Login / Signup

Origin, specification and differentiation of a rare supporting-like lineage in the developing mouse gonad.

Chloé MayèreViolaine RegardAitana Perea-GomezCorey BunceYasmine NeirijnckCyril DjariNatividad Bellido-CarrerasPauline SararolsRichard ReevesSimon GreenawayMichelle SimonPam SiggersDiana CondreaFrançoise KühneIvana GantarFurong TangIsabelle StevantLaura BattiNorbert B GhyselinckDagmar WilhelmAndy GreenfieldBlanche CapelMarie-Christine ChaboissierSerge Nef
Published in: Science advances (2022)
Gonadal sex determination represents a unique model for studying cell fate decisions. However, a complete understanding of the different cell lineages forming the developing testis and ovary remains elusive. Here, we investigated the origin, specification, and subsequent sex-specific differentiation of a previously uncharacterized population of supporting-like cells (SLCs) in the developing mouse gonads. The SLC lineage is closely related to the coelomic epithelium and specified as early as E10.5, making it the first somatic lineage to be specified in the bipotential gonad. SLC progenitors are localized within the genital ridge at the interface with the mesonephros and initially coexpress Wnt4 and Sox9 . SLCs become sexually dimorphic around E12.5, progressively acquire a more Sertoli- or pregranulosa-like identity and contribute to the formation of the rete testis and rete ovarii. Last, we found that WNT4 is a crucial regulator of the SLC lineage and is required for normal development of the rete testis.
Keyphrases
  • cell fate
  • stem cells
  • single cell
  • cell proliferation
  • transcription factor
  • cell therapy
  • gene expression
  • mass spectrometry
  • high resolution
  • copy number
  • mesenchymal stem cells