Interleukin-6 enhances porcine parthenote development in vitro, through the IL-6/Stat3 signaling pathway

J Reprod Dev. 2012;58(4):453-60. doi: 10.1262/jrd.2012-015. Epub 2012 Apr 21.

Abstract

Signal transducer and activator of transcription-3 (Stat3) plays a central role in interleukin-6 (IL-6)-mediated cell proliferation by inhibiting apoptosis in a variety of cell types. The Stat3 pathway is essential for embryonic development. The aim of this study was to determine the effects of recombinant IL-6 on the viability and development of porcine diploid parthenotes cultured in vitro. Four-cell parthenotes, derived in vitro, were cultured to the blastocyst stage, with or without recombinant IL-6. The addition of 10 or 100 ng/ml of recombinant swine IL-6 into PZM3 medium increased the development rate of parthenotes to the blastocyst stage (P<0.05). When supplemented with 10 ng/ml of recombinant swine IL-6, the number of parthenotes at the blastocyst stage increased (P<0.05) and apoptosis decreased (P<0.05). Real-time RT-PCR experiments revealed that the addition of recombinant swine IL-6 decreased the mRNA expression of the pro-apoptotic gene Caspase3 (P<0.01) but increased the expression levels of the anti-apoptotic genes Bcl2l1 and Survivin. IL-6 receptors and Stat3 mRNA expression were upregulated after treatment with 10 ng/ml recombinant swine IL-6. Immunoblots and fluorescence labeling experiments showed that the levels of phosphorylated Stat3 were upregulated. These results suggest that recombinant swine IL-6 prevents apoptosis of porcine parthenotes and enhances porcine embryo viability through the IL-6/Stat3 signaling pathway in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Apoptosis Regulatory Proteins / genetics
  • Apoptosis Regulatory Proteins / metabolism
  • Blastocyst / physiology*
  • Cumulus Cells / physiology
  • Ectogenesis*
  • Female
  • Gene Expression Regulation, Developmental
  • In Vitro Oocyte Maturation Techniques
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism*
  • Oocytes / physiology*
  • Parthenogenesis
  • Phosphorylation
  • Protein Processing, Post-Translational
  • RNA, Messenger / metabolism
  • Receptors, Interleukin-6 / genetics
  • Receptors, Interleukin-6 / metabolism*
  • Recombinant Proteins / metabolism
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism*
  • Signal Transduction*
  • Sus scrofa

Substances

  • Apoptosis Regulatory Proteins
  • Interleukin-6
  • RNA, Messenger
  • Receptors, Interleukin-6
  • Recombinant Proteins
  • STAT3 Transcription Factor