Login / Signup

X‑chromosome loss rescues Sertoli cell maturation and spermatogenesis in Klinefelter syndrome.

Sofia Boeg WingeNiels E SkakkebaekLise AksglaedeGülizar SaritaşEwa Rajpert-De MeytsEllen GoossensAnders JuulKristian Almstrup
Published in: Cell death & disease (2024)
Klinefelter syndrome (47,XXY) causes infertility with a testicular histology comprising two types of Sertoli cell-only tubules, representing mature and immature-like Sertoli cells, and occasionally focal spermatogenesis. Here, we show that the immature-like Sertoli cells highly expressed XIST and had two X-chromosomes, while the mature Sertoli cells lacked XIST expression and had only one X-chromosome. Sertoli cells supporting focal spermatogenesis also lacked XIST expression and the additional X-chromosome, while the spermatogonia expressed XIST despite having only one X-chromosome. XIST was expressed in Sertoli cells until puberty, where a gradual loss was observed. Our results suggest that a micro-mosaic loss of the additional X-chromosome is needed for Sertoli cells to mature and to allow focal spermatogenesis.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • endoplasmic reticulum stress
  • stem cells
  • copy number
  • signaling pathway
  • oxidative stress
  • single cell
  • skeletal muscle
  • genome wide