Regulation of meiotic progression by Sertoli-cell androgen signaling

Mol Biol Cell. 2020 Dec 1;31(25):2841-2862. doi: 10.1091/mbc.E20-05-0334. Epub 2020 Oct 7.

Abstract

Androgen receptor (AR) signaling in Sertoli cells is known to be important for germ-cell progression through meiosis, but the extent to which androgens indirectly regulate specific meiotic stages is not known. Here, we combine synchronization of spermatogenesis, cytological analyses and single-cell RNAseq (scRNAseq) in the Sertoli-cell androgen receptor knockout (SCARKO) mutant and control mice, and demonstrate that SCARKO mutant spermatocytes exhibited normal expression and localization of key protein markers of meiotic prophase events, indicating that initiation of meiotic prophase is not androgen dependent. However, spermatocytes from SCARKO testes failed to acquire competence for the meiotic division phase. ScRNAseq analysis of wild-type and SCARKO mutant testes revealed a molecular transcriptomic block in an early meiotic prophase state (leptotene/zygotene) in mutant germ cells, and identified several misregulated genes in SCARKO Sertoli cells, many of which have been previously implicated in male infertility. Together, our coordinated cytological and scRNAseq analyses identified germ-cell intrinsic and extrinsic genes responsive to Sertoli-cell androgen signaling that promotes cellular states permissive for the meiotic division phase.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androgens / metabolism*
  • Androgens / physiology
  • Animals
  • Male
  • Meiosis / physiology*
  • Meiotic Prophase I
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Prophase
  • Receptors, Androgen / metabolism*
  • Receptors, Androgen / physiology
  • Sequence Analysis, RNA / methods
  • Sertoli Cells / metabolism*
  • Sertoli Cells / physiology
  • Signal Transduction
  • Single-Cell Analysis / methods
  • Spermatocytes / metabolism
  • Spermatogenesis / physiology
  • Testis / metabolism

Substances

  • Androgens
  • Receptors, Androgen