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寨卡病毒通过激活 GSDME 引起胎盘细胞焦亡和相关的不良胎儿结局。

Zika virus causes placental pyroptosis and associated adverse fetal outcomes by activating GSDME.

机构信息

State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.

Key Laboratory of Preventive Veterinary Medicine in Hubei Province, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.

出版信息

Elife. 2022 Aug 16;11:e73792. doi: 10.7554/eLife.73792.

Abstract

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.

摘要

寨卡病毒(ZIKV)可在怀孕期间由母体传播给胎儿,导致不良的胎儿结局。有几项研究表明,寨卡病毒可直接损害胎儿大脑;然而,寨卡病毒引起的母体胎盘损伤是否导致不良的胎儿结局尚不清楚。在这里,我们证明寨卡病毒通过体外和体内激活执行者 Gasdermin E(GSDME)导致胎盘细胞发生细胞焦亡。在机制上,病毒基因组 RNA 被 RIG-I 识别后诱导 TNF-α 释放,随后激活 caspase-8 和 caspase-3,最终导致 GSDME 切割。进一步的分析表明,在感染寨卡病毒的怀孕小鼠中敲除 GSDME 或用 TNF-α 受体拮抗剂治疗可减轻胎盘细胞焦亡,从而防止不良的胎儿结局。总之,我们的研究揭示了寨卡病毒通过引起胎盘细胞焦亡导致不良胎儿结局的新机制,为寨卡病毒相关疾病的治疗提供了新线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45ff/9381041/ba51b7f25b12/elife-73792-fig1.jpg

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