The establishment and maintenance of pregnancy requires the coordinated activity of a highly specialized maternal tissue: the decidua. Extensive investigation from our laboratory has revealed that one important function of rat decidual cells is their hormone-producing capabilities. We have shown that a defined decidual cell population in the decidua acts as an endocrine gland and secretes hormone related to pituitary and ovarian hormones; decidual PRL-related protein, activin and follistatin. Another defined cell population expresses in abundance alpha2 macroglobulin, a known activin-binding protein and a potent protease inhibitor. The overall objective of our research is to understand the involvement of the decidual cell signaling system in the establishment and maintenance of pregnancy. The focus of this grant is to define the regulation and interactions of these decidua-derived proteins and their role in the maintenance of the right milieu for fetal development. The first specific aim centers on the expression of decidual PRL-related protein and its role both in the decidua and in the corpus luteum. We will express dPRP in insect and bacterial cells and examine the role of this hormone on the production and action of key proteins involved in progesterone metabolism and protein synthesis.
The second aim will focus on the regulation and function of the decidual alpha2 MG gene expression and determine whether alpha2 MG binds to and protects the decidual PRL-related protein from degradation. We will also investigate whether a key role of alpha2 MG is to bind to activin and prevent activin A induced apoptosis. Finally, in the third aim we will test the hypothesis that the decidual cells have an intrinsic ability to secrete activin A and that activin A stimulates the expression of its own gene and induces apoptosis, leading to the regression and reorganization of the decidua which is essential for normal fetal development. We will also test the possibility that during development alpha2 MG and FST, two decidua-derived activin A binding proteins, prevent activin action and direct when and in which cell activin is to be expressed.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD012356-16
Application #
2403072
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1978-12-01
Project End
2001-05-31
Budget Start
1997-06-01
Budget End
1998-05-31
Support Year
16
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Illinois at Chicago
Department
Physiology
Type
Schools of Medicine
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
Le, Jamie A; Wilson, Heather M; Shehu, Aurora et al. (2012) Generation of mice expressing only the long form of the prolactin receptor reveals that both isoforms of the receptor are required for normal ovarian function. Biol Reprod 86:86
Shehu, Aurora; Albarracin, Constance; Devi, Y Sangeeta et al. (2011) The stimulation of HSD17B7 expression by estradiol provides a powerful feed-forward mechanism for estradiol biosynthesis in breast cancer cells. Mol Endocrinol 25:754-66
Le, J A; Wilson, H M; Shehu, A et al. (2011) Prolactin activation of the long form of its cognate receptor causes increased visceral fat and obesity in males as shown in transgenic mice expressing only this receptor subtype. Horm Metab Res 43:931-7
Devi, Y Sangeeta; Seibold, Anita M; Shehu, Aurora et al. (2011) Inhibition of MAPK by prolactin signaling through the short form of its receptor in the ovary and decidua: involvement of a novel phosphatase. J Biol Chem 286:7609-18
Devi, Y Sangeeta; Shehu, Aurora; Halperin, Julia et al. (2009) Prolactin signaling through the short isoform of the mouse prolactin receptor regulates DNA binding of specific transcription factors, often with opposite effects in different reproductive issues. Reprod Biol Endocrinol 7:87
Devi, Y Sangeeta; Shehu, Aurora; Stocco, Carlos et al. (2009) Regulation of transcription factors and repression of Sp1 by prolactin signaling through the short isoform of its cognate receptor. Endocrinology 150:3327-35
Halperin, Julia; Devi, Sangeeta Y; Elizur, Shai et al. (2008) Prolactin signaling through the short form of its receptor represses forkhead transcription factor FOXO3 and its target gene galt causing a severe ovarian defect. Mol Endocrinol 22:513-22
Li, Feixue; Devi, Y Sangeeta; Bao, Lei et al. (2008) Involvement of cyclin D3, CDKN1A (p21), and BIRC5 (Survivin) in interleukin 11 stimulation of decidualization in mice. Biol Reprod 78:127-33
Bao, Lei; Tessier, Christian; Prigent-Tessier, Anne et al. (2007) Decidual prolactin silences the expression of genes detrimental to pregnancy. Endocrinology 148:2326-34
Bao, Lei; Devi, Sangeeta; Bowen-Shauver, Jennifer et al. (2006) The role of interleukin-11 in pregnancy involves up-regulation of alpha2-macroglobulin gene through janus kinase 2-signal transducer and activator of transcription 3 pathway in the decidua. Mol Endocrinol 20:3240-50

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