Decoding the pathogenesis of spermatogenic failure in cryptorchidism through single-cell transcriptomic profiling

Cell Rep Med. 2024 Sep 17;5(9):101709. doi: 10.1016/j.xcrm.2024.101709. Epub 2024 Sep 2.

Abstract

Cryptorchidism, commonly known as undescended testis, affects 1%-9% of male newborns, posing infertility and testis tumor risks. Despite its prevalence, the detailed pathophysiology underlying male infertility within cryptorchidism remains unclear. Here, we profile and analyze 46,644 single-cell transcriptomes from individual testicular cells obtained from adult males diagnosed with cryptorchidism and healthy controls. Spermatogenesis compromise in cryptorchidism links primarily to spermatogonium self-renewal and differentiation dysfunctions. We illuminate the involvement of testicular somatic cells, including immune cells, thereby unveiling the activation and degranulation of mast cells in cryptorchidism. Mast cells are identified as contributors to interstitial fibrosis via transforming growth factor β1 (TGF-β1) and cathepsin G secretion. Furthermore, significantly increased levels of secretory proteins indicate mast cell activation and testicular fibrosis in the seminal plasma of individuals with cryptorchidism compared to controls. These insights serve as valuable translational references, enriching our comprehension of testicular pathogenesis and informing more precise diagnosis and targeted therapeutic strategies for cryptorchidism.

Keywords: cryptorchidism; male infertility; spermatogonial stem cells; testicular interstitial fibrosis.

MeSH terms

  • Adult
  • Cryptorchidism* / genetics
  • Cryptorchidism* / metabolism
  • Cryptorchidism* / pathology
  • Fibrosis
  • Gene Expression Profiling*
  • Humans
  • Infertility, Male / genetics
  • Infertility, Male / pathology
  • Male
  • Mast Cells / metabolism
  • Mast Cells / pathology
  • Single-Cell Analysis* / methods
  • Spermatogenesis* / genetics
  • Spermatogonia / metabolism
  • Spermatogonia / pathology
  • Testis / metabolism
  • Testis / pathology
  • Transcriptome* / genetics
  • Transforming Growth Factor beta1 / genetics
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Transforming Growth Factor beta1