Effects of upregulation of Hsp27 expression on oocyte development and maturation derived from polycystic ovary syndrome

PLoS One. 2013 Dec 31;8(12):e83402. doi: 10.1371/journal.pone.0083402. eCollection 2013.

Abstract

Heat shock protein 27 (Hsp27) is a heat shock protein family member which can inhibit apoptosis. Our previous studies reported down-regulated Hsp27 in ovarian tissue derived from women with polycystic ovary syndrome (PCOS) however, the exact effect of Hsp27 on oocyte maturation and developmental competence in PCOS is unclear. The effect of Hsp27 over-expression was studied in vitro using oocytes derived from PCOS patients. An artificial GFP-plasmid was injected into human oocyte to increase Hsp27 protein level. Oocyte maturation was evaluated by morphological observation. Mature oocytes were fertilized by intracytoplasmic sperm injection (ICSI) and embryonic developmental competence was evaluated. Critical apoptotic factors and cytokines were measured at both the mRNA and protein level. Our results revealed that Overexpression of HSP27 lowered the maturation rate of oocytes derived from PCOS patients. Meanwhile, fertilization rate and high quality embryo rate were similar between the Hsp27 overexpressing group and controls; however, the blastocyst formation rate in this group was significantly higher than control. Expression analysis revealed that the oocyte-secreted factors, BMP15 and GDF9, and the apoptotic-related regulators, Caspase 3, 8 and 9, were all significantly decreased in Hsp27 overexpressing oocytes. In conclusion, upregulation of Hsp27 inhibits oocyte maturation from PCOS patients, but improves embryonic developmental potential.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis / genetics
  • Caspases / genetics
  • Caspases / metabolism
  • Cytokines / genetics
  • Cytokines / metabolism
  • Embryonic Development / genetics
  • Female
  • Genetic Vectors
  • HSP27 Heat-Shock Proteins / genetics*
  • HSP27 Heat-Shock Proteins / metabolism*
  • Heat-Shock Proteins
  • Humans
  • In Vitro Techniques
  • Molecular Chaperones
  • Oocytes / growth & development
  • Oocytes / metabolism*
  • Oocytes / pathology*
  • Oogenesis / genetics
  • Polycystic Ovary Syndrome / genetics*
  • Polycystic Ovary Syndrome / metabolism
  • Polycystic Ovary Syndrome / pathology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Sperm Injections, Intracytoplasmic
  • Up-Regulation

Substances

  • Cytokines
  • HSP27 Heat-Shock Proteins
  • HSPB1 protein, human
  • Heat-Shock Proteins
  • Molecular Chaperones
  • RNA, Messenger
  • Caspases

Grants and funding

This work was supported by grants from the National Natural Projects of China (30800394 and 81070465) and 973 Program (2012CB944703 and 2012CB944902). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.