Effects of antioxidants, catalase and α-tocopherol on cell viability and oxidative stress variables in frozen-thawed mice spermatogonial stem cells

Artif Cells Nanomed Biotechnol. 2017 Feb;45(1):63-68. doi: 10.3109/21691401.2016.1138491. Epub 2016 Apr 28.

Abstract

Cryopreservation of spermatogonial stem cells is considered as a useful procedure for preserving fertility in children with testis cancer. SSCs were isolated from testes mice, and then antioxidant was added to the freezing medium. The Bax expression level in antioxidant groups was significantly (P ≤ 0.05) lower than the control group and a significant rise of Bcl2 expression was detected in the antioxidant groups. ROS production with antioxidant was significantly lower compared with the control group. Cryopreservation with the addition of the antioxidants can help increase the number of SSCs and improve the quality and viability of these cells after cryopreservation.

Keywords: Catalase; cryopreservation; spermatogonial stem cell; α-tocopherol.

MeSH terms

  • Adult Germline Stem Cells / cytology
  • Adult Germline Stem Cells / metabolism*
  • Animals
  • Antioxidants / pharmacology*
  • Catalase / pharmacology*
  • Cell Survival / drug effects
  • Cells, Cultured
  • Cryopreservation*
  • Freezing
  • Male
  • Mice
  • Oxidative Stress / drug effects*
  • alpha-Tocopherol / pharmacology*

Substances

  • Antioxidants
  • Catalase
  • alpha-Tocopherol