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Essay, 8 pages (1900 words)

Editorial: progress in reproductive neuroendocrinology in vertebrates

Editorial on the Research Topic
Progress in Reproductive Neuroendocrinology in Vertebrates

The hypothalamic-pituitary-gonadal (HPG) axis is imperative in the control of reproduction in vertebrates. It was thought that gonadotropin-releasing hormone (GnRH) was the only hypothalamic neuropeptide that regulates the HPG axis since its discovery at the beginning of the 1970s ( 1 , 2 ). However, two new key hypothalamic neuropeptides, i. e., gonadotropin-inhibitory hormone (GnIH) and kisspeptin, have been found in the beginning of the 2000s to play key roles in the control of reproduction ( 3 6 ). In 2000, GnIH was discovered in the quail hypothalamus ( 3 ). Following intensive researches showed that GnIH inhibits gonadotropin synthesis and release through actions on GnRH neurons and gonadotropes via a G-protein coupled receptor (GPCR), GPR147, in birds and mammals ( 7 ). GnIH peptides were also identified in other vertebrate species from fish to humans. As in birds, mammalian and fish GnIH peptides inhibit gonadotropin release, indicating the conserved inhibitory role of GnIH in the regulation of the HPG axis ( 7 ). Following the discovery of GnIH, kisspeptin, encoded by the Kiss1 gene, was discovered in mammals. In contrast to GnIH, kisspeptin has a stimulatory effect on GnRH neurons via another GPCR, GPR54 ( 5 , 6 ). The Kiss1 gene was also identified in amphibians and fish ( 8 ). Therefore, we now know that GnRH is not the only hypothalamic neuropeptide controlling reproduction in vertebrates. The aim of this flagship Research Topic is to review the discoveries of GnIH and kisspeptin and the progress in reproductive neuroendocrinology made by these hypothalamic neuropeptides by collecting review articles from leading scientists in this new research field.

The first review article by Tsutsui and Ubuka summarizes the discovery of GnIH and progresses of GnIH research. GnIH was isolated and its structure was determined in 2000 ( 3 ). Its function that inhibits gonadotropin release was shown in quail in vitro ( 3 ) and in vivo ( 4 ). The article introduces that GnIH inhibits gonadotropin synthesis and release from gonadotropes by acting on gonadotropes and GnRH neurons via GPR147 ( 9 , 10 ). The article also reviews that GnIH acts in the brain to regulate various behaviors ( 11 13 ). The second review article by Son et al. describes the molecular mechanisms of GnIH actions in target cells and how GnIH expression is regulated. Based on the morphology of GnIH neuronal fibers and GnIH receptor, GnRH neurons and gonadotropes are the major targets of GnIH action ( 3 , 14 17 ). It was demonstrated that GnIH inhibits the adenylate cyclase (AC)/cAMP/protein kinase A (PKA)-dependent pathway both in GnRH neurons and gonadotropes ( 9 , 10 ). The article further summarizes the mechanisms of how GnIH expression is regulated by glucocorticoid ( 18 ) and thyroid hormone ( 19 ). The third review article by Angelopoulou et al. introduces that RFRP-3, mammalian GnIH, is involved in the central control of daily and seasonal rhythms of reproduction to synchronize reproductive activity to environmental challenges. Melatonin and thyroid hormones may play critical roles in the regulation of GnIH neurons that convey environmental information to GnRH neurons and gonadotropes ( 17 , 20 23 ). The fourth review article by Tobari and Tsutsui introduces the effects of social information on GnIH in birds ( 13 ). The article reviews researches that investigates the changes in the activities of GnIH neuronal system according to social status. The article introduces the pathway after visual perception of a potential mate and the rapid change in gonadotropin levels via the GnIH neuronal system in male birds. The fifth review article by Di Yorio et al. summarizes what are known and unknown about fish GnIH ( 24 , 25 ). The article emphasizes that teleost is characterized by three round whole genome duplication that could be responsible for the great phenotypic complexity and variability in reproductive strategies and sexual behavior. The fact may also affect the distribution of GnIH cell bodies and fibers and its relationship with GnRH variants. The article proposes that GnIH may have other functions than reproduction or act as an integrator in the reproductive process in teleosts. The last review article by Uenoyama et al. introduces the triggering role of kisspeptin that controls pubertal onset in mammals. Kisspeptin is a potent secretagogue of GnRH secretion therefore its release is fundamental to pubertal increase in GnRH/gonadotropin secretion. It is thought that puberty is timed by an increase in pulsatile GnRH/gonadotropin secretion in mammals. Recent researches suggest that kisspeptin/neurokinin B/dynorphin A (KNDy) neurons in the arcuate nucleus may play an important role in pulsatile GnRH/gonadotropin secretin during pubertal onset ( 26 ). The article further suggests that the timing of pubertal onset is controlled by upstream regulators of kisspeptin expression and release.

The review articles collected in this flagship Research Topic acknowledge that GnIH and kisspeptin play important roles in the hypothalamic control of reproduction, which is indispensable in developmental, seasonal, and social regulation of reproductive activities in vertebrates.

Author Contributions

TU wrote the manuscript. KT edited the manuscript.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

1. Burgus R, Butcher M, Amoss M, Ling N, Monahan M, Rivier J, et al. Primary structure of the ovine hypothalamic luteinizing hormone-releasing factor (LRF) (LH-hypothalamus-LRF-gas chromatography-mass spectrometry-decapeptide-Edman degradation). Proc Natl Acad Sci USA . (1972) 69: 278–82. doi: 10. 1073/pnas. 69. 1. 278

2. Matsuo H, Baba Y, Nair RM, Arimura A, Schally AV. Structure of the porcineLH- and FSH-releasing hormone. I The proposed amino acid sequence. Biochem Biophys Res Commun . (1971) 43: 1334–9. doi: 10. 1016/S0006-291X(71)80019-0

3. Tsutsui K, Saigoh E, Ukena K, Teranishi H, Fujisawa Y, Kikuchi M, et al. A novel avian hypothalamic peptide inhibiting gonadotropin release. Biochem Biophys Res Commun . (2000) 275: 661–7. doi: 10. 1006/bbrc. 2000. 3350

4. Ubuka T, Ukena K, Sharp PJ, Bentley GE, Tsutsui K. Gonadotropin-inhibitory hormone inhibits gonadal development and maintenance by decreasing gonadotropin synthesis and release in male quail. Endocrinology . (2006) 147: 1187–94. doi: 10. 1210/en. 2005-1178

5. de Roux N, Genin E, Carel JC, Matsuda F, Chaussain JL, Milgrom E. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc Natl Acad Sci USA . (2003) 100: 10972–6. doi: 10. 1073/pnas. 1834399100

6. Seminara SB, Messager S, Chatzidaki EE, Thresher RR, Acierno JS Jr, Shagoury JK, et al. The GPR54 gene as a regulator of puberty. N Engl J Med . (2003) 349: 1614–27. doi: 10. 1056/NEJMoa035322

7. Ubuka T, Son YL, Tsutsui K. Molecular, cellular, morphological, physiological and behavioral aspects of gonadotropin-inhibitory hormone. Gen Comp Endocrinol . (2016) 227: 27–50. doi: 10. 1016/j. ygcen. 2015. 09. 009

8. Lee YR, Tsunekawa K, Moon MJ, Um HN, Hwang JI, Osugi T, et al. Molecular evolution of multiple forms of kisspeptins and GPR54 receptors in vertebrates. Endocrinology . (2009) 150: 2837–46. doi: 10. 1210/en. 2008-1679

9. Son YL, Ubuka T, Millar RP, Kanasaki H, Tsutsui K. Gonadotropin-inhibitory hormone inhibits GnRH-induced gonadotropin subunit gene transcriptions by inhibiting AC/cAMP/PKA-dependent ERK pathway in LβT2 cells. Endocrinology . (2012) 153: 2332–43. doi: 10. 1210/en. 2011-1904

10. Son YL, Ubuka T, Soga T, Yamamoto K, Bentley GE, Tsutsui K. Inhibitory action of gonadotropin-inhibitory hormone on the signaling pathways induced by kisspeptin and vasoactive intestinal polypeptide in GnRH neuronal cell line, GT1-7. FASEB J . (2016) 30: 2198–210. doi: 10. 1096/fj. 201500055

11. Ubuka T, Mukai M, Wolfe J, Beverly R, Clegg S, Wang A, et al. RNA interference of gonadotropin-inhibitory hormone gene induces arousal in songbirds. PLoS ONE . (2012) 7: e30202. doi: 10. 1371/journal. pone. 0030202

12. Ubuka T, Haraguchi S, Tobari Y, Narihiro M, Ishikawa K, Hayashi T, et al. Hypothalamic inhibition of socio-sexual behaviour by increasing neuroestrogen synthesis. Nat Commun . (2014) 5: 3061. doi: 10. 1038/ncomms4061

13. Tobari Y, Son YL, Ubuka T, Hasegawa Y, Tsutsui K. A new pathway mediating social effects on the endocrine system: female presence acting via norepinephrine release stimulates gonadotropin-inhibitory hormone in the paraventricular nucleus and suppresses luteinizing hormone in quail. J Neurosci . (2014) 34: 9803–11. doi: 10. 1523/JNEUROSCI. 3706-13. 2014

14. Ubuka T, Kim S, Huang YC, Reid J, Jiang J, Osugi T, et al. Gonadotropin-inhibitory hormone neurons interact directly with gonadotropin-releasing hormone-I and -II neurons in European starling brain. Endocrinology . (2008) 149: 268–78. doi: 10. 1210/en. 2007-0983

15. Ubuka T, Lai H, Kitani M, Suzuuchi A, Pham V, Cadigan PA, et al. Gonadotropin-inhibitory hormone identification, cDNA cloning, and distribution in rhesus macaque brain. J Comp Neurol . (2009) 517: 841–55. doi: 10. 1002/cne. 22191

16. Ubuka T, Morgan K, Pawson AJ, Osugi T, Chowdhury VS, Minakata H, et al. Identification of human GnIH homologs, RFRP-1 and RFRP-3, and the cognate receptor, GPR147 in the human hypothalamic pituitary axis. PLoS ONE . (2009) 4: e8400. doi: 10. 1371/journal. pone. 0008400

17. Ubuka T, Inoue K, Fukuda Y, Mizuno T, Ukena K, Kriegsfeld LJ, et al. Identification, expression, and physiological functions of Siberian hamster gonadotropin-inhibitory hormone. Endocrinology . (2012) 153: 373–85. doi: 10. 1210/en. 2011-1110

18. Son YL, Ubuka T, Narihiro M, Fukuda Y, Hasunuma I, Yamamoto K, et al. Molecular basis for the activation of gonadotropin-inhibitory hormone gene transcription by corticosterone. Endocrinology . (2014) 155: 1817–26. doi: 10. 1210/en. 2013-2076

19. Kiyohara M, Son YL, Tsutsui K. Involvement of gonadotropin-inhibitory hormone in pubertal disorders induced by thyroid status. Sci Rep.(2017) 7: 1042. doi: 10. 1038/s41598-017-01183-8

20. Ubuka T, Bentley GE, Ukena K, Wingfield JC, Tsutsui K. Melatonin induces the expression of gonadotropin-inhibitory hormone in the avian brain. Proc Natl Acad Sci USA.(2005) 102: 3052–7. doi: 10. 1073/pnas. 0403840102

21. Klosen P, Bienvenu C, Demarteau O, Dardente H, Guerrero H, Pévet P, et al. The mt1 melatonin receptor and RORbeta receptor are co-localized in specific TSH-immunoreactive cells in the pars tuberalis of the rat pituitary. J Histochem Cytochem . (2002) 50: 1647–57. doi: 10. 1177/002215540205001209

22. Dardente H, Wyse CA, Birnie MJ, Dupré SM, Loudon ASI, Lincoln GA, et al. A molecular switch for photoperiod responsiveness in mammals. Curr Biol . (2010) 20: 2193–8. doi: 10. 1016/j. cub. 2010. 10. 048

23. Klosen P, Sébert M-E, Rasri K, Laran-Chich M-P, Simonneaux V. TSH restores a summer phenotype in photoinhibited mammals via the RF-amides RFRP3 and kisspeptin. FASEB J . (2013) 27: 2677–86. doi: 10. 1096/fj. 13-229559

24. Ubuka T, Parhar I. Dual actions of mammalian and piscine gonadotropin-inhibitory hormones, RFamide-related peptides and LPXRFamide peptides, in the hypothalamic-pituitary-gonadal axis. Front Endocrinol . (2018). 8: 377. doi: 10. 3389/fendo. 2017. 00377

25. Muñoz-Cueto JA, Paullada-Salmerón JA, Aliaga-Guerrero M, Cowan ME, Parhar IS, Ubuka T. A journey through the gonadotropin-inhibitory hormone system of fish. Front Endocrinol . (2017) 8: 285. doi: 10. 3389/fendo. 2017. 00285

26. Ikegami K, Minabe S, Ieda N, Goto T, Sugimoto A, Nakamura S, et al. Evidence of involvement of neurone-glia/neurone-neurone communications via gap junctions in synchronised activity of KNDy neurones. J Neuroendocrinol . (2017) 29: 1–14. doi: 10. 1111/jne. 12480

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