The overall goal of the proposed studies is to determine the molecular mechanism involved in the transformation of normal theca-interstitital cells into androgen hypersecreting cells and the subsequent impairment of the growth and development of ovarian follicles resulting in anovulation. Ovarian hyperandrogenism has been recognized as a major causative factor for anovulation. Although not present in all hyperandrogenic anovulatory conditions, a subset of patients with anovulation has been shown to be insulin resistant with a resultant increase in insulin levels. These conditions are associated with theca-cell hyperplasia, hyperandrogenism and anovulation.
Aim 1 of the proposed studies will examine the molecular basis for insulin and LH action in stimulating theca-interstitial cell androgen production.
This aim will be accomplished by examining the mechanisms involved in the cholesterol transport system via induction of plasma lipoprotein receptors. More specifically, it is proposed to examine the involvement of the transcription factor, Sterol Response Element Binding Protein which regulates the expression of cholesterol responsive genes in the theca-interstitial cells in response to LH and insulin.
In Aim 2, theca-interstitial cell hyperplasia will be examined by determining the regulation of cell cycle at the G1/S interphase by insulin alone or in the presence of LH.
Aim 3 will examine the inhibitory effect of androgens on ovarian follicular growth involving mTOR. This will be accomplished by identifying the signalling pathways involved in the action of mTOR-mediated regulation of granulosa cell growth and development in response to FSH and insulin. The specific step(s) in this pathway affected by dihydrotestosterone will also be determined. It is expected that the studies proposed in this application will help delineate the molecular basis for the secretion of excess androgens by the theca-interstitial cells and the destructive effect these androgens produce in preparing the ovarian follicles for ovulation. The results will have direct bearing on the understanding of the pathophysiology of androgen excess disorders like polycystic ovarian syndrome. Since polycystic ovarian syndrome is one of the most common causes of infertility in women, the proposed study is expected to generate valuable information that may have relevance in the understanding of this complex disorder. ? ? ?

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD038424-08
Application #
7446615
Study Section
Integrative and Clinical Endocrinology and Reproduction Study Section (ICER)
Program Officer
Yoshinaga, Koji
Project Start
1999-12-01
Project End
2011-06-30
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
8
Fiscal Year
2008
Total Cost
$299,718
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Obstetrics & Gynecology
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Palaniappan, Murugesan; Menon, Bindu; Menon, K M J (2013) Stimulatory effect of insulin on theca-interstitial cell proliferation and cell cycle regulatory proteins through MTORC1 dependent pathway. Mol Cell Endocrinol 366:81-9
Palaniappan, Murugesan; Menon, K M J (2012) Luteinizing hormone/human chorionic gonadotropin-mediated activation of mTORC1 signaling is required for androgen synthesis by theca-interstitial cells. Mol Endocrinol 26:1732-42
Kayampilly, Pradeep P; Menon, K M J (2012) AMPK activation by dihydrotestosterone reduces FSH-stimulated cell proliferation in rat granulosa cells by inhibiting ERK signaling pathway. Endocrinology 153:2831-8
Will, Matthew A; Palaniappan, Murugesan; Peegel, Helle et al. (2012) Metformin: direct inhibition of rat ovarian theca-interstitial cell proliferation. Fertil Steril 98:207-14
Palaniappan, Murugesan; Menon, K M J (2010) Human chorionic gonadotropin stimulates theca-interstitial cell proliferation and cell cycle regulatory proteins by a cAMP-dependent activation of AKT/mTORC1 signaling pathway. Mol Endocrinol 24:1782-93
Kayampilly, Pradeep P; Wanamaker, Brett L; Stewart, James A et al. (2010) Stimulatory effect of insulin on 5alpha-reductase type 1 (SRD5A1) expression through an Akt-dependent pathway in ovarian granulosa cells. Endocrinology 151:5030-7
Fisseha, Senait; Towns, Roberto; Harada, Miyuki et al. (2010) Inhibitory effect of valproic acid on ovarian androgen biosynthesis in rat theca-interstitial cells. Endocrine 37:187-93
Kayampilly, Pradeep P; Menon, K M J (2009) Follicle-stimulating hormone inhibits adenosine 5'-monophosphate-activated protein kinase activation and promotes cell proliferation of primary granulosa cells in culture through an Akt-dependent pathway. Endocrinology 150:929-35
Palaniappan, Murugesan; Menon, K M J (2009) Regulation of sterol regulatory element-binding transcription factor 1a by human chorionic gonadotropin and insulin in cultured rat theca-interstitial cells. Biol Reprod 81:284-92
Kayampilly, Pradeep P; Menon, K M J (2007) Follicle-stimulating hormone increases tuberin phosphorylation and mammalian target of rapamycin signaling through an extracellular signal-regulated kinase-dependent pathway in rat granulosa cells. Endocrinology 148:3950-7

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