Follicle-stimulating hormone receptor explained

The follicle-stimulating hormone receptor or FSH receptor (FSHR) is a transmembrane receptor that interacts with the follicle-stimulating hormone (FSH) and represents a G protein-coupled receptor (GPCR). Its activation is necessary for the hormonal functioning of FSH. FSHRs are found in the ovary, testis, and uterus.

FSHR gene

The gene for the FSHR is found on chromosome 2 p21 in humans. The gene sequence of the FSHR consists of about 2,080 nucleotides.[1]

Receptor structure

The FSHR consists of 695 amino acids and has a molecular mass of about 76 kDa.[1] Like other GPCRs, the FSH-receptor possesses seven membrane-spanning domains or transmembrane helices.

Ligand binding and signal transduction

Upon initial binding to the LRR region of FSHR, FSH reshapes its conformation to form a new pocket. FSHR then inserts its sulfotyrosine from the hinge loop into the pockets and activates the 7-helical transmembrane domain.[2] This event leads to a transduction of the signal that activates the Gs protein that is bound to the receptor internally. With FSH attached, the receptor shifts conformation and, thus, mechanically activates the G protein, which detaches from the receptor and activates the cAMP system.[5] [6]

It is believed that a receptor molecule exists in a conformational equilibrium between active and inactive states. The binding of FSH to the receptor shifts the equilibrium between active and inactive receptors. FSH and FSH-agonists shift the equilibrium in favor of active states; FSH antagonists shift the equilibrium in favor of inactive states.

Phosphorylation by cAMP-dependent protein kinases

Cyclic AMP-dependent protein kinases (protein kinase A) are activated by the signal chain coming from the Gs protein (that was activated by the FSH-receptor) via adenylate cyclase and cyclic AMP (cAMP).[5] [6]

These protein kinases are present as tetramers with two regulatory units and two catalytic units. Upon binding of cAMP to the regulatory units, the catalytic units are released and initiate the phosphorylation of proteins, leading to the physiologic action. The cyclic AMP-regulatory dimers are degraded by phosphodiesterase and release 5’AMP. DNA in the cell nucleus binds to phosphorylated proteins through the cyclic AMP response element (CRE), which results in the activation of genes.[1]

The signal is amplified by the involvement of cAMP and the resulting phosphorylation. The process is modified by prostaglandins. Other cellular regulators are participate are the intracellular calcium concentration modified by phospholipase, nitric acid, and other growth factors.

The FSH receptor can also activate the extracellular signal-regulated kinases (ERK).[7] In a feedback mechanism, these activated kinases phosphorylate the receptor.

Action

In the ovary, the FSH receptor is necessary for follicular development and expressed on the granulosa cells.[1]

In the male, the FSH receptor has been identified on the Sertoli cells that are critical for spermatogenesis.[8]

The FSHR is expressed during the luteal phase in the secretory endometrium of the uterus.[9]

FSH receptor is selectively expressed on the surface of the blood vessels of a wide range of carcinogenic tumors.[10]

Receptor regulation

Upregulation

Upregulation refers to the increase in the number of receptor sites on the membrane. Estrogen upregulates FSH receptor sites. In turn, FSH stimulates granulosa cells to produce estrogens. This synergistic activity of estrogen and FSH allows for follicle growth and development in the ovary.

Desensitization

The FSHR become desensitized when exposed to FSH for some time. A key reaction of this downregulation is the phosphorylation of the intracellular (or cytoplasmic) receptor domain by protein kinases.[11] This process uncouples Gs protein from the FSHR. Another way to desensitize is to uncouple the regulatory and catalytic units of the cAMP system.

Downregulation

Downregulation refers to the decrease in the number of receptor sites. This can be accomplished by metabolizing bound FSHR sites. The bound FSH-receptor complex is brought by lateral migration to a "coated pit," where such units are concentrated and then stabilized by a framework of clathrins. A pinched-off coated pit is internalized and degraded by lysosomes. Proteins may be metabolized or the receptor can be recycled.

Modulators

Antibodies to FSHR can interfere with FSHR activity.

FSH abnormalities

Some patients with ovarian hyperstimulation syndrome may have mutations in the gene for FSHR, making them more sensitive to gonadotropin stimulation.[12]

Women with 46 XX gonadal dysgenesis experience primary amenorrhea with hypergonadotropic hypogonadism. There are forms of 46 xx gonadal dysgenesis wherein abnormalities in the FSH-receptor have been reported and are thought to be the cause of the hypogonadism.[13]

Polymorphism may affect FSH receptor populations and lead to poorer responses in infertile women receiving FSH medication for IVF.[14]

Alternative splicing of the FSHR gene may be implicated in subfertility in males[15]

Ligands

Follicle-stimulating hormone (FSH) is an agonist of the FSHR.

Small-molecule positive allosteric modulators of the FSHR have been developed.[16]

History

Alfred G. Gilman and Martin Rodbell received the 1994 Nobel Prize in Medicine and Physiology for "their discovery of G-proteins and the role of these proteins in signal transduction in cells".[17] [18]

See also

Notes and References

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  2. Jiang X, Liu H, Chen X, Chen PH, Fischer D, Sriraman V, Yu HN, Arkinstall S, He X . Structure of follicle-stimulating hormone in complex with the entire ectodomain of its receptor . Proceedings of the National Academy of Sciences of the United States of America . 109 . 31 . 12491–6 . Jul 2012 . 22802634 . 10.1073/pnas.1206643109 . 3411987. 2012PNAS..10912491J . free .
  3. Costagliola S, Panneels V, Bonomi M, Koch J, Many MC, Smits G, Vassart G . Tyrosine sulfation is required for agonist recognition by glycoprotein hormone receptors . The EMBO Journal . 21 . 4 . 504–13 . Feb 2002 . 11847099 . 10.1093/emboj/21.4.504 . 125869.
  4. Jiang X, Dias JA, He X . Structural biology of glycoprotein hormones and their receptors: insights to signaling . Molecular and Cellular Endocrinology . 382 . 1 . 424–51 . Jan 2014 . 24001578 . 10.1016/j.mce.2013.08.021 . free .
  5. De Pascali F, Tréfier A, Landomiel F, Bozon V, Bruneau G, Yvinec R, Poupon A, Crépieux P, Reiter E . Follicle-Stimulating Hormone Receptor: Advances and Remaining Challenges . International Review of Cell and Molecular Biology . 338 . 1–58 . 2018 . 29699689 . 10.1016/bs.ircmb.2018.02.001 . 978-0-12-813772-7 . 1808.01965 .
  6. Casarini L, Crépieux P . Molecular Mechanisms of Action of FSH . Frontiers in Endocrinology . 10 . 305 . 2019 . 31139153 . 10.3389/fendo.2019.00305 . free . 11380/1181065 . free .
  7. Piketty V, Kara E, Guillou F, Reiter E, Crepieux P . Follicle-stimulating hormone (FSH) activates extracellular signal-regulated kinase phosphorylation independently of beta-arrestin- and dynamin-mediated FSH receptor internalization . Reproductive Biology and Endocrinology . 4 . 33 . 2006 . 16787538 . 1524777 . 10.1186/1477-7827-4-33 . free .
  8. Asatiani K, Gromoll J, Eckardstein SV, Zitzmann M, Nieschlag E, Simoni M . Distribution and function of FSH receptor genetic variants in normal men . Andrologia . 34 . 3 . 172–6 . Jun 2002 . 12059813 . 10.1046/j.1439-0272.2002.00493.x . 21090038 . free .
  9. La Marca A, Carducci Artenisio A, Stabile G, Rivasi F, Volpe A . Evidence for cycle-dependent expression of follicle-stimulating hormone receptor in human endometrium . Gynecological Endocrinology . 21 . 6 . 303–6 . Dec 2005 . 16390776 . 10.1080/09513590500402756 . 24690912 .
  10. Radu A, Pichon C, Camparo P, Antoine M, Allory Y, Couvelard A, Fromont G, Hai MT, Ghinea N . Expression of follicle-stimulating hormone receptor in tumor blood vessels . The New England Journal of Medicine . 363 . 17 . 1621–30 . Oct 2010 . 20961245 . 10.1056/NEJMoa1001283 . free .
  11. Manna PR, Pakarainen P, Rannikko AS, Huhtaniemi IT . Mechanisms of desensitization of follicle-stimulating hormone (FSH) action in a murine granulosa cell line stably transfected with the human FSH receptor complementary deoxyribonucleic acid . Molecular and Cellular Endocrinology . 146 . 1-2 . 163–176 . November 1998 . 10022774 . 10.1016/S0303-7207(98)00156-7 .
  12. Delbaere A, Smits G, De Leener A, Costagliola S, Vassart G . Understanding ovarian hyperstimulation syndrome . Endocrine . 26 . 3 . 285–90 . Apr 2005 . 16034183 . 10.1385/ENDO:26:3:285 . 7607365 .
  13. Aittomäki K, Lucena JL, Pakarinen P, Sistonen P, Tapanainen J, Gromoll J, Kaskikari R, Sankila EM, Lehväslaiho H, Engel AR, Nieschlag E, Huhtaniemi I, de la Chapelle A . Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure . Cell . 82 . 6 . 959–68 . Sep 1995 . 7553856 . 10.1016/0092-8674(95)90275-9 . 14748261 . free .
  14. Loutradis D, Patsoula E, Minas V, Koussidis GA, Antsaklis A, Michalas S, Makrigiannakis A . FSH receptor gene polymorphisms have a role for different ovarian response to stimulation in patients entering IVF/ICSI-ET programs . Journal of Assisted Reproduction and Genetics . 23 . 4 . 177–84 . Apr 2006 . 16758348 . 3454958 . 10.1007/s10815-005-9015-z .
  15. Song GJ, Park YS, Lee YS, Lee CC, Kang IS . Mar 2002 . Alternatively spliced variants of the follicle-stimulating hormone receptor gene in the testis of infertile men . Fertility and Sterility . 77 . 3 . 499–504. 10.1016/s0015-0282(01)03221-6 . 11872202 . free .
  16. Nataraja S, Yu H, Guner J, Palmer S . Discovery and Preclinical Development of Orally Active Small Molecules that Exhibit Highly Selective Follicle Stimulating Hormone Receptor Agonism . Front Pharmacol . 11 . 602593 . 2020 . 33519465 . 7845544 . 10.3389/fphar.2020.602593 . free .
  17. Web site: Gilman AG . G Proteins and Regulation of Adenylyl Cyclase . Nobel Lecture . 1994 .
  18. Rodbell M . Signal Transduction: Evolution of an Idea . Nobel Lecture . 1994 .