Open Access
Numéro |
Med Sci (Paris)
Volume 37, Numéro 4, Avril 2021
|
|
---|---|---|
Page(s) | 366 - 371 | |
Section | M/S Revues | |
DOI | https://doi.org/10.1051/medsci/2021035 | |
Publié en ligne | 28 avril 2021 |
- Boehm U, Bouloux PM, Dattani MT, et al. Expert consensus document: European consensus statement on congenital hypogonadotropic hypogonadism–pathogenesis, diagnosis and treatment. Nat Rev Endocrinol 2015 ; 11 : 547–564. [CrossRef] [PubMed] [Google Scholar]
- Howard SR, Dunkel L. Delayed puberty-phenotypic diversity, molecular genetic mechanisms, and recent discoveries. Endocr Rev 2019 ; 40 : 1285–1317. [CrossRef] [PubMed] [Google Scholar]
- Parent AS, Teilmann G, Juul A, et al. The timing of normal puberty and the age limits of sexual precocity: variations around the world, secular trends, and changes after migration. Endocr Rev 2003 ; 24 : 668–693. [CrossRef] [PubMed] [Google Scholar]
- Schwanzel-Fukuda M, Pfaff DW. Origin of luteinizing hormone-releasing hormone neurons. Nature 1989 ; 338 : 161–164. [CrossRef] [PubMed] [Google Scholar]
- Wray S, Grant P, Gainer H. Evidence that cells expressing luteinizing hormone-releasing hormone mRNA in the mouse are derived from progenitor cells in the olfactory placode. Proc Natl Acad Sci USA 1989 ; 86 : 8132–8136. [Google Scholar]
- Giacobini P.. Shaping the reproductive system: role of semaphorins in gonadotropin-releasing hormone development and function. Neuroendocrinology 2015 ; 102 : 200–215. [CrossRef] [PubMed] [Google Scholar]
- Imai T, Yamazaki T, Kobayakawa R, et al. Pre-target axon sorting establishes the neural map topography. Science 2009 ; 325 : 585–590. [CrossRef] [PubMed] [Google Scholar]
- Casoni F, Malone SA, Belle M, et al. Development of the neurons controlling fertility in humans: new insights from 3D imaging and transparent fetal brains. Development 2016 ; 143 : 3969–3981. [CrossRef] [PubMed] [Google Scholar]
- Vanacker C, Trova S, Shruti S, et al. Neuropilin-1 expression in GnRH neurons regulates prepubertal weight gain and sexual attraction. EMBO J 2020; 39 : e104633. [CrossRef] [PubMed] [Google Scholar]
- Hanchate NK, Giacobini P, Lhuillier P, et al. SEMA3A, a Gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome. PLoS Genet 2012 ; 8 : e1002896. [CrossRef] [PubMed] [Google Scholar]
- Marcos S, Monnier C, Rovira X, et al. Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice. Hum Mol Genet 2017 ; 26 : 2006–2017. [CrossRef] [PubMed] [Google Scholar]
- Kotan LD, Ternier G, Cakir AD, et al. Loss-of-function mutations in sema3f and plxna3 encoding semaphorin-3F and its receptor Plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism. Genet Med 2021. doi: 10.1038/s41436-020-01087-5. [PubMed] [Google Scholar]
- Van der Klaauw AA, Croizier S, Mendes de Oliveira E, et al. Human semaphorin 3 variants link melanocortin circuit development and energy balance. Cell 2019; 176 : 729–42e18. [CrossRef] [PubMed] [Google Scholar]
- Wehner AB, Abdesselem H, Dickendesher TL, et al. Semaphorin 3A is a retrograde cell death signal in developing sympathetic neurons. Development 2016 ; 143 : 1560–1570. [CrossRef] [PubMed] [Google Scholar]
- Orr BO, Fetter RD, Davis GW. Retrograde semaphorin-plexin signalling drives homeostatic synaptic plasticity. Nature 2017 ; 550 : 109–113. [CrossRef] [PubMed] [Google Scholar]
- Howard SR, Guasti L, Ruiz-Babot G, et al. IGSF10 mutations dysregulate gonadotropin-releasing hormone neuronal migration resulting in delayed puberty. EMBO Mol Med 2016 ; 8 : 626–642. [CrossRef] [PubMed] [Google Scholar]
- Abreu AP, Dauber A, Macedo DB, et al. Central precocious puberty caused by mutations in the imprinted gene MKRN3. N Engl J Med 2013 ; 368 : 2467–2475. [CrossRef] [PubMed] [Google Scholar]
- Abreu AP, Toro CA, Song YB, et al. MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons. J Clin Invest 2020; 130 : 4486–500. [PubMed] [Google Scholar]
- Heras V, Sangiao-Alvarellos S, Manfredi-Lozano M, et al. Hypothalamic miR-30 regulates puberty onset via repression of the puberty-suppressing factor, Mkrn3. PLoS Biol 2019 ; 17 : e3000532. [CrossRef] [PubMed] [Google Scholar]
- Dauber A, Cunha-Silva M, Macedo DB, et al. Paternally inherited DLK1 deletion associated with familial central precocious puberty. J Clin Endocrinol Metab 2017 ; 102 : 1557–1567. [CrossRef] [PubMed] [Google Scholar]
- Silveira LG, Noel SD, Silveira-Neto AP, et al. Mutations of the KISS1 gene in disorders of puberty. J Clin Endocrinol Metab 2010 ; 95 : 2276–2280. [CrossRef] [PubMed] [Google Scholar]
- Teles MG, Bianco SD, Brito VN, et al. A GPR54-activating mutation in a patient with central precocious puberty. N Engl J Med 2008 ; 358 : 709–715. [CrossRef] [PubMed] [Google Scholar]
- Ahmed ML, Ong KK, Morrell DJ, et al. Longitudinal study of leptin concentrations during puberty: sex differences and relationship to changes in body composition. J Clin Endocrinol Metab 1999 ; 84 : 899–905. [PubMed] [Google Scholar]
- Prevot V. Puberty in mice and rats. In : Plant TM, Zeleznik J, eds. Knobil and Neill’s physiology of reproduction. New York: Elsevier, 2015 : 1395–1439. [Google Scholar]
- Tena-Sempere M. Physiological mechanisms for the metabolic control of reproduction. In : Plant TM, Zeleznik J Knobil and Neill’s physiology of reproduction. New York: Elsevier, 2015: 1605–1636. [Google Scholar]
- He Q, Karlberg J. Bmi in childhood and its association with height gain, timing of puberty, and final height. Pediatr Res 2001 ; 49 : 244–251. [CrossRef] [PubMed] [Google Scholar]
- McKinney TD, Desjardins C. Postnatal development of the testis, fighting behavior, and fertility in house mice. Biol Reprod 1973 ; 9 : 279–294. [CrossRef] [PubMed] [Google Scholar]
- Hess RA, Renato de Franca L. Spermatogenesis and cycle of the seminiferpus epithelium. In: Cheng CY, ed. Molecular mechanisms in spermatogenesis. New York : Springer-Verlag, 2008 : 1–15. [Google Scholar]
- McGee SR, Narayan P. Precocious puberty and Leydig cell hyperplasia in male mice with a gain of function mutation in the LH receptor gene. Endocrinology 2013 ; 154 : 3900–3913. [CrossRef] [PubMed] [Google Scholar]
- Giger RJ, Wolfer DP, De Wit GM, Verhaagen J. Anatomy of rat semaphorin III/collapsin-1 mRNA expression and relationship to developing nerve tracts during neuroembryogenesis. J Comp Neurol 1996 ; 375 : 378–392. [CrossRef] [PubMed] [Google Scholar]
- Dluzen DE, Ramirez VD, Carter CS, Getz LL. Male vole urine changes luteinizing hormone-releasing hormone and norepinephrine in female olfactory bulb. Science 1981 ; 212 : 573–575. [CrossRef] [PubMed] [Google Scholar]
- Boehm U, Zou Z, Buck LB. Feedback loops link odor and pheromone signaling with reproduction. Cell 2005 ; 123 : 683–695. [CrossRef] [PubMed] [Google Scholar]
- Hellier V, Brock O, Candlish M, et al. Female sexual behavior in mice is controlled by kisspeptin neurons. Nat Commun 2018 ; 9 : 400. [CrossRef] [PubMed] [Google Scholar]
- Messina A, Langlet F, Chachlaki K, et al. A microRNA switch regulates the rise in hypothalamic GnRH production before puberty. Nat Neurosci 2016 ; 19 : 835–844. [CrossRef] [PubMed] [Google Scholar]
- Oboti L, Trova S, Schellino R, et al. Activity dependent modulation of granule cell survival in the accessory olfactory bulb at puberty. Front Neuroanat 2017 ; 11 : 44. [CrossRef] [PubMed] [Google Scholar]
- Golub MS, Collman GW, Foster PM, et al. Public health implications of altered puberty timing. Pediatrics 2008 ; 121(suppl 3): S218–S230. [CrossRef] [PubMed] [Google Scholar]
- Comninos AN, Dhillo WS. Emerging roles of kisspeptin in sexual and emotional brain processing. Neuroendocrinology 2018 ; 106 : 195–202. [CrossRef] [PubMed] [Google Scholar]
- Ferrero DM, Moeller LM, Osakada T, et al. A juvenile mouse pheromone inhibits sexual behaviour through the vomeronasal system. Nature 2013 ; 502 : 368–371. [CrossRef] [PubMed] [Google Scholar]
- Gelstein S, Yeshurun Y, Rozenkrantz L, et al. Human tears contain a chemosignal. Science 2011 ; 331 : 226–230. [CrossRef] [PubMed] [Google Scholar]
- He Z, Tessier-Lavigne M. Neuropilin is a receptor for the axonal chemorepellent Semaphorin III. Cell 1997 ; 90 : 739–751. [CrossRef] [PubMed] [Google Scholar]
- Kolodkin AL, Levengood DV, Rowe EG, et al. Neuropilin is a semaphorin III receptor. Cell 1997 ; 90 : 753–762. [CrossRef] [PubMed] [Google Scholar]
- Tamagnone L, Artigiani S, Chen H, et al. Plexins are a large family of receptors for transmembrane, secreted, and GPI-anchored semaphorins in vertebrates. Cell 1999 ; 99 : 71–80. [CrossRef] [PubMed] [Google Scholar]
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