Oxygen-regulated gene expression in murine cumulus cells

Reprod Fertil Dev. 2015 Jan;27(2):407-18. doi: 10.1071/RD13249.

Abstract

Oxygen is an important component of the environment of the cumulus-oocyte complex (COC), both in vivo within the ovarian follicle and during in vitro oocyte maturation (IVM). Cumulus cells have a key role in supporting oocyte development, and cumulus cell function and gene expression are known to be altered when the environment of the COC is perturbed. Oxygen-regulated gene expression is mediated through the actions of the transcription factors, the hypoxia-inducible factors (HIFs). In the present study, the effect of oxygen on cumulus cell gene expression was examined following in vitro maturation of the murine COC at 2%, 5% or 20% oxygen. Increased expression of HIF-responsive genes, including glucose transporter-1, lactate dehydrogenase A and BCL2/adenovirus E1B interacting protein 3, was observed in cumulus cells matured at 2% or 5%, compared with 20% oxygen. Stabilisation of HIF1α protein in cumulus cells exposed to low oxygen was confirmed by western blot and HIF-mediated transcriptional activity was demonstrated using a transgenic mouse expressing green fluorescent protein under the control of a promoter containing hypoxia response elements. These results indicate that oxygen concentration influences cumulus cell gene expression and support a role for HIF1α in mediating the cumulus cell response to varying oxygen.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenovirus E1B Proteins / metabolism
  • Analysis of Variance
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Blotting, Western
  • Cumulus Cells / metabolism*
  • DNA Primers / genetics
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation, Developmental / drug effects*
  • Gene Expression Regulation, Developmental / physiology
  • Glucose Transporter Type 1 / metabolism
  • Green Fluorescent Proteins / metabolism
  • In Vitro Oocyte Maturation Techniques / methods*
  • Isoenzymes / metabolism
  • L-Lactate Dehydrogenase / metabolism
  • Lactate Dehydrogenase 5
  • Mice
  • Mice, Transgenic
  • Oxygen / pharmacology*

Substances

  • Adenovirus E1B Proteins
  • Basic Helix-Loop-Helix Transcription Factors
  • DNA Primers
  • Glucose Transporter Type 1
  • Isoenzymes
  • Green Fluorescent Proteins
  • L-Lactate Dehydrogenase
  • Lactate Dehydrogenase 5
  • Oxygen