• 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

相似文献

1
Cell death mechanisms involved in cell injury caused by SARS-CoV-2.细胞死亡机制涉及 SARS-CoV-2 引起的细胞损伤。
Rev Med Virol. 2022 May;32(3):e2292. doi: 10.1002/rmv.2292. Epub 2021 Sep 30.
2
Putative mechanism of neurological damage in COVID-19 infection.新冠病毒感染导致神经损伤的推测机制。
Acta Neurobiol Exp (Wars). 2021;81(1):69-79. doi: 10.21307/ane-2021-008.
3
Human and novel coronavirus infections in children: a review.儿童人感染和新型冠状病毒感染:综述。
Paediatr Int Child Health. 2021 Feb;41(1):36-55. doi: 10.1080/20469047.2020.1781356. Epub 2020 Jun 25.
4
Potential pathogenesis of severe acute respiratory syndrome coronavirus 2.严重急性呼吸综合征冠状病毒2的潜在发病机制。
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2020 May 28;45(5):591-597. doi: 10.11817/j.issn.1672-7347.2020.200299.
5
COVID-19 and its effects on the digestive system.新型冠状病毒肺炎及其对消化系统的影响。
World J Gastroenterol. 2021 Jun 28;27(24):3502-3515. doi: 10.3748/wjg.v27.i24.3502.
6
2019-Novel Coronavirus-Related Acute Cardiac Injury Cannot Be Ignored.2019 新型冠状病毒相关急性心脏损伤不容忽视。
Curr Atheroscler Rep. 2020 May 7;22(3):14. doi: 10.1007/s11883-020-00842-y.
7
Coronavirus disease 2019 and asthma, allergic rhinitis: molecular mechanisms and host-environmental interactions.新型冠状病毒病 2019 与哮喘、变应性鼻炎:分子机制与宿主-环境相互作用。
Curr Opin Allergy Clin Immunol. 2021 Feb 1;21(1):1-7. doi: 10.1097/ACI.0000000000000699.
8
Coronavirus Disease 2019: Coronaviruses and Kidney Injury.2019 年冠状病毒病:冠状病毒与肾脏损伤。
J Urol. 2020 Nov;204(5):918-925. doi: 10.1097/JU.0000000000001289. Epub 2020 Jul 17.
9
SARS-CoV-2 Causes Lung Infection without Severe Disease in Human ACE2 Knock-In Mice.SARS-CoV-2 引起人类 ACE2 基因敲入小鼠肺部感染但不引起严重疾病。
J Virol. 2022 Jan 12;96(1):e0151121. doi: 10.1128/JVI.01511-21. Epub 2021 Oct 20.
10
Does SARS-Cov-2 invade the brain? Translational lessons from animal models.SARS-CoV-2 是否侵犯大脑?动物模型的转化研究。
Eur J Neurol. 2020 Sep;27(9):1764-1773. doi: 10.1111/ene.14277. Epub 2020 May 22.

引用本文的文献

1
Cytogenetic Alterations Observed in Exfoliative Cells of the Tongue and Oral Mucosa of SARS-CoV-2-Vaccinated Patients: Report of Two Cases and a Brief Literature Review.在接种新冠病毒疫苗患者的舌部和口腔黏膜脱落细胞中观察到的细胞遗传学改变:两例报告及文献简要综述
Rev Soc Bras Med Trop. 2025 Jun 2;58:e008042025. doi: 10.1590/0037-8682-0008-2025. eCollection 2025.
2
New Onset of Type 1 and Type 2 Diabetes Post-COVID-19 Infection: A Systematic Review.新冠病毒感染后1型和2型糖尿病的新发:一项系统综述
Emerg Microbes Infect. 2025 May 6:2492211. doi: 10.1080/22221751.2025.2492211.
3
IL-1β drives SARS-CoV-2-induced disease independently of the inflammasome and pyroptosis signalling.白细胞介素-1β独立于炎性小体和细胞焦亡信号传导驱动新冠病毒诱导的疾病。
Cell Death Differ. 2025 Feb 28. doi: 10.1038/s41418-025-01459-x.
4
The Role of Inflammation in the Pathogenesis of Viral Respiratory Infections.炎症在病毒性呼吸道感染发病机制中的作用
Microorganisms. 2024 Dec 7;12(12):2526. doi: 10.3390/microorganisms12122526.
5
The role of reactive oxygen species in severe acute respiratory syndrome coronavirus 2 (SARS-COV-2) infection-induced cell death.活性氧在严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染诱导的细胞死亡中的作用。
Cell Mol Biol Lett. 2024 Nov 8;29(1):138. doi: 10.1186/s11658-024-00659-6.
6
Cerebral small vessel injury in mice with damage to ACE2-expressing cerebral vascular endothelial cells and post COVID-19 patients.脑内小血管损伤与 ACE2 表达的脑血管内皮细胞损伤和新冠病毒感染后患者相关。
Alzheimers Dement. 2024 Nov;20(11):7971-7988. doi: 10.1002/alz.14279. Epub 2024 Oct 1.
7
The Role of the Nrf2 Pathway in Airway Tissue Damage Due to Viral Respiratory Infections.Nrf2 通路在病毒呼吸道感染导致的气道组织损伤中的作用。
Int J Mol Sci. 2024 Jun 27;25(13):7042. doi: 10.3390/ijms25137042.
8
Pathophysiological, immunological, and inflammatory features of long COVID.长新冠的病理生理、免疫和炎症特征。
Front Immunol. 2024 Feb 28;15:1341600. doi: 10.3389/fimmu.2024.1341600. eCollection 2024.
9
Necroptosis does not drive disease pathogenesis in a mouse infective model of SARS-CoV-2 in vivo.细胞程序性坏死不会在 SARS-CoV-2 的感染性小鼠模型中驱动疾病发病机制。
Cell Death Dis. 2024 Jan 30;15(1):100. doi: 10.1038/s41419-024-06471-6.
10
Assessment of Genotoxic Biomarker in Tongue and Buccal Mucosal Epithelial Cells of COVID-19 Patients: An Observational Study.新冠病毒肺炎患者舌及颊黏膜上皮细胞遗传毒性生物标志物的评估:一项观察性研究
Cureus. 2023 Nov 12;15(11):e48706. doi: 10.7759/cureus.48706. eCollection 2023 Nov.

本文引用的文献

1
SARS-CoV-2 engages inflammasome and pyroptosis in human primary monocytes.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)在人原代单核细胞中激活炎性小体并引发细胞焦亡。
Cell Death Discov. 2021 Mar 1;7(1):43. doi: 10.1038/s41420-021-00428-w.
2
Supporting SARS-CoV-2 Papain-Like Protease Drug Discovery: Methods and Benchmarking.支持严重急性呼吸综合征冠状病毒2型木瓜样蛋白酶药物研发:方法与基准测试
Front Chem. 2020 Nov 5;8:592289. doi: 10.3389/fchem.2020.592289. eCollection 2020.
3
Inflammasomes are activated in response to SARS-CoV-2 infection and are associated with COVID-19 severity in patients.炎症小体在 SARS-CoV-2 感染时被激活,并与 COVID-19 患者的严重程度相关。
J Exp Med. 2021 Mar 1;218(3). doi: 10.1084/jem.20201707.
4
Severe COVID-19: what have we learned with the immunopathogenesis?严重的 COVID-19:我们从免疫发病机制中学到了什么?
Adv Rheumatol. 2020 Sep 22;60(1):50. doi: 10.1186/s42358-020-00151-7.
5
Understanding genomic diversity, pan-genome, and evolution of SARS-CoV-2.了解严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的基因组多样性、泛基因组和进化。
PeerJ. 2020 Jul 17;8:e9576. doi: 10.7717/peerj.9576. eCollection 2020.
6
Increased CD95 (Fas) and PD-1 expression in peripheral blood T lymphocytes in COVID-19 patients.COVID-19 患者外周血 T 淋巴细胞中 CD95(Fas)和 PD-1 的表达增加。
Br J Haematol. 2020 Oct;191(2):207-211. doi: 10.1111/bjh.17034. Epub 2020 Aug 18.
7
Canonical and Noncanonical Autophagy as Potential Targets for COVID-19.规范和非规范自噬作为 COVID-19 的潜在靶点。
Cells. 2020 Jul 5;9(7):1619. doi: 10.3390/cells9071619.
8
Autophagy and SARS-CoV-2 infection: Apossible smart targeting of the autophagy pathway.自噬与 SARS-CoV-2 感染:自噬途径的一种潜在靶向策略。
Virulence. 2020 Dec;11(1):805-810. doi: 10.1080/21505594.2020.1780088.
9
The ORF3a protein of SARS-CoV-2 induces apoptosis in cells.新型冠状病毒(SARS-CoV-2)的ORF3a蛋白可诱导细胞凋亡。
Cell Mol Immunol. 2020 Aug;17(8):881-883. doi: 10.1038/s41423-020-0485-9. Epub 2020 Jun 18.
10
Autophagy as an emerging target for COVID-19: lessons from an old friend, chloroquine.自噬作为 COVID-19 的新兴靶点:来自老朋友氯喹的启示。
Autophagy. 2020 Dec;16(12):2260-2266. doi: 10.1080/15548627.2020.1779467. Epub 2020 Jun 24.

细胞死亡机制涉及 SARS-CoV-2 引起的细胞损伤。

Cell death mechanisms involved in cell injury caused by SARS-CoV-2.

机构信息

Research Center for Therapeutic Innovation Suely Galdino, Federal University of Pernambuco, Recife, Brazil.

Universidade Federal Rural de Pernambuco, Recife, Brazil.

出版信息

Rev Med Virol. 2022 May;32(3):e2292. doi: 10.1002/rmv.2292. Epub 2021 Sep 30.

DOI:10.1002/rmv.2292
PMID:34590761
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8646768/
Abstract

Coronavirus disease 2019 (Covid-19) is an emerging novel respiratory infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that rapidly spread worldwide. In addition to lung injury, Covid-19 patients may develop extrapulmonary symptoms, including cardiac, liver, kidney, digestive tract, and neurological injuries. Angiotensin converting enzyme 2 is the major receptor for the entry of SARS-CoV-2 into host cells. The specific mechanisms that lead to cell death in different tissues during infection by SARS-CoV-2 remains unknown. Based on data of the previous human coronavirus SARS-CoV together with information about SARS-CoV-2, this review provides a summary of the mechanisms involved in cell death, including apoptosis, autophagy, and necrosis, provoked by severe acute respiratory syndrome coronavirus.

摘要

新型冠状病毒病(COVID-19)是一种由严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)引起的新发呼吸道传染病,在全球迅速蔓延。除肺部损伤外,COVID-19 患者还可能出现肺外症状,包括心脏、肝脏、肾脏、消化道和神经系统损伤。血管紧张素转换酶 2 是 SARS-CoV-2 进入宿主细胞的主要受体。SARS-CoV-2 感染导致不同组织细胞死亡的具体机制尚不清楚。基于之前人类冠状病毒 SARS-CoV 的数据以及关于 SARS-CoV-2 的信息,本综述总结了严重急性呼吸综合征冠状病毒引起的细胞死亡机制,包括凋亡、自噬和坏死。