Effect of 2-deoxyglucose-mediated inhibition of glycolysis on migration and invasion of HTR-8/SVneo trophoblast cells

J Reprod Immunol. 2023 Sep:159:104123. doi: 10.1016/j.jri.2023.104123. Epub 2023 Jul 20.

Abstract

The proper invasion of trophoblasts is crucial for embryo implantation and placental development, which is helpful to establish a correct maternal-fetal relationship. Trophoblasts can produce a large amount of lactate through aerobic glycolysis during early pregnancy. Lactate creates a low pH microenvironment around the embryo to help uterine tissue decompose and promote the invasion of trophoblasts. The purpose of this study is to reveal the the potential mechanism of aerobic glycolysis regulating the invasiveness of trophoblasts by investigating the effect of 2-Deoxy-D-glucose (2-DG), a glycolysis inhibitor, on the biological function of HTR-8/SVneo trophoblast cells, the expressions of epithelial mesenchymal transformation (EMT) markers and invasion-related factors. 2-DG could inhibit the aerobic glycolysis of trophoblasts and decrease the activity of trophoblasts in a dose-dependent manner. Moreover, 2-DG inhibited the EMT of HTR-8/SVneo cells, down-regulated the expression of invasion-related factors matrix metalloproteinase 2/9 (MMP2/9) and up-regulated the expression of tissue inhibitor of matrix metalloproteinases 1/2 (TIMP1/2), thus inhibiting cell migration and invasion. This paper provides a foundation in the significance of aerobic glycolysis of trophoblasts in the process of invasion, and also provides ideas and insights for the promotion of embryo implantation.

Keywords: 2-deoxyglucose; Epithelial-mesenchymal transition (EMT); Glycolysis; Invasion; Trophoblasts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Cell Movement
  • Deoxyglucose / metabolism
  • Deoxyglucose / pharmacology
  • Female
  • Humans
  • Lactates / metabolism
  • Lactates / pharmacology
  • Matrix Metalloproteinase 2 / metabolism
  • Placenta* / metabolism
  • Pregnancy
  • Signal Transduction
  • Trophoblasts* / metabolism

Substances

  • Matrix Metalloproteinase 2
  • Deoxyglucose
  • Lactates