• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

寨卡病毒感染胎盘中 TAM 和 TIM 受体 mRNA 的表达。

TAM and TIM receptors mRNA expression in Zika virus infected placentas.

机构信息

Department of Genetics, Evolution, Microbiology and Immunology, Institute of Biology, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil; Department of Obstetrics and Gynecology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.

Department of Genetics, Evolution, Microbiology and Immunology, Institute of Biology, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.

出版信息

Placenta. 2020 Nov;101:204-207. doi: 10.1016/j.placenta.2020.09.062. Epub 2020 Sep 28.

DOI:10.1016/j.placenta.2020.09.062
PMID:33011564
Abstract

To investigate the role of TYRO3, AXL and TIM1 receptors in the Zika virus (ZIKV) cycle, we determined their mRNA expression in different placental sites of ZIKV infected tissue during pregnancy. Unexpectedly, the ZIKV infection was not related with mRNA upregulation of these receptors or changes in expression of type I and III interferons in different placental sites. Instead, a decrease of TYRO3 mRNA expression was observed in positive sites of ZIKV positive placentas in comparison to negative sites. The basis of this downregulation can help to understand how ZIKV persists in placental tissue during pregnancy.

摘要

为了研究 TYRO3、AXL 和 TIM1 受体在 Zika 病毒(ZIKV)周期中的作用,我们在妊娠期间确定了它们在不同胎盘组织中 ZIKV 感染组织中的 mRNA 表达。出乎意料的是,ZIKV 感染与这些受体的 mRNA 上调无关,也与不同胎盘部位的 I 型和 III 型干扰素的表达变化无关。相反,与 ZIKV 阴性胎盘的阳性部位相比,ZIKV 阳性胎盘的 TYRO3 mRNA 表达减少。这种下调的基础有助于了解 ZIKV 如何在妊娠期间在胎盘组织中持续存在。

相似文献

1
TAM and TIM receptors mRNA expression in Zika virus infected placentas.寨卡病毒感染胎盘中 TAM 和 TIM 受体 mRNA 的表达。
Placenta. 2020 Nov;101:204-207. doi: 10.1016/j.placenta.2020.09.062. Epub 2020 Sep 28.
2
TAM Receptors Are Not Required for Zika Virus Infection in Mice.寨卡病毒感染小鼠不需要TAM受体。
Cell Rep. 2017 Apr 18;19(3):558-568. doi: 10.1016/j.celrep.2017.03.058.
3
Axl Promotes Zika Virus Entry and Modulates the Antiviral State of Human Sertoli Cells.Axl 促进寨卡病毒进入并调节人睾丸支持细胞的抗病毒状态。
mBio. 2019 Jul 16;10(4):e01372-19. doi: 10.1128/mBio.01372-19.
4
Characterization of zika virus infection of human fetal cardiac mesenchymal stromal cells.人胚心脏间充质基质细胞感染寨卡病毒的特性。
PLoS One. 2020 Sep 17;15(9):e0239238. doi: 10.1371/journal.pone.0239238. eCollection 2020.
5
Zika Virus Targets Different Primary Human Placental Cells, Suggesting Two Routes for Vertical Transmission.寨卡病毒靶向不同的原代人胎盘细胞,提示垂直传播的两条途径。
Cell Host Microbe. 2016 Aug 10;20(2):155-66. doi: 10.1016/j.chom.2016.07.002. Epub 2016 Jul 18.
6
Type I interferons instigate fetal demise after Zika virus infection.寨卡病毒感染后 I 型干扰素引发胎儿死亡。
Sci Immunol. 2018 Jan 5;3(19). doi: 10.1126/sciimmunol.aao1680.
7
Zika Virus Infects Early- and Midgestation Human Maternal Decidual Tissues, Inducing Distinct Innate Tissue Responses in the Maternal-Fetal Interface.寨卡病毒感染人类妊娠早期和中期的母体蜕膜组织,在母胎界面诱导不同的先天性组织反应。
J Virol. 2017 Jan 31;91(4). doi: 10.1128/JVI.01905-16. Print 2017 Feb 15.
8
Biology of Zika Virus Infection in Human Skin Cells.寨卡病毒在人类皮肤细胞中的感染生物学
J Virol. 2015 Sep;89(17):8880-96. doi: 10.1128/JVI.00354-15. Epub 2015 Jun 17.
9
Type III Interferons Produced by Human Placental Trophoblasts Confer Protection against Zika Virus Infection.人胎盘滋养层细胞产生的III型干扰素可抵御寨卡病毒感染。
Cell Host Microbe. 2016 May 11;19(5):705-12. doi: 10.1016/j.chom.2016.03.008. Epub 2016 Apr 5.
10
Axl is not an indispensable factor for Zika virus infection in mice.Axl并非小鼠感染寨卡病毒的必需因子。
J Gen Virol. 2017 Aug;98(8):2061-2068. doi: 10.1099/jgv.0.000886. Epub 2017 Aug 8.

引用本文的文献

1
Lipid Droplets: Formation, Degradation, and Their Role in Cellular Responses to Flavivirus Infections.脂滴:形成、降解及其在细胞对黄病毒感染反应中的作用
Microorganisms. 2024 Mar 24;12(4):647. doi: 10.3390/microorganisms12040647.
2
Astrocytes derived from neural progenitor cells are susceptible to Zika virus infection.神经祖细胞衍生的星形胶质细胞易感染寨卡病毒。
PLoS One. 2023 Mar 29;18(3):e0283429. doi: 10.1371/journal.pone.0283429. eCollection 2023.
3
Decreased CSTB, RAGE, and Axl Receptor Are Associated with Zika Infection in the Human Placenta.
CSTB、RAGE 和 Axl 受体表达降低与 Zika 病毒感染胎盘有关。
Cells. 2022 Nov 16;11(22):3627. doi: 10.3390/cells11223627.
4
miR-142 Targets TIM-1 in Human Endothelial Cells: Potential Implications for Stroke, COVID-19, Zika, Ebola, Dengue, and Other Viral Infections.miR-142 靶向人内皮细胞中的 TIM-1:对中风、COVID-19、寨卡、埃博拉、登革热和其他病毒感染的潜在影响。
Int J Mol Sci. 2022 Sep 6;23(18):10242. doi: 10.3390/ijms231810242.
5
Monocytes and macrophages in pregnancy: The good, the bad, and the ugly.妊娠期间的单核细胞和巨噬细胞:有好有坏,还有丑陋的。
Immunol Rev. 2022 Jul;308(1):77-92. doi: 10.1111/imr.13080. Epub 2022 Apr 21.
6
Zika Virus Overview: Transmission, Origin, Pathogenesis, Animal Model and Diagnosis.寨卡病毒概述:传播、起源、发病机制、动物模型及诊断
Zoonoses. 2021;1(1). doi: 10.15212/zoonoses-2021-0017. Epub 2021 Dec 7.