J García-Ortega1, F M Pinto2, M Fernández-Sánchez1, N Prados1, A Cejudo-Román2, T A Almeida3, M Hernández3, M Romero4, M Tena-Sempere5, L Candenas6. 1. Instituto Valenciano de Infertilidad, Seville, Spain. 2. Instituto de Investigaciones Químicas, CSIC, Seville, Spain. 3. Instituto de Enfermedades Tropicales y Salud Publica, Universidad de La Laguna, Tenerife, Canary Islands. 4. Departamento de Biología Celular, Fisiología e Inmunología, Universidad de Cordoba, Cordoba, Spain CIBER Fisiopatología de la Obesidad y la Nutrición, Cordoba, Spain ISCiii and Instituto Maimónides de Investigación Biomédica de Córdoba/Hospital Universitario Reina Sofia, Cordoba, Spain. 5. Departamento de Biología Celular, Fisiología e Inmunología, Universidad de Cordoba, Cordoba, Spain CIBER Fisiopatología de la Obesidad y la Nutrición, Cordoba, Spain ISCiii and Instituto Maimónides de Investigación Biomédica de Córdoba/Hospital Universitario Reina Sofia, Cordoba, Spain luzcandenas@iiq.csic.es fi1tesem@uco.es. 6. Instituto de Investigaciones Químicas, CSIC, Seville, Spain luzcandenas@iiq.csic.es fi1tesem@uco.es.
Abstract
STUDY QUESTION: Are neurokinin B (NKB), NK3 receptor (NK3R), kisspeptin (KISS1) and kisspeptin receptor (KISS1R) expressed in human ovarian granulosa cells? SUMMARY ANSWER: The NKB/NK3R and kisspeptin/KISS1R systems are co-expressed and functionally active in ovarian granulosa cells. WHAT IS KNOWN ALREADY: The NKB/NK3R and KISS1/KISS1R systems are essential for reproduction. In addition to their well-recognized role in hypothalamic neurons, these peptide systems may contribute to the control of fertility by acting directly on the gonads, but such a direct gonadal role remains largely unknown. STUDY DESIGN, SIZE, DURATION: This study analyzed matched mural granulosa cells (MGCs) and cumulus cells (CCs) collected from preovulatory follicles of oocyte donors at the time of oocyte retrieval. PARTICIPANTS/MATERIALS, SETTING, METHODS: The samples were provided by 56 oocyte donor women undergoing ovarian stimulation treatment. Follicular fluid samples containing MGCs and cumulus-oocyte complexes were collected after transvaginal ultrasound-guided oocyte retrieval. RT-PCR, quantitative real-time PCR, immunocytochemistry and western blot were used to investigate the pattern of expression of the NKB/NK3R and KISS/KISS1R systems in MGCs and CCs. Intracellular free Ca(2+) levels, [Ca(2+)]i, in MGCs after exposure to NKB or KISS1, in the presence or not of tachykinin receptor antagonists, were also measured. MAIN OUTCOME AND THE ROLE OF CHANCE: NKB/NK3R and KISS1/KISS1R systems were expressed, at the mRNA and protein levels, in MGCs and CCs, with significantly higher expression in CCs. Kisspeptin increased the [Ca(2+)]i in the cytosol of human MGCs while exposure to NKB failed to induce any change in [Ca(2+)]i. However, the [Ca(2+)]i response to kisspeptin was reduced in the presence of NKB. The inhibitory effect of NKB was only partially mimicked by the NK3R agonist, senktide and marginally suppressed by the NK3R-selective antagonist SB 222200. Yet, a cocktail of antagonists selective for the NK1, NK2 and NK3 receptors blocked the effect of NKB. LIMITATIONS, REASONS FOR CAUTION: The granulosa and cumulus cells were obtained from oocyte donors undergoing ovarian stimulation, which in comparison with natural cycles, may have affected gene and protein expression in granulosa cells. WIDER IMPLICATIONS OF THE FINDINGS: Our data demonstrate that, in addition to their indispensable effects at the central nervous system, the NKB/NK3R and kisspeptin/KISS1R systems are co-expressed and are functionally active in non-neuronal reproductive cells of the female gonads, the ovarian granulosa cells. STUDY FUNDING/ COMPETING INTERESTS: This work was supported by grants from Ministerio de Economía y Competitividad (CTQ2011-25564 and BFI2011-25021) and Junta de Andalucía (P08-CVI-04185), Spain. J.G.-O., F.M.P., M.F.-S., N.P., A.C.-R., T.A.A., M.H., M.R., M.T.-S. and L.C. have nothing to declare.
STUDY QUESTION: Are neurokinin B (NKB), NK3 receptor (NK3R), kisspeptin (KISS1) and kisspeptin receptor (KISS1R) expressed in humanovarian granulosa cells? SUMMARY ANSWER: The NKB/NK3R and kisspeptin/KISS1R systems are co-expressed and functionally active in ovarian granulosa cells. WHAT IS KNOWN ALREADY: The NKB/NK3R and KISS1/KISS1R systems are essential for reproduction. In addition to their well-recognized role in hypothalamic neurons, these peptide systems may contribute to the control of fertility by acting directly on the gonads, but such a direct gonadal role remains largely unknown. STUDY DESIGN, SIZE, DURATION: This study analyzed matched mural granulosa cells (MGCs) and cumulus cells (CCs) collected from preovulatory follicles of oocyte donors at the time of oocyte retrieval. PARTICIPANTS/MATERIALS, SETTING, METHODS: The samples were provided by 56 oocyte donorwomen undergoing ovarian stimulation treatment. Follicular fluid samples containing MGCs and cumulus-oocyte complexes were collected after transvaginal ultrasound-guided oocyte retrieval. RT-PCR, quantitative real-time PCR, immunocytochemistry and western blot were used to investigate the pattern of expression of the NKB/NK3R and KISS/KISS1R systems in MGCs and CCs. Intracellular free Ca(2+) levels, [Ca(2+)]i, in MGCs after exposure to NKB or KISS1, in the presence or not of tachykinin receptor antagonists, were also measured. MAIN OUTCOME AND THE ROLE OF CHANCE: NKB/NK3R and KISS1/KISS1R systems were expressed, at the mRNA and protein levels, in MGCs and CCs, with significantly higher expression in CCs. Kisspeptin increased the [Ca(2+)]i in the cytosol of human MGCs while exposure to NKB failed to induce any change in [Ca(2+)]i. However, the [Ca(2+)]i response to kisspeptin was reduced in the presence of NKB. The inhibitory effect of NKB was only partially mimicked by the NK3R agonist, senktide and marginally suppressed by the NK3R-selective antagonist SB 222200. Yet, a cocktail of antagonists selective for the NK1, NK2 and NK3 receptors blocked the effect of NKB. LIMITATIONS, REASONS FOR CAUTION: The granulosa and cumulus cells were obtained from oocyte donors undergoing ovarian stimulation, which in comparison with natural cycles, may have affected gene and protein expression in granulosa cells. WIDER IMPLICATIONS OF THE FINDINGS: Our data demonstrate that, in addition to their indispensable effects at the central nervous system, the NKB/NK3R and kisspeptin/KISS1R systems are co-expressed and are functionally active in non-neuronal reproductive cells of the female gonads, the ovarian granulosa cells. STUDY FUNDING/ COMPETING INTERESTS: This work was supported by grants from Ministerio de Economía y Competitividad (CTQ2011-25564 and BFI2011-25021) and Junta de Andalucía (P08-CVI-04185), Spain. J.G.-O., F.M.P., M.F.-S., N.P., A.C.-R., T.A.A., M.H., M.R., M.T.-S. and L.C. have nothing to declare.
Authors: Karolina Skorupskaite; Jyothis T George; Johannes D Veldhuis; Richard A Anderson Journal: J Clin Endocrinol Metab Date: 2018-01-01 Impact factor: 5.958
Authors: Felix R Day; Katherine S Ruth; Deborah J Thompson; Kathryn L Lunetta; Natalia Pervjakova; Daniel I Chasman; Lisette Stolk; Hilary K Finucane; Patrick Sulem; Brendan Bulik-Sullivan; Tõnu Esko; Andrew D Johnson; Cathy E Elks; Nora Franceschini; Chunyan He; Elisabeth Altmaier; Jennifer A Brody; Lude L Franke; Jennifer E Huffman; Margaux F Keller; Patrick F McArdle; Teresa Nutile; Eleonora Porcu; Antonietta Robino; Lynda M Rose; Ursula M Schick; Jennifer A Smith; Alexander Teumer; Michela Traglia; Dragana Vuckovic; Jie Yao; Wei Zhao; Eva Albrecht; Najaf Amin; Tanguy Corre; Jouke-Jan Hottenga; Massimo Mangino; Albert V Smith; Toshiko Tanaka; Goncalo Abecasis; Irene L Andrulis; Hoda Anton-Culver; Antonis C Antoniou; Volker Arndt; Alice M Arnold; Caterina Barbieri; Matthias W Beckmann; Alicia Beeghly-Fadiel; Javier Benitez; Leslie Bernstein; Suzette J Bielinski; Carl Blomqvist; Eric Boerwinkle; Natalia V Bogdanova; Stig E Bojesen; Manjeet K Bolla; Anne-Lise Borresen-Dale; Thibaud S Boutin; Hiltrud Brauch; Hermann Brenner; Thomas Brüning; Barbara Burwinkel; Archie Campbell; Harry Campbell; Stephen J Chanock; J Ross Chapman; Yii-Der Ida Chen; Georgia Chenevix-Trench; Fergus J Couch; Andrea D Coviello; Angela Cox; Kamila Czene; Hatef Darabi; Immaculata De Vivo; Ellen W Demerath; Joe Dennis; Peter Devilee; Thilo Dörk; Isabel Dos-Santos-Silva; Alison M Dunning; John D Eicher; Peter A Fasching; Jessica D Faul; Jonine Figueroa; Dieter Flesch-Janys; Ilaria Gandin; Melissa E Garcia; Montserrat García-Closas; Graham G Giles; Giorgia G Girotto; Mark S Goldberg; Anna González-Neira; Mark O Goodarzi; Megan L Grove; Daniel F Gudbjartsson; Pascal Guénel; Xiuqing Guo; Christopher A Haiman; Per Hall; Ute Hamann; Brian E Henderson; Lynne J Hocking; Albert Hofman; Georg Homuth; Maartje J Hooning; John L Hopper; Frank B Hu; Jinyan Huang; Keith Humphreys; David J Hunter; Anna Jakubowska; Samuel E Jones; Maria Kabisch; David Karasik; Julia A Knight; Ivana Kolcic; Charles Kooperberg; Veli-Matti Kosma; Jennifer Kriebel; Vessela Kristensen; Diether Lambrechts; Claudia Langenberg; Jingmei Li; Xin Li; Sara Lindström; Yongmei Liu; Jian'an Luan; Jan Lubinski; Reedik Mägi; Arto Mannermaa; Judith Manz; Sara Margolin; Jonathan Marten; Nicholas G Martin; Corrado Masciullo; Alfons Meindl; Kyriaki Michailidou; Evelin Mihailov; Lili Milani; Roger L Milne; Martina Müller-Nurasyid; Michael Nalls; Ben M Neale; Heli Nevanlinna; Patrick Neven; Anne B Newman; Børge G Nordestgaard; Janet E Olson; Sandosh Padmanabhan; Paolo Peterlongo; Ulrike Peters; Astrid Petersmann; Julian Peto; Paul D P Pharoah; Nicola N Pirastu; Ailith Pirie; Giorgio Pistis; Ozren Polasek; David Porteous; Bruce M Psaty; Katri Pylkäs; Paolo Radice; Leslie J Raffel; Fernando Rivadeneira; Igor Rudan; Anja Rudolph; Daniela Ruggiero; Cinzia F Sala; Serena Sanna; Elinor J Sawyer; David Schlessinger; Marjanka K Schmidt; Frank Schmidt; Rita K Schmutzler; Minouk J Schoemaker; Robert A Scott; Caroline M Seynaeve; Jacques Simard; Rossella Sorice; Melissa C Southey; Doris Stöckl; Konstantin Strauch; Anthony Swerdlow; Kent D Taylor; Unnur Thorsteinsdottir; Amanda E Toland; Ian Tomlinson; Thérèse Truong; Laufey Tryggvadottir; Stephen T Turner; Diego Vozzi; Qin Wang; Melissa Wellons; Gonneke Willemsen; James F Wilson; Robert Winqvist; Bruce B H R Wolffenbuttel; Alan F Wright; Drakoulis Yannoukakos; Tatijana Zemunik; Wei Zheng; Marek Zygmunt; Sven Bergmann; Dorret I Boomsma; Julie E Buring; Luigi Ferrucci; Grant W Montgomery; Vilmundur Gudnason; Tim D Spector; Cornelia M van Duijn; Behrooz Z Alizadeh; Marina Ciullo; Laura Crisponi; Douglas F Easton; Paolo P Gasparini; Christian Gieger; Tamara B Harris; Caroline Hayward; Sharon L R Kardia; Peter Kraft; Barbara McKnight; Andres Metspalu; Alanna C Morrison; Alex P Reiner; Paul M Ridker; Jerome I Rotter; Daniela Toniolo; André G Uitterlinden; Sheila Ulivi; Henry Völzke; Nicholas J Wareham; David R Weir; Laura M Yerges-Armstrong; Alkes L Price; Kari Stefansson; Jenny A Visser; Ken K Ong; Jenny Chang-Claude; Joanne M Murabito; John R B Perry; Anna Murray Journal: Nat Genet Date: 2015-09-28 Impact factor: 38.330