Homeobox gene Distal-less 3 is a regulator of villous cytotrophoblast differentiation and its expression is increased in human idiopathic foetal growth restriction

J Mol Med (Berl). 2012 Mar;90(3):273-84. doi: 10.1007/s00109-011-0836-1. Epub 2011 Nov 24.

Abstract

Human idiopathic foetal growth restriction (FGR) is frequently associated with placental insufficiency. In our previous studies, we have reported the isolation and characterisation of the homeobox gene Distal-less 3 (DLX3) in the human placenta. In this study, we have investigated the level of DLX3 expression in idiopathic FGR-affected placentae and determined its functional role in villous trophoblast differentiation. FGR-affected placentae (n = 25) were collected based on well-defined clinical criteria and matched for gestation with control uncomplicated pregnancies (n = 25). Real-time polymerase chain reaction and immunoblotting showed increased DLX3 mRNA and protein expression in FGR-affected placentae compared with gestation-matched controls. Qualitative immunohistochemistry revealed DLX3 localisation in the syncytiotrophoblast, cytotrophoblasts and endothelial cells surrounding the foetal capillaries in both FGR-affected and control placentae. Down-regulation of DLX3 in primary villous trophoblast cells and a trophoblast-derived cell line showed decreased expression of differentiation markers, 3βHSD, βhCG and syncytin. Therefore, we conclude that increased DLX3 expression in FGR may contribute to trophoblast dysfunction observed in FGR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Cell Differentiation*
  • Cell Line
  • Cells, Cultured
  • Female
  • Fetal Growth Retardation / metabolism
  • Fetal Growth Retardation / physiopathology*
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism*
  • Humans
  • Placenta / metabolism
  • Placental Insufficiency / genetics
  • Placental Insufficiency / metabolism
  • Placental Insufficiency / physiopathology
  • Pregnancy
  • Pregnancy Complications / genetics
  • Pregnancy Complications / metabolism
  • Pregnancy Trimester, Third
  • RNA, Messenger
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Trophoblasts / cytology*
  • Up-Regulation*

Substances

  • Distal-less homeobox proteins
  • Homeodomain Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • Transcription Factors