Published January 1, 2018 | Version Supplemental Material
Journal Article Open

Evolutionally Conserved Function of Kisspeptin Neuronal System Is Nonreproductive Regulation as Revealed by Nonmammalian Study

  • 1. ROR icon University of Tokyo
  • 2. ROR icon California Institute of Technology
  • 3. ROR icon St. Marianna University School of Medicine
  • 4. ROR icon Nagoya University
  • 5. ROR icon International Christian University

Abstract

The kisspeptin neuronal system, which consists of a neuropeptide kisspeptin and its receptor Gpr54, is considered in mammals a key factor of reproductive regulation, the so-called hypothalamic–pituitary–gonadal (HPG) axis. However, in nonmammalian vertebrates, especially in teleosts, existence of kisspeptin regulation on the HPG axis is still controversial. In this study, we applied multidisciplinary techniques to a teleost fish, medaka, and examined possible kisspeptin regulation on the HPG axis. First, we generated knockout medaka for kisspeptin-related genes and found that they show normal fertility, gonadal maturation, and expression of gonadotropins. Moreover, the firing activity of GnRH1 neurons recorded by the patch clamp technique was not altered by kisspeptin application. Furthermore, in goldfish, in vivo kisspeptin administration did not show any positive effect on HPG axis regulation. However, as kisspeptin genes are completely conserved among vertebrates except birds, we surmised that kisspeptin should have some important nonreproductive functions in vertebrates. Therefore, to discover novel functions of kisspeptin, we generated a gpr54-1:enhanced green fluorescent protein (EGFP) transgenic medaka, whose gpr54-1–expressing cells are specifically labeled by EGFP. Analysis of neuronal projection of gpr54-1:EGFP–expressing neurons showed that these neurons in the ventrolateral preoptic area project to the pituitary and are probably involved in endocrine regulation other than gonadotropin release. Furthermore, combination of deep sequencing, histological, and electrophysiological analyses revealed various novel neural systems that are under control of kisspeptin neurons—that is, those expressing neuropeptide Yb, cholecystokinin, isotocin, vasotocin, and neuropeptide B. Thus, our new strategy to genetically label receptor-expressing neurons gives insights into various kisspeptin-dependent neuronal systems that may be conserved in vertebrates.

Additional Information

© 2018 Endocrine Society. Received: 01 September 2017; Accepted: 10 October 2017; Published: 18 October 2017. We thank Dr. Shinya Oishi (Kyoto University) for helpful advice and presenting FTM145, and Dr. Kataaki Okubo (University of Tokyo) and Dr. Towako Kajiyama-Hiraki (RIKEN) for helpful advice and gifts of constructs for npb ISH probes. We also thank Dr. Toyoji Kaneko (University of Tokyo) for helpful advice and for providing the equipment for keeping goldfish. We are grateful to Dr. Buntaro Zempo (Osaka Medical College) for helpful suggestions in ISH protocols. We also thank Martin J. Kelly, Oline K. Rønnekleiv, and Martha Bosch (Oregon Health and Science University) for helpful advice for the cell harvesting procedure for deep sequencing, and Miho Kyokuwa and Hisako Kohno for daily care of the fish used in this study. Thanks are also due to Dr. Takeshi Kaneko (Kyoto University) and Dr. Hiroyuki Hioki (Kyoto University) for providing the anti-EGFP antibody, and to Dr. Hiroshi Hosokawa (Kyoto University) for help in establishing the behavior assays. The RIA was performed at the Nagoya University Radioisotope Center. This work was supported by Grants-in-Aid from Japan Society for the Promotion of Science Grants 15J06435 (to M.N.) and 26840111, a Suntory Foundation for Life Sciences grant (SUNBOR; to S.K.), and Japan Society for the Promotion of Science Grant 26221104, as well as by the Program for Promotion of Basic Research Activities for Innovative Biosciences of Japan (to Y.O.). This work was also supported by Graduate Program for Leaders in Life Innovation (GPLLI), the University of Tokyo Life Innovation Leading Graduate School from MEXT, Japan. The authors have nothing to disclose.

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Additional details

Identifiers

Eprint ID
82772
DOI
10.1210/en.2017-00808
Resolver ID
CaltechAUTHORS:20171030-132156693

Related works

Describes
10.1210/en.2017-00808 (DOI)

Funding

Japan Society for the Promotion of Science (JSPS)
15J06435
Japan Society for the Promotion of Science (JSPS)
26840111
Suntory Foundation for Life Sciences
Japan Society for the Promotion of Science (JSPS)
26221104
Program for Promotion of Basic Research Activities for Innovative Biosciences of Japan
Ministry of Education, Culture, Sports, Science and Technology (MEXT)

Dates

Created
2017-10-30
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Updated
2021-11-15
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