The mouse placenta produces two placental lactogens: mouse placental lactogen-I (mPL-I) and mPL-II. The long-term objectives of the project are to understand what functions these hormones perform in various target tissues and to understand what regulates their production and concentrations in the fetal and maternal blood. Although relatively little is known at present about the biological activities and regulation of secretion of PLs in various species, it is clear from what is known, that PLs participate in several important processes during pregnancy, such as stimulating mammary gland differentiation, regulating maternal and fetal intermediary metabolism, and stimulating fetal growth. In the long term, investigating the physiology of PLs will contribute to a better understanding of the processes that influence fetal health and survival during pregnancy. The studies outlined in this renewal application are a continuation of previous work in this laboratory on the biological activity and regulation of secretion of mPL-I and mPL-II. A primary culture system will be developed for examining the regulation of mPL-I secretion. It will be used to screen mPL-I secretagogues. The biological activity of mPL-I will be examined with respect to its ability to inhibit prolactin surges in midpregnant mice, using recombinant mPL-I. The regulation of secretion of mPL-II will be examined in several series of experiments. The mechanism by which the pituitary gland suppresses the maternal serum mPL-II concentration will be investigated. A mPL-II-releasing factor present in the decidua will be purified and its physiology will be examined. Effects of gonadotropin-releasing hormone and growth hormone-releasing hormone on the synthesis and release of mPL-II and total placental proteins will be examined and the presence of these peptides in the mouse placenta will be investigated. The biological activity of mPL-II in the maternal mammary gland will be examined with respect to the stimulation of alpha- lactalbumin production. experiments will also be performed to identify proteins whose synthesis is stimulated by mPL-II in fetal mouse hepatocytes.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37HD014966-13
Application #
3485082
Study Section
Reproductive Endocrinology Study Section (REN)
Project Start
1980-12-01
Project End
1993-11-30
Budget Start
1992-12-01
Budget End
1993-11-30
Support Year
13
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of California Santa Cruz
Department
Type
Schools of Arts and Sciences
DUNS #
City
Santa Cruz
State
CA
Country
United States
Zip Code
95064
Talamantes, F; Ortiz, R (2002) Structure and regulation of expression of the mouse GH receptor. J Endocrinol 175:55-9
Shyamala, G; Louie, S G; Camarillo, I G et al. (1999) The progesterone receptor and its isoforms in mammary development. Mol Genet Metab 68:182-90
Contreras, B; Talamantes, F (1999) Growth hormone (GH) and 17beta-estradiol regulation of the expression of mouse GH receptor and GH-binding protein in cultured mouse hepatocytes. Endocrinology 140:4725-31
Moffat, J G; Edens, A; Talamantes, F (1999) Structure and expression of the mouse growth hormone receptor/growth hormone binding protein gene. J Mol Endocrinol 23:33-44
Ilkbahar, Y N; Southard, J N; Talamantes, F (1999) Transcriptional upregulation of hepatic GH receptor and GH-binding protein expression during pregnancy in the mouse. J Mol Endocrinol 23:85-96
Farnsworth, R L; Talamantes, F (1998) Calcyclin in the mouse decidua: expression and effects on placental lactogen secretion. Biol Reprod 59:546-52
Galosy, S S; Talamantes, F (1995) Luteotropic actions of placental lactogens at midpregnancy in the mouse. Endocrinology 136:3993-4003
Southard, J N; Barrett, B A; Bikbulatova, L et al. (1995) Growth hormone (GH) receptor and GH-binding protein messenger ribonucleic acids with alternative 5'-untranslated regions are differentially expressed in mouse liver and placenta. Endocrinology 136:2913-21
Yamaguchi, M; Ogren, L; Kurachi, H et al. (1995) Opposite effects of transforming growth factor alpha and epidermal growth factor on mouse placental lactogen I secretion. Proc Natl Acad Sci U S A 92:2830-4
Ilkbahar, Y N; Wu, K; Thordarson, G et al. (1995) Expression and distribution of messenger ribonucleic acids for growth hormone (GH) receptor and GH-binding protein in mice during pregnancy. Endocrinology 136:386-92

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