• 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

微小核糖核酸病毒诱导的细胞焦亡及其在病毒感染治疗中的潜在作用。

Cell pyroptosis in picornavirus and its potential for treating viral infection.

机构信息

Department of Medical Microbiology, School of Medicine, Nanchang University, Nanchang, China.

Department of Medical Microbiology, School of Queen Mary of Nanchang University, Nanchang, China.

出版信息

J Med Virol. 2022 Aug;94(8):3570-3580. doi: 10.1002/jmv.27813. Epub 2022 May 6.

DOI:10.1002/jmv.27813
PMID:35474513
Abstract

Cell pyroptosis has received increased attention due to the associations between innate immunity and disease, and it has become a major focal point recently due to in-depth studies of cancer. With increased research on pyroptosis, scientists have discovered that it has an essential role in viral infections, especially in the occurrence and development of some picornavirus infections. Many picornaviruses, including Coxsackievirus, a71 enterovirus, human rhinovirus, encephalomyocarditis virus, and foot-and-mouth disease virus induce pyroptosis to varying degrees. This review summarized the mechanisms by which these viruses induce cell pyroptosis, which can be an effective defense against pathogen infection. However, excessive inflammasome activation or pyroptosis also can damage the host's health or aggravate disease progression. Careful approaches that acknowledge this dual effect will aid in the exploration of picornavirus infections and the mechanisms that produce the inflammatory response. This information will promote the development of drugs that can inhibit cell pyroptosis and provide new avenues for future clinical treatment.

摘要

细胞焦亡由于与先天免疫和疾病之间的关联而受到越来越多的关注,并且由于对癌症的深入研究,它最近成为一个主要焦点。随着对细胞焦亡的研究不断增加,科学家们发现它在病毒感染中起着至关重要的作用,尤其是在某些小核糖核酸病毒感染的发生和发展中。许多小核糖核酸病毒,包括柯萨奇病毒 A71 肠病毒、人鼻病毒、脑炎心肌炎病毒和口蹄疫病毒,在不同程度上诱导细胞焦亡。本综述总结了这些病毒诱导细胞焦亡的机制,细胞焦亡可以作为宿主抵抗病原体感染的有效防御机制。然而,过度的炎性体激活或细胞焦亡也会损害宿主的健康或加重疾病进展。认真考虑这种双重作用的方法将有助于探索小核糖核酸病毒感染和产生炎症反应的机制。这些信息将促进抑制细胞焦亡的药物的开发,并为未来的临床治疗提供新途径。

相似文献

1
Cell pyroptosis in picornavirus and its potential for treating viral infection.微小核糖核酸病毒诱导的细胞焦亡及其在病毒感染治疗中的潜在作用。
J Med Virol. 2022 Aug;94(8):3570-3580. doi: 10.1002/jmv.27813. Epub 2022 May 6.
2
NOD-like receptor family, pyrin domain containing 3 (NLRP3) contributes to inflammation, pyroptosis, and mucin production in human airway epithelium on rhinovirus infection.核苷酸结合寡聚化结构域样受体家族,含pyrin 结构域蛋白 3(NLRP3)在鼻病毒感染后促进人呼吸道上皮细胞的炎症、细胞焦亡和粘蛋白产生。
J Allergy Clin Immunol. 2019 Sep;144(3):777-787.e9. doi: 10.1016/j.jaci.2019.05.006. Epub 2019 May 15.
3
NLRP3-dependent pyroptosis exacerbates coxsackievirus A16 and coxsackievirus A10-induced inflammatory response and viral replication in SH-SY5Y cells.NLRP3 依赖性细胞焦亡加剧柯萨奇病毒 A16 和柯萨奇病毒 A10 诱导的 SH-SY5Y 细胞炎症反应和病毒复制。
Virus Res. 2024 Jul;345:199386. doi: 10.1016/j.virusres.2024.199386. Epub 2024 May 6.
4
Pyroptosis induced by enterovirus 71 and coxsackievirus B3 infection affects viral replication and host response.肠病毒 71 型和柯萨奇病毒 B3 感染诱导的细胞焦亡影响病毒复制和宿主反应。
Sci Rep. 2018 Feb 13;8(1):2887. doi: 10.1038/s41598-018-20958-1.
5
Inflammasomes and its importance in viral infections.炎性小体及其在病毒感染中的重要性。
Immunol Res. 2016 Dec;64(5-6):1101-1117. doi: 10.1007/s12026-016-8873-z.
6
Picornaviruses and RNA Metabolism: Local and Global Effects of Infection.小核糖核酸病毒与 RNA 代谢:感染的局部和整体效应。
J Virol. 2019 Oct 15;93(21). doi: 10.1128/JVI.02088-17. Print 2019 Nov 1.
7
NLRP3 Inflammasome-A Key Player in Antiviral Responses.NLRP3 炎性小体:抗病毒反应的关键参与者。
Front Immunol. 2020 Feb 18;11:211. doi: 10.3389/fimmu.2020.00211. eCollection 2020.
8
AIM2 Inflammasome-Mediated Pyroptosis in Enterovirus A71-Infected Neuronal Cells Restricts Viral Replication.目的 2 炎性小体介导的肠道病毒 A71 感染神经元细胞的细胞焦亡限制病毒复制。
Sci Rep. 2017 Jul 19;7(1):5845. doi: 10.1038/s41598-017-05589-2.
9
Activation of the NLRP3 inflammasome and elevation of interleukin-1β secretion in infection by sever fever with thrombocytopenia syndrome virus.严重发热伴血小板减少综合征病毒感染激活 NLRP3 炎症小体并升高白细胞介素-1β 的分泌。
Sci Rep. 2022 Feb 16;12(1):2573. doi: 10.1038/s41598-022-06229-0.
10
Encephalomyocarditis virus viroporin 2B activates NLRP3 inflammasome.脑心肌炎病毒 viroporin 2B 激活 NLRP3 炎症小体。
PLoS Pathog. 2012;8(8):e1002857. doi: 10.1371/journal.ppat.1002857. Epub 2012 Aug 9.

引用本文的文献

1
Ipriflavone ameliorates intervertebral disc degeneration by inhibiting osteoporosis of vertebral body and pyroptosis of the nucleus pulposus in instability of lumbar spine and diabetic mice.依普黄酮通过抑制腰椎不稳和糖尿病小鼠椎体骨质疏松及髓核细胞焦亡来改善椎间盘退变。
Front Bioeng Biotechnol. 2025 Aug 5;13:1639117. doi: 10.3389/fbioe.2025.1639117. eCollection 2025.
2
miR-29b-3p regulates cardiomyocytes pyroptosis in CVB3-induced myocarditis through targeting DNMT3A.miR-29b-3p 通过靶向 DNMT3A 调节柯萨奇病毒 B3 诱导的心肌炎中心肌细胞焦亡。
Cell Mol Biol Lett. 2024 Apr 20;29(1):55. doi: 10.1186/s11658-024-00576-8.
3
The neuropathological mechanism of EV-A71 infection attributes to inflammatory pryoptosis and viral replication via activating the hsa_circ_0045431/ hsa_miR_584/NLRP3 regulatory axis.
肠道病毒 A71 感染的神经病理学机制归因于通过激活 hsa_circ_0045431/hsa_miR_584/NLRP3 调节轴引发的炎症性细胞焦亡和病毒复制。
Virus Res. 2023 Oct 2;335:199195. doi: 10.1016/j.virusres.2023.199195. Epub 2023 Aug 15.
4
Ferroptosis, Necroptosis, and Pyroptosis in Gastrointestinal Cancers: The Chief Culprits of Tumor Progression and Drug Resistance.铁死亡、坏死性凋亡和焦亡在胃肠癌中的作用:肿瘤进展和耐药的主要元凶。
Adv Sci (Weinh). 2023 Sep;10(26):e2300824. doi: 10.1002/advs.202300824. Epub 2023 Jul 12.
5
Foot-and-Mouth Disease Virus Induces Porcine Gasdermin E-Mediated Pyroptosis through the Protease Activity of 3C.口蹄疫病毒通过 3C 蛋白酶活性诱导猪源性 Gasdermin E 介导的细胞焦亡。
J Virol. 2023 Jul 27;97(7):e0068623. doi: 10.1128/jvi.00686-23. Epub 2023 Jun 27.
6
Role of Pyroptosis in Intervertebral Disc Degeneration and Its Therapeutic Implications.焦亡在椎间盘退变中的作用及其治疗意义。
Biomolecules. 2022 Dec 2;12(12):1804. doi: 10.3390/biom12121804.