Single-cell roadmap of human gonadal development.
Luz Garcia-AlonsoValentina LorenziCecilia Icoresi MazzeoJoão Pedro Alves-LopesKenny RobertsCarmen Sancho-SerraJustin EngelbertMagda MarečkováWolfram H GruhnRachel Anne BottingTong LiBerta CrespoStijn van DongenVladimir Yu KiselevElena PrigmoreMary HerbertAshley MoffettAlain ChédotalOmer Ali BayraktarAzim SuraniMuzlifah HaniffaRoser Vento-TormoPublished in: Nature (2022)
Gonadal development is a complex process that involves sex determination followed by divergent maturation into either testes or ovaries 1 . 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.
Keyphrases
- single cell
- endothelial cells
- induced pluripotent stem cells
- pluripotent stem cells
- rna seq
- induced apoptosis
- high throughput
- transcription factor
- metabolic syndrome
- mesenchymal stem cells
- single molecule
- pregnant women
- oxidative stress
- skeletal muscle
- adipose tissue
- mass spectrometry
- cell proliferation
- cell therapy
- high fat diet induced
- dna methylation
- preterm birth
- cell death
- endoplasmic reticulum stress
- pregnancy outcomes
- living cells