eLife · 2022 · 67 citations · 61 references
Life SciencesImmunologyNeuroscienceInflammationInnate ImmunityMaternal-fetal MedicineFetal OutcomesNeuroinflammationNeuroprotectionPlacental BiologyPlacental ImmunologyPlacental PhysiologyCell Death Pathways In Viral InfectionMaternal Zika Virus InfectionPlacental CellsPlacental Cytokine SignalingPlacental Signaling PathwaysPyroptosis MechanismsViral Immunity At The Maternal-fetal InterfaceZika Virus Transmission
Zika virus (ZIKV) can be transmitted from mother to fetus during pregnancy, causing adverse fetal outcomes. Several studies have indicated that ZIKV can damage the fetal brain directly; however, whether the ZIKV-induced maternal placental injury contributes to adverse fetal outcomes is sparsely defined. Here, we demonstrated that ZIKV causes the pyroptosis of placental cells by activating the executor gasdermin E (GSDME) in vitro and in vivo. Mechanistically, TNF-α release is induced upon the recognition of viral genomic RNA by RIG-I, followed by activation of caspase-8 and caspase-3 to ultimately escalate the GSDME cleavage. Further analyses revealed that the ablation of GSDME or treatment with TNF-α receptor antagonist in ZIKV-infected pregnant mice attenuates placental pyroptosis, which consequently confers protection against adverse fetal outcomes. In conclusion, our study unveils a novel mechanism of ZIKV-induced adverse fetal outcomes via causing placental cell pyroptosis, which provides new clues for developing therapies for ZIKV-associated diseases.
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