Evaluation of gametogenic potential of vitrified human umbilical cord Wharton's jelly-derived mesenchymal cells

Cytotherapy. 2014 Feb;16(2):203-12. doi: 10.1016/j.jcyt.2013.10.015.

Abstract

Background aims: Vitrification as an advanced cryopreservation method is recommended for cell storage toward future applications. The purpose of this report was to appraise whether gametogenic potential of these cells is altered by vitrification.

Methods: A two steps method was applied for hUCM cells vitrification. An n-hUCM group of hUCM cells served as control. In order to differentiation of hUCM cells into male germ cells, the cells were induced by retinoic acid, testosterone and testicular-cell-conditioned medium. To evaluate induced hUCM cells toward germ cells, we used immunocytochemistry and karyotyping methods.

Results: v-hUCM cells similar to n-hUCM cells formed flat cells after gametogenic induction, and showed protein expression of germ-cell-specific markers DAZL, VASA (DDX4) and SCP3. Karyotyping pattern remained unchanged in the either groups.

Conclusions: The analysis of these results demonstrates that vitrification does not alter differentiation potential of hUCMs to male germ like cells. These results may set an in vitro pattern to study germ-cell formation from hUCM cells and also as a potential source of sperms for male infertility.

Keywords: gametogenic potential; mesenchymal cells; umbilical cord; vitrification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation
  • Cells, Cultured
  • Culture Media, Conditioned / metabolism
  • Gametogenesis
  • Germ Cells / physiology*
  • Humans
  • Immunohistochemistry
  • Male
  • Mesenchymal Stem Cells / physiology*
  • Testosterone / metabolism
  • Tretinoin / metabolism
  • Umbilical Cord / cytology*
  • Vitrification
  • Wharton Jelly / cytology*

Substances

  • Culture Media, Conditioned
  • Testosterone
  • Tretinoin