baboon decidua and CAM-D, but not the placental villi, was immunologically indentical to the human IGF-BP. Immunocytochemical localization of IGF-BP was intense in the cytoplasm of stromal cells in decidua and CAM-D and absent in the placenta. Gel filtration of TCM and cytsol followed by screening of eluates for 125I-IGF-I binding resolved two peaks (Mr > 100,000 and 35,000) of specific IGF-BP in decidua and CAM-D. The 35,00 peak had 100-200 times the binding capacity of the Mr > 100,000 peak and a Kd of 1.14-1.83nM. The eluates contained in the Mr 35,000 peak were also immunoreactive to .alpha.1-PEG, as accessed by a polyclonal radioimmunoassay. Affinity cross-linking with 125I-IGF-I followed by sodium dodecyl sulfate-PAGE revealed an immunoreactive complex of Mr 36,000, confirming that the baboon protein represents a high affinity IGF-BP. These studies indicate that the hypertrophied stromal cells of the baboon decidua and CAM-D synthesize and release an IGF-BP as their major secretory product, analogous to the situation in humans. The results of this study suggest that this protein may play a role in the regulation of IGF action during pregnancy.

This publication has 21 references indexed in Scilit: