Histological chorioamnionitis in preterm prelabor rupture of the membranes is associated with increased expression of galectin-3 by amniotic epithelium

J Matern Fetal Neonatal Med. 2017 Sep;30(18):2232-2236. doi: 10.1080/14767058.2016.1243100. Epub 2016 Oct 25.

Abstract

Purpose: Gal-3, which can regulate immune responses upon infection and inflammation, was not studied so far in intrauterine infection leading to preterm prelabor rupture of the membranes (PPROM), although gal-1 was reported to be implicated in the process. Gal-3 mRNA and protein expression in amnion and its changes during histological chorioamnionitis were studied here.

Materials and methods: Fetal membranes were obtained from women with PPROM with (n =15) and without histological chorioamnionitis (n =15) during second and third trimester. Immunohistochemical reactivity was evaluated semiquantitatively and analyzed using t-test. Galectin profile of amniotic epithelia was determined by polymerase chain reaction (PCR) and change assessed in gal-3 in PPROM with (n =5) or without histological chorioamnionitis (n =5) by real-time PCR.

Results: Human amniotic epithelium was found to express gal-1, gal-3, gal-7 and gal-8 mRNA. Gal-3 mRNA and protein is increased in fetal membranes and in the amniotic epithelium in patients with chorionamnionitis.

Conclusion: Histological chorioamnionitis is associated with increased gal-3 expression and strong immunoreactivity of the amnion. Gal-3 may participate in the regulation of the inflammatory responses to chorioamniotic infection and/or direct interaction with pathogens.

Keywords: Chorioamnion; fetal membranes; galectin; inflammation; prelabor; preterm delivery; rupture of membranes.

MeSH terms

  • Amnion / metabolism*
  • Amnion / pathology
  • Blood Proteins
  • Case-Control Studies
  • Chorioamnionitis / genetics
  • Chorioamnionitis / metabolism
  • Chorioamnionitis / pathology*
  • Female
  • Fetal Membranes, Premature Rupture / genetics
  • Fetal Membranes, Premature Rupture / metabolism*
  • Galectin 3 / biosynthesis*
  • Galectins / biosynthesis
  • Humans
  • Obstetric Labor, Premature / metabolism
  • Pregnancy
  • RNA, Messenger / metabolism
  • Real-Time Polymerase Chain Reaction

Substances

  • Blood Proteins
  • Galectin 3
  • Galectins
  • LGALS3 protein, human
  • LGALS8 protein, human
  • RNA, Messenger