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      Mapping the Follicle-Stimulating Hormone-Induced Signaling Networks

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          Abstract

          Follicle-stimulating hormone (FSH) is a central regulator of male and female reproductive function. Over the last decade, there has been a growing perception of the complexity associated with FSH-induced cellular signaling. It is now clear that the canonical Gs/cAMP/PKA pathway is not the sole mechanism that must be considered in FSH biological actions. In parallel, consistent with the emerging concept of biased agonism, several examples of ligand-mediated selective signaling pathway activation by gonadotropin receptors have been reported. In this context, it is important to gain an integrative view of the signaling pathways induced by FSH and how they interconnect to form a network. In this review, we propose a first attempt at building topological maps of various pathways known to be involved in the FSH-induced signaling network. We discuss the multiple facets of FSH-induced signaling and how they converge to the hormone integrated biological response. Despite of their incompleteness, these maps of the FSH-induced signaling network represent a first step toward gaining a system-level comprehension of this hormone’s actions, which may ultimately facilitate the discovery of novel regulatory processes and therapeutic strategies for infertility and non-steroidal contraception.

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          Most cited references111

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          Transduction of receptor signals by beta-arrestins.

          The transmission of extracellular signals to the interior of the cell is a function of plasma membrane receptors, of which the seven transmembrane receptor family is by far the largest and most versatile. Classically, these receptors stimulate heterotrimeric G proteins, which control rates of generation of diffusible second messengers and entry of ions at the plasma membrane. Recent evidence, however, indicates another previously unappreciated strategy used by the receptors to regulate intracellular signaling pathways. They direct the recruitment, activation, and scaffolding of cytoplasmic signaling complexes via two multifunctional adaptor and transducer molecules, beta-arrestins 1 and 2. This mechanism regulates aspects of cell motility, chemotaxis, apoptosis, and likely other cellular functions through a rapidly expanding list of signaling pathways.
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            Teaching old receptors new tricks: biasing seven-transmembrane receptors.

            Seven-transmembrane receptors (7TMRs; also known as G protein-coupled receptors) are the largest class of receptors in the human genome and are common targets for therapeutics. Originally identified as mediators of 7TMR desensitization, beta-arrestins (arrestin 2 and arrestin 3) are now recognized as true adaptor proteins that transduce signals to multiple effector pathways. Signalling that is mediated by beta-arrestins has distinct biochemical and functional consequences from those mediated by G proteins, and several biased ligands and receptors have been identified that preferentially signal through either G protein- or beta-arrestin-mediated pathways. These ligands are not only useful tools for investigating the biochemistry of 7TMR signalling, they also have the potential to be developed into new classes of therapeutics.
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              Follicle stimulating hormone is required for ovarian follicle maturation but not male fertility.

              Follicle stimulating hormone (FSH) is a member of the glycoprotein hormone family that includes luteinzing hormone (LH), thyroid stimulating hormone, and chorionic gonadotropin. These heterodimeric hormones share a common alpha subunit and differ in their hormone-specific beta subunit. The biological activity is conferred only by the heterodimers. FSH and LH are synthesized in the same cells of the pituitary, the gonadotrophs. FSH receptors are localized to Sertoli cells of the testes and granulosa cells of the ovary. Minimal data has been accumulated so far involving human mutations in the FSH beta, LH beta, or the gonadotropin receptor genes. There are no known mouse strains with mutations in the FSH beta gene. To generate animal models for human diseases involving the gonadotropin signal transduction pathway, we produced mice deficient in the FSH beta subunit and therefore in FSH using ES cell technology. FSH-deficient females are infertile due to a block in folliculogenesis prior to antral follicle formation. Although FSH was predicted to be necessary for spermatogenesis and Sertoli cell growth in males, FSH-deficient males are fertile despite having small testes. Our findings have important implications for male contraceptive development in humans.
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                Author and article information

                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrin.
                Frontiers in Endocrinology
                Frontiers Research Foundation
                1664-2392
                05 October 2011
                2011
                : 2
                : 45
                Affiliations
                [1] 1simpleBIOS Group, INRA, UMR85, Unité Physiologie de la Reproduction et des Comportements Nouzilly, France
                [2] 2simpleUMR6175, CNRS Nouzilly, France
                [3] 3simpleUniversité François Rabelais Tours, France
                [4] 4simpleL’Institut Français du Cheval et de l’Équitation Nouzilly, France
                Author notes

                Edited by: Sandhya Srikant Visweswariah, Indian Institute of Science, India

                Reviewed by: Suraj Unniappan, York University, Canada; Rajan R. Dighe, Indian Institute of Science, India

                *Correspondence: Eric Reiter, INRA UMR85, CNRS-Université François Rabelais UMR6175, 37380, Nouzilly, France. e-mail: Eric.Reiter@ 123456tours.inra.fr

                This article was submitted to Frontiers in Cellular Endocrinology, a specialty of Frontiers in Endocrinology.

                Article
                10.3389/fendo.2011.00045
                3364461
                22666216
                b06de4a9-9207-4dbd-bb0d-014e4cdb7501
                Copyright © 2011 Gloaguen, Crépieux, Heitzler, Poupon and Reiter.

                This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.

                History
                : 13 July 2011
                : 14 September 2011
                Page count
                Figures: 7, Tables: 0, Equations: 0, References: 106, Pages: 13, Words: 9204
                Categories
                Endocrinology
                Review Article

                Endocrinology & Diabetes
                systems biology,receptor,topological map,signaling network,follicle-stimulating hormone

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