Stage-specific integration of maternal and embryonic peroxisome proliferator-activated receptor delta signaling is critical to pregnancy success

J Biol Chem. 2007 Dec 28;282(52):37770-82. doi: 10.1074/jbc.M706577200. Epub 2007 Oct 26.

Abstract

Successful pregnancy depends on well coordinated developmental events involving both maternal and embryonic components. Although a host of signaling pathways participate in implantation, decidualization, and placentation, whether there is a common molecular link that coordinates these processes remains unknown. By exploiting genetic, molecular, pharmacological, and physiological approaches, we show here that the nuclear transcription factor peroxisome proliferator-activated receptor (PPAR) delta plays a central role at various stages of pregnancy, whereas maternal PPARdelta is critical to implantation and decidualization, and embryonic PPARdelta is vital for placentation. Using trophoblast stem cells, we further elucidate that a reciprocal relationship between PPARdelta-AKT and leukemia inhibitory factor-STAT3 signaling pathways serves as a cell lineage sensor to direct trophoblast cell fates during placentation. This novel finding of stage-specific integration of maternal and embryonic PPARdelta signaling provides evidence that PPARdelta is a molecular link that coordinates implantation, decidualization, and placentation crucial to pregnancy success. This study is clinically relevant because deferral of on time implantation leads to spontaneous pregnancy loss, and defective trophoblast invasion is one cause of preeclampsia in humans.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Decidua / metabolism
  • Embryo Implantation
  • Female
  • Fertilization
  • Gene Expression Regulation, Developmental*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Ovulation
  • PPAR delta / metabolism*
  • Placenta / metabolism
  • Pregnancy
  • Pregnancy, Animal / physiology*
  • STAT3 Transcription Factor / physiology
  • Signal Transduction
  • Stem Cells / cytology
  • Time Factors
  • Trophoblasts / metabolism

Substances

  • PPAR delta
  • STAT3 Transcription Factor
  • Stat3 protein, mouse