Induced Pluripotent Stem Cells from Ovarian Tissue

Curr Protoc Hum Genet. 2017 Oct 18:95:21.10.1-21.10.22. doi: 10.1002/cphg.47.

Abstract

Yamanaka and colleagues revolutionized stem cell biology and regenerative medicine by observing that somatic cells can be reprogrammed into pluripotent stem cells. Evidence indicates that induced pluripotent stem (iPS) cells retain epigenetic memories that bias their spontaneous differentiation into the originating somatic cell type, therefore epigenetic memory may be exploited to improve tissue specific regeneration. We recently showed that iPS cells reprogrammed from ovarian granulosa cells using mouse and human tissue overwhelmingly differentiate homotypically into ovarian steroidogenic and primordial germ cells. Herein we detail a protocol for the culture of human ovarian granulosa cells. We review approaches for reprogramming human ovarian granulosa cells into iPS cells. Standard methods to induce pluripotency are outlined, concentrating on integrative retroviruses. Additionally, alternative protocols for lentivirus and Sendai virus are provided. Each approach has inherent limitations, such as reprogramming efficiency, insertional mutagenesis, and partial reprogramming. Major advances continue to be made in somatic cell reprogramming to identify an optimal approach and utilization in cell-based therapies. © 2017 by John Wiley & Sons, Inc.

Keywords: granulosa cells; homotypic; human ovarian tissue; induced pluripotent stem cells; retrovirus.

Publication types

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

MeSH terms

  • Animals
  • Biomarkers
  • Cell Culture Techniques
  • Cell Line
  • Cell Separation / methods
  • Cell Transformation, Neoplastic
  • Female
  • Genetic Vectors / genetics
  • Granulosa Cells / cytology
  • Humans
  • Immunohistochemistry
  • Induced Pluripotent Stem Cells / cytology*
  • Lentivirus / genetics
  • Ovary / cytology*
  • Phenotype
  • Polymerase Chain Reaction
  • Retroviridae / genetics
  • Sendai virus / genetics
  • Teratoma / etiology
  • Teratoma / pathology
  • Transduction, Genetic

Substances

  • Biomarkers