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Gonadotrophs have a dual origin, with most derived from early postnatal pituitary stem cells

Author

Listed:
  • Daniel Sheridan

    (The Francis Crick Institute)

  • Probir Chakravarty

    (The Francis Crick Institute)

  • Gil Golan

    (Technion Israel Institute of Technology)

  • Yiolanda Shiakola

    (The Francis Crick Institute)

  • Jessica Olsen

    (The Francis Crick Institute)

  • Elise Burnett

    (The Francis Crick Institute)

  • Christophe Galichet

    (The Francis Crick Institute)

  • Tatiana Fiordelisio

    (Universidad Nacional Autonoma de Mexico)

  • Patrice Mollard

    (Inserm)

  • Philippa Melamed

    (Technion Israel Institute of Technology)

  • Robin Lovell-Badge

    (The Francis Crick Institute)

  • Karine Rizzoti

    (The Francis Crick Institute)

Abstract

Gonadotrophs are the essential pituitary endocrine cells for reproduction. They produce both luteinizing (LH) and follicle-stimulating (FSH) hormones that act on the gonads to promote germ cell maturation and steroidogenesis. Their secretion is controlled by the hypothalamic gonadotrophin-releasing hormone (GnRH), and gonadal steroid feedback. Gonadotrophs first appear in the embryonic pituitary, along with other endocrine cell types, and all expand after birth. While gonadotrophs may display heterogeneity in their response to GnRH, they appear, at least transcriptionally, as a homogenous population. The pituitary also contains a population of stem cells (SCs), whose contribution to postnatal growth is unclear, in part because endocrine cells maintain the ability to proliferate. Here we show an unsuspected dual origin of the murine adult gonadotroph population, with most gonadotrophs originating from postnatal pituitary stem cells starting early postnatally and up to puberty, while embryonic gonadotrophs are maintained. We further demonstrate that postnatal gonadotroph differentiation happens independently of gonadal signals and is not affected by impairment of GnRH signalling. The division of gonadotrophs based on separate origins has implications for our understanding of the establishment and regulation of reproductive functions, both in health and in disease.

Suggested Citation

  • Daniel Sheridan & Probir Chakravarty & Gil Golan & Yiolanda Shiakola & Jessica Olsen & Elise Burnett & Christophe Galichet & Tatiana Fiordelisio & Patrice Mollard & Philippa Melamed & Robin Lovell-Bad, 2025. "Gonadotrophs have a dual origin, with most derived from early postnatal pituitary stem cells," Nature Communications, Nature, vol. 16(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59495-7
    DOI: 10.1038/s41467-025-59495-7
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    References listed on IDEAS

    as
    1. Shu Zhang & Yueli Cui & Xinyi Ma & Jun Yong & Liying Yan & Ming Yang & Jie Ren & Fuchou Tang & Lu Wen & Jie Qiao, 2020. "Single-cell transcriptomics identifies divergent developmental lineage trajectories during human pituitary development," Nature Communications, Nature, vol. 11(1), pages 1-16, December.
    2. H. James McQuillan & Jenny Clarkson & Alexia Kauff & Su Young Han & Siew Hoong Yip & Isaiah Cheong & Robert Porteous & Alison K. Heather & Allan E. Herbison, 2022. "Definition of the estrogen negative feedback pathway controlling the GnRH pulse generator in female mice," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    3. Konstantin Khetchoumian & Aurélio Balsalobre & Alexandre Mayran & Helen Christian & Valérie Chénard & Julie St-Pierre & Jacques Drouin, 2019. "Pituitary cell translation and secretory capacities are enhanced cell autonomously by the transcription factor Creb3l2," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
    4. Frederique Ruf-Zamojski & Zidong Zhang & Michel Zamojski & Gregory R. Smith & Natalia Mendelev & Hanqing Liu & German Nudelman & Mika Moriwaki & Hanna Pincas & Rosa Gomez Castanon & Venugopalan D. Nai, 2021. "Single nucleus multi-omics regulatory landscape of the murine pituitary," Nature Communications, Nature, vol. 12(1), pages 1-20, December.
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