Simulated ischaemia/reperfusion impairs trophoblast function through divergent oxidative stress- and MMP-9-dependent mechanisms

Biosci Rep. 2024 Nov 27;44(11):BSR20240763. doi: 10.1042/BSR20240763.

Abstract

Early-onset pre-eclampsia is believed to arise from defective placentation in the first trimester, leading to placental ischaemia/reperfusion (I/R) and oxidative stress. However, our current understanding of the effects of I/R and oxidative stress on trophoblast function is ambiguous in part due to studies exposing trophoblasts to hypoxia instead of I/R, and which report conflicting results. Here, we present a model of simulated ischaemia/reperfusion (SI/R) to recapitulate the pathophysiological events of early-onset pre-eclampsia (PE), by exposing first trimester cytotrophoblast HTR-8/SVneo cells to a simulated ischaemia buffer followed by reperfusion. We examined different ischaemia and reperfusion times and observed that 1 h ischaemia and 24 h reperfusion induced an increase in reactive oxygen species (ROS) production (P<0.0001) and oxygen consumption rate (P<0.01). SI/R-exposed trophoblast cells exhibited deficits in migration, proliferation, and invasion (P<0.01). While the deficits in migration and proliferation were rescued by antioxidants, suggesting an ROS-dependent mechanism, the loss of invasion was not affected by antioxidants, which suggests a divergent ROS-independent pathway. In line with this, we observed a decrease in MMP-9, the key regulatory enzyme necessary for trophoblast invasion (P<0.01), which was similarly unaffected by antioxidants, and pharmacological inhibition of MMP-9 replicated the phenotype of deficient invasion (P<0.01). Collectively, these data demonstrate that I/R impairs trophoblast migration and proliferation via a ROS-dependent mechanism, and invasion via an ROS-independent loss of MMP-9, disambiguating the role of oxidative stress and providing insights into the response of trophoblasts to I/R in the context of early-onset PE.

Keywords: cell invasion; cell migration; ischemia; metalloproteases; oxidative stress; preeclampsia.

MeSH terms

  • Cell Line
  • Cell Movement*
  • Cell Proliferation
  • Female
  • Humans
  • Matrix Metalloproteinase 9* / metabolism
  • Oxidative Stress*
  • Pre-Eclampsia* / genetics
  • Pre-Eclampsia* / metabolism
  • Pre-Eclampsia* / pathology
  • Pregnancy
  • Pregnancy Trimester, First
  • Reactive Oxygen Species* / metabolism
  • Reperfusion Injury* / genetics
  • Reperfusion Injury* / metabolism
  • Reperfusion Injury* / pathology
  • Trophoblasts* / metabolism
  • Trophoblasts* / pathology

Substances

  • Matrix Metalloproteinase 9
  • Reactive Oxygen Species
  • MMP9 protein, human