One of the fundamental processes by which hormone action is regulated is by preventing the interaction of the hormone-receptor complex with the effector system. This phenomenon, typically referred to as """"""""desensitization"""""""" has a rapid onset and occurs without changes in the number of hormone receptors. The studies proposed in this application take advantage of the knowledge and reagents gained by the recent cloning and functional expression of a cDNA encoding for the rat follitropin (FSH) receptor to elucidate the molecular basis of the desensitization of FSH responses. We will establish and characterize a simple experimental system to study the desensitization of FSH responses and we will use this system to identify and characterize potential modifications of the FSH receptor that may be involved in the process of desensitization. Once a given receptor modification is identified, its potential importance to the process of desensitization will be documented by functional analysis of FSH receptor mutants prepared by site-directed mutagenesis. Finally, experiments will be initiated to isolate and characterize the enzyme(s) responsible for the receptor modifications. Our knowledge about the molecular basis of the desensitization of FSH responses is rather limited. The proposed studies should help narrow this gap. Since the gonadotropins play central roles in male and female reproduction, imbalances in the circulating levels of these hormones or in the ability of their target cells to respond to then usually has catastrophic effects on reproductive processes. Thus, a complete under- standing of the regulation of gonadotropin actions is a major aspect of the field of reproductive biology.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD028962-02
Application #
3330475
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1992-04-01
Project End
1995-03-31
Budget Start
1993-04-01
Budget End
1994-03-31
Support Year
2
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Andric, Nebojsa; Thomas, Mika; Ascoli, Mario (2010) Transactivation of the epidermal growth factor receptor is involved in the lutropin receptor-mediated down-regulation of ovarian aromatase expression in vivo. Mol Endocrinol 24:552-60
Andric, Nebojsa; Ascoli, Mario (2008) Mutations of the lutropin/choriogonadotropin receptor that do not activate the phosphoinositide cascade allow hCG to induce aromatase expression in immature rat granulosa cells. Mol Cell Endocrinol 285:62-72
Andric, Nebojsa; Ascoli, Mario (2008) The luteinizing hormone receptor-activated extracellularly regulated kinase-1/2 cascade stimulates epiregulin release from granulosa cells. Endocrinology 149:5549-56
Andric, Nebojsa; Ascoli, Mario (2006) A delayed gonadotropin-dependent and growth factor-mediated activation of the extracellular signal-regulated kinase 1/2 cascade negatively regulates aromatase expression in granulosa cells. Mol Endocrinol 20:3308-20
Bhaskaran, R S; Ascoli, M (2005) The post-endocytotic fate of the gonadotropin receptors is an important determinant of the desensitization of gonadotropin responses. J Mol Endocrinol 34:447-57
Donadeu, Francesc Xavier; Ascoli, Mario (2005) The differential effects of the gonadotropin receptors on aromatase expression in primary cultures of immature rat granulosa cells are highly dependent on the density of receptors expressed and the activation of the inositol phosphate cascade. Endocrinology 146:3907-16
Krishnamurthy, Hanumanthappa; Kishi, Hiroshi; Shi, Mei et al. (2003) Postendocytotic trafficking of the follicle-stimulating hormone (FSH)-FSH receptor complex. Mol Endocrinol 17:2162-76
Bhaskaran, Ravi Sankar; Min, Le; Krishnamurthy, Hanumanthappa et al. (2003) Studies with chimeras of the gonadotropin receptors reveal the importance of third intracellular loop threonines on the formation of the receptor/nonvisual arrestin complex. Biochemistry 42:13950-9
Krishnamurthy, Hanumanthappa; Galet, Colette; Ascoli, Mario (2003) The association of arrestin-3 with the follitropin receptor depends on receptor activation and phosphorylation. Mol Cell Endocrinol 204:127-40
Kishi, Hiroshi; Krishnamurthy, Hanumanthappa; Galet, Colette et al. (2002) Identification of a short linear sequence present in the C-terminal tail of the rat follitropin receptor that modulates arrestin-3 binding in a phosphorylation-independent fashion. J Biol Chem 277:21939-46

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