Functional Oocytes Derived from Granulosa Cells

Cell Rep. 2019 Dec 24;29(13):4256-4267.e9. doi: 10.1016/j.celrep.2019.11.080.

Abstract

The generation of genomically stable and functional oocytes has great potential for preserving fertility and restoring ovarian function. It remains elusive whether functional oocytes can be generated from adult female somatic cells through reprogramming to germline-competent pluripotent stem cells (gPSCs) by chemical treatment alone. Here, we show that somatic granulosa cells isolated from adult mouse ovaries can be robustly induced to generate gPSCs by a purely chemical approach, with additional Rock inhibition and critical reprogramming facilitated by crotonic sodium or acid. These gPSCs acquired high germline competency and could consistently be directed to differentiate into primordial-germ-cell-like cells and form functional oocytes that produce fertile mice. Moreover, gPSCs promoted by crotonylation and the derived germ cells exhibited longer telomeres and high genomic stability like PGCs in vivo, providing additional evidence supporting the safety and effectiveness of chemical induction, which is particularly important for germ cells in genetic inheritance.

Keywords: chemical reprogramming; granulosa cell; oocyte; pluripotent stem cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Female
  • Fertility / drug effects
  • Genomic Instability / drug effects
  • Germ Cells / cytology
  • Granulosa Cells / cytology*
  • Granulosa Cells / drug effects
  • Granulosa Cells / metabolism
  • Humans
  • Induced Pluripotent Stem Cells / cytology
  • Induced Pluripotent Stem Cells / drug effects
  • Induced Pluripotent Stem Cells / metabolism
  • Meiosis / drug effects
  • Mice, Inbred BALB C
  • Oocytes / cytology*
  • Oocytes / drug effects
  • Oocytes / metabolism
  • Organogenesis / drug effects
  • Protein Kinase Inhibitors / pharmacology
  • Telomere / metabolism
  • rho-Associated Kinases / antagonists & inhibitors
  • rho-Associated Kinases / metabolism

Substances

  • Protein Kinase Inhibitors
  • rho-Associated Kinases