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Single-cell roadmap of human gonadal development

Author

Listed:
  • Luz Garcia-Alonso

    (Wellcome Sanger Institute)

  • Valentina Lorenzi

    (Wellcome Sanger Institute)

  • Cecilia Icoresi Mazzeo

    (Wellcome Sanger Institute)

  • João Pedro Alves-Lopes

    (University of Cambridge
    University of Cambridge)

  • Kenny Roberts

    (Wellcome Sanger Institute)

  • Carmen Sancho-Serra

    (Wellcome Sanger Institute)

  • Justin Engelbert

    (Newcastle University)

  • Magda Marečková

    (Wellcome Sanger Institute
    University of Oxford)

  • Wolfram H. Gruhn

    (University of Cambridge
    University of Cambridge)

  • Rachel A. Botting

    (Newcastle University)

  • Tong Li

    (Wellcome Sanger Institute)

  • Berta Crespo

    (University College London)

  • Stijn Dongen

    (Wellcome Sanger Institute)

  • Vladimir Yu Kiselev

    (Wellcome Sanger Institute)

  • Elena Prigmore

    (Wellcome Sanger Institute)

  • Mary Herbert

    (Newcastle University)

  • Ashley Moffett

    (University of Cambridge)

  • Alain Chédotal

    (Sorbonne Université, INSERM, CNRS, Institut de la Vision)

  • Omer Ali Bayraktar

    (Wellcome Sanger Institute)

  • Azim Surani

    (University of Cambridge
    University of Cambridge
    Jeffrey Cheah Biomedical Centre)

  • Muzlifah Haniffa

    (Wellcome Sanger Institute
    Newcastle University)

  • Roser Vento-Tormo

    (Wellcome Sanger Institute)

Abstract

Gonadal development is a complex process that involves sex determination followed by divergent maturation into either testes or ovaries1. Historically, limited tissue accessibility, a lack of reliable in vitro models and critical differences between humans and mice have hampered our knowledge of human gonadogenesis, despite its importance in gonadal conditions and infertility. Here, we generated a comprehensive map of first- and second-trimester human gonads using a combination of single-cell and spatial transcriptomics, chromatin accessibility assays and fluorescent microscopy. We extracted human-specific regulatory programmes that control the development of germline and somatic cell lineages by profiling equivalent developmental stages in mice. In both species, we define the somatic cell states present at the time of sex specification, including the bipotent early supporting population that, in males, upregulates the testis-determining factor SRY and sPAX8s, a gonadal lineage located at the gonadal–mesonephric interface. In females, we resolve the cellular and molecular events that give rise to the first and second waves of granulosa cells that compartmentalize the developing ovary to modulate germ cell differentiation. In males, we identify human SIGLEC15+ and TREM2+ fetal testicular macrophages, which signal to somatic cells outside and inside the developing testis cords, respectively. This study provides a comprehensive spatiotemporal map of human and mouse gonadal differentiation, which can guide in vitro gonadogenesis.

Suggested Citation

  • Luz Garcia-Alonso & Valentina Lorenzi & Cecilia Icoresi Mazzeo & João Pedro Alves-Lopes & Kenny Roberts & Carmen Sancho-Serra & Justin Engelbert & Magda Marečková & Wolfram H. Gruhn & Rachel A. Bottin, 2022. "Single-cell roadmap of human gonadal development," Nature, Nature, vol. 607(7919), pages 540-547, July.
  • Handle: RePEc:nat:nature:v:607:y:2022:i:7919:d:10.1038_s41586-022-04918-4
    DOI: 10.1038/s41586-022-04918-4
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    Cited by:

    1. Denis Houzelstein & Caroline Eozenou & Carlos F. Lagos & Maëva Elzaiat & Joelle Bignon-Topalovic & Inma Gonzalez & Vincent Laville & Laurène Schlick & Somboon Wankanit & Prochi Madon & Jyotsna Kirtane, 2024. "A conserved NR5A1-responsive enhancer regulates SRY in testis-determination," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    2. Chao-Hui Chang & Feng Liu & Stefania Militi & Svenja Hester & Reshma Nibhani & Siwei Deng & James Dunford & Aniko Rendek & Zahir Soonawalla & Roman Fischer & Udo Oppermann & Siim Pauklin, 2024. "The pRb/RBL2-E2F1/4-GCN5 axis regulates cancer stem cell formation and G0 phase entry/exit by paracrine mechanisms," Nature Communications, Nature, vol. 15(1), pages 1-29, December.

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