Chorioamnionitis and increased galectin-1 expression in PPROM --an anti-inflammatory response in the fetal membranes?

Am J Reprod Immunol. 2008 Oct;60(4):298-311. doi: 10.1111/j.1600-0897.2008.00624.x.

Abstract

Problem: Galectin-1 can regulate immune responses upon infection and inflammation. We determined galectin-1 expression in the chorioamniotic membranes and its changes during histological chorioamnionitis.

Method of study: Chorioamniotic membranes were obtained from women with normal pregnancy (n = 5) and from patients with pre-term pre-labor rupture of the membranes (PPROM) with (n = 8) and without histological chorioamnionitis (n = 8). Galectin-1 mRNA and protein were localized by in situ hybridization and immunohistochemistry. Galectin-1 mRNA expression was also determined by quantitative reverse transcriptase polymerase chain reaction.

Results: Galectin-1 mRNA and protein were detected in the amniotic epithelium, chorioamniotic fibroblasts/myofibroblasts and macrophages, chorionic trophoblasts, and decidual stromal cells. In patients with PPROM, galectin-1 mRNA expression in the fetal membranes was higher (2.07-fold, P = 0.002) in those with chorioamnionitis than in those without. Moreover, chorioamionitis was associated with a strong galectin-1 immunostaining in amniotic epithelium, chorioamniotic mesodermal cells, and apoptotic bodies.

Conclusion: Chorioamnionitis is associated with an increased galectin-1 mRNA expression and strong immunoreactivity of the chorioamniotic membranes; thus, galectin-1 may be involved in the regulation of the inflammatory responses to chorioamniotic infection.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Chorioamnionitis / immunology
  • Chorioamnionitis / metabolism*
  • Chorioamnionitis / pathology
  • Cross-Sectional Studies
  • Extraembryonic Membranes / immunology
  • Extraembryonic Membranes / metabolism*
  • Extraembryonic Membranes / pathology
  • Female
  • Fetal Membranes, Premature Rupture / immunology
  • Fetal Membranes, Premature Rupture / metabolism
  • Fetal Membranes, Premature Rupture / pathology
  • Galectin 1 / biosynthesis*
  • Humans
  • Pregnancy
  • RNA, Messenger / metabolism

Substances

  • Galectin 1
  • RNA, Messenger