Procoagulant Extracellular Vesicles Alter Trophoblast Differentiation in Mice by a Thrombo-Inflammatory Mechanism

Int J Mol Sci. 2021 Sep 13;22(18):9873. doi: 10.3390/ijms22189873.

Abstract

Procoagulant extracellular vesicles (EV) and platelet activation have been associated with gestational vascular complications. EV-induced platelet-mediated placental inflammasome activation has been shown to cause preeclampsia-like symptoms in mice. However, the effect of EV-mediated placental thrombo-inflammation on trophoblast differentiation remains unknown. Here, we identify that the EV-induced thrombo-inflammatory pathway modulates trophoblast morphology and differentiation. EVs and platelets reduce syncytiotrophoblast differentiation while increasing giant trophoblast and spongiotrophoblast including the glycogen-rich cells. These effects are platelet-dependent and mediated by the NLRP3 inflammasome. In humans, inflammasome activation was negatively correlated with trophoblast differentiation marker GCM1 and positively correlated with blood pressure. These data identify a crucial role of EV-induced placental thrombo-inflammation on altering trophoblast differentiation and suggest platelet activation or inflammasome activation as a therapeutic target in order to achieve successful placentation.

Keywords: extracellular vesicles; inflammasome; thrombo-inflammation; trophoblast differentiation.

MeSH terms

  • Animals
  • Blood Platelets / metabolism
  • Blood Platelets / pathology
  • Cell Differentiation / genetics
  • DNA-Binding Proteins / genetics
  • Disease Models, Animal
  • Extracellular Vesicles / genetics*
  • Extracellular Vesicles / metabolism
  • Female
  • Humans
  • Inflammasomes / genetics
  • Inflammation / genetics*
  • Inflammation / metabolism
  • Inflammation / pathology
  • Mice
  • NLR Family, Pyrin Domain-Containing 3 Protein / genetics*
  • Platelet Activation / genetics
  • Pregnancy
  • Pregnancy Complications, Cardiovascular / genetics*
  • Pregnancy Complications, Cardiovascular / pathology
  • Transcription Factors / genetics
  • Trophoblasts / metabolism
  • Trophoblasts / pathology

Substances

  • DNA-Binding Proteins
  • Gcm1 protein, mouse
  • Inflammasomes
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Transcription Factors