Potential role for nectin-4 in the pathogenesis of pre-eclampsia: a molecular genetic study

BMC Med Genet. 2018 Sep 14;19(1):166. doi: 10.1186/s12881-018-0681-y.

Abstract

Background: Nectins are cell adhesion molecules that play a pivotal role in adherens junctions and tight junctions. Our previous study using whole-genome oligonucleotide microarrays revealed that nectin-4 was upregulated in pre-eclamptic placentas. We investigated the role of nectin-4 in the etiology of pre-eclampsia.

Methods: We investigated the expression of nectin-4 using real-time RT-PCR, western blot and immunostaining. Additionally, we performed matrigel invasion assay and cytotoxicity assay using cells overexpressing the nectin-4.

Results: NECTIN4 transcripts were elevated in pre-eclamptic placentas relative to uncomplicated pregnancies. Nectin-4 protein levels in pre-eclamptic placentas were higher on a semi-quantitative western blot. Nectin-4 was localized at the apical cell membrane in syncytiotrophoblast cells and not at the adherens junctions. Nectin-4 was also detected in cytotrophoblasts and a subset of cells in the decidua. Nectin-4 overexpressing trophoblast cells migrated normally in the matrix. However, Natural killer (NK) cells showed a strong cytotoxic effect against nectin-4 overexpressing trophoblast cells. No causative genetic variation was evident in the NECTIN4 gene from a pre-eclamptic placenta.

Conclusions: There are as yet unknown factors that induce nectin-4 overexpression in trophoblast cells that may contribute to abnormal placentation via an aberrant immune response and the onset of a pre-eclamptic pregnancy.

Keywords: Nectin-4; Pre-eclampsia; Trophoblast.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Case-Control Studies
  • Cell Adhesion Molecules / genetics*
  • Cell Adhesion Molecules / immunology
  • Cesarean Section
  • Cytotoxicity, Immunologic
  • Decidua / immunology*
  • Decidua / pathology
  • Female
  • Gene Expression Regulation
  • Humans
  • Immunity, Innate
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / pathology
  • Pre-Eclampsia / genetics*
  • Pre-Eclampsia / immunology
  • Pre-Eclampsia / pathology
  • Pre-Eclampsia / surgery
  • Pregnancy
  • RNA, Messenger / genetics*
  • RNA, Messenger / immunology
  • Trophoblasts / immunology*
  • Trophoblasts / pathology

Substances

  • Cell Adhesion Molecules
  • RNA, Messenger
  • NECTIN4 protein, human