• 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

用于研究 SARS-CoV-2 感染性和抗病毒候选物的 3D 培养模型:从球体到生物打印。

3D culture models to study SARS-CoV-2 infectivity and antiviral candidates: From spheroids to bioprinting.

机构信息

Department of Biochemistry, Paulista School of Medicine, Universidade Federal de São Paulo, São Paulo, Brazil.

Department of Microbiology, Immunology and Parasitology, Paulista School of Medicine, Universidade Federal de São Paulo, São Paulo, Brazil.

出版信息

Biomed J. 2021 Mar;44(1):31-42. doi: 10.1016/j.bj.2020.11.009. Epub 2020 Nov 21.

DOI:10.1016/j.bj.2020.11.009
PMID:33602633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7680063/
Abstract

The pandemic caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is receiving worldwide attention, due to the severity of the disease (COVID-19) that resulted in more than a million global deaths so far. The urgent need for vaccines and antiviral drugs is mobilizing the scientific community to develop strategies for studying the mechanisms of SARS-CoV-2 infection, replication kinetics, pathogenesis, host-virus interaction, and infection inhibition. In this work, we review the strategies of tissue engineering in the fabrication of three-dimensional (3D) models used in virology studies, which presented many advantages over conventional cell cultures, such as complex cytoarchitecture and a more physiological microenvironment. Scaffold-free (spheroids and organoids) and scaffold-based (3D scaffolding and 3D bioprinting) approach allow the biofabrication of more realistic models relevant to the pandemic, to be used as in vitro platforms for the development of new vaccines and therapies against COVID-19.

摘要

由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的大流行引起了全世界的关注,因为由此导致的疾病(COVID-19)迄今已在全球造成超过 100 万人死亡。对疫苗和抗病毒药物的迫切需求促使科学界制定研究 SARS-CoV-2 感染、复制动力学、发病机制、宿主-病毒相互作用和感染抑制机制的策略。在这项工作中,我们回顾了组织工程在病毒学研究中制造三维(3D)模型的策略,这些策略与传统细胞培养相比具有许多优势,例如复杂的细胞结构和更生理的微环境。无支架(球体和类器官)和支架(3D 支架和 3D 生物打印)方法允许生物制造更符合大流行实际情况的模型,用作开发针对 COVID-19 的新疫苗和疗法的体外平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/ff26cd0ec498/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/1ecc24ca1fde/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/71b78a071a2e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/8b8eaec736ea/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/368974eaa20d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/ff26cd0ec498/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/1ecc24ca1fde/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/71b78a071a2e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/8b8eaec736ea/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/368974eaa20d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e465/8103332/ff26cd0ec498/gr5.jpg

相似文献

1
3D culture models to study SARS-CoV-2 infectivity and antiviral candidates: From spheroids to bioprinting.用于研究 SARS-CoV-2 感染性和抗病毒候选物的 3D 培养模型:从球体到生物打印。
Biomed J. 2021 Mar;44(1):31-42. doi: 10.1016/j.bj.2020.11.009. Epub 2020 Nov 21.
2
Spheroids and organoids as humanized 3D scaffold-free engineered tissues for SARS-CoV-2 viral infection and drug screening.球状体和类器官作为无支架 3D 人源化工程组织用于 SARS-CoV-2 病毒感染和药物筛选。
Artif Organs. 2021 Jun;45(6):548-558. doi: 10.1111/aor.13880. Epub 2021 Jan 10.
3
Bioprinting Using Organ Building Blocks: Spheroids, Organoids, and Assembloids.使用器官构建模块进行生物打印:球体、类器官和组装体。
Tissue Eng Part A. 2024 Jul;30(13-14):377-386. doi: 10.1089/ten.TEA.2023.0198. Epub 2024 Jan 25.
4
Bioengineered Tissue Models to Study SARS-CoV-2 Pathogenesis and Therapeutic Validation.生物工程化组织模型用于研究 SARS-CoV-2 发病机制和治疗验证。
ACS Biomater Sci Eng. 2020 Dec 14;6(12):6540-6555. doi: 10.1021/acsbiomaterials.0c01226. Epub 2020 Nov 16.
5
Review of studies of severe acute respiratory syndrome related coronavirus-2 pathogenesis in human organoid models.人类类器官模型中严重急性呼吸综合征相关冠状病毒2发病机制的研究综述。
Rev Med Virol. 2021 Nov;31(6):e2227. doi: 10.1002/rmv.2227. Epub 2021 Mar 25.
6
Strategies for 3D bioprinting of spheroids: A comprehensive review.球形聚集体的 3D 生物打印策略:全面综述。
Biomaterials. 2022 Dec;291:121881. doi: 10.1016/j.biomaterials.2022.121881. Epub 2022 Oct 28.
7
Three-Dimensional Cell Culture Models to Study Respiratory Virus Infections Including COVID-19.用于研究包括 COVID-19 在内的呼吸道病毒感染的三维细胞培养模型
Biomimetics (Basel). 2021 Dec 25;7(1):3. doi: 10.3390/biomimetics7010003.
8
An Adverse Outcomes Approach to Study the Effects of SARS-CoV-2 in 3D Organoid Models.一种利用不良结局方法研究 SARS-CoV-2 在 3D 类器官模型中作用的研究方法。
J Mol Biol. 2022 Feb 15;434(3):167213. doi: 10.1016/j.jmb.2021.167213. Epub 2021 Aug 23.
9
Potential Anti-Coronavirus Agents and the Pharmacologic Mechanisms.潜在的抗冠状病毒药物及其药理学机制。
Drug Des Devel Ther. 2021 Mar 17;15:1213-1223. doi: 10.2147/DDDT.S293216. eCollection 2021.
10
Bioprinting Strategies for Secretory Epithelial Organoids.生物打印策略用于分泌上皮类器官。
Methods Mol Biol. 2020;2140:243-249. doi: 10.1007/978-1-0716-0520-2_16.

引用本文的文献

1
Bioprinted Four-Cell-Type Lung Model for Viral Infection Studies Under Air-Liquid Interface Conditions.用于气液界面条件下病毒感染研究的生物打印四细胞类型肺模型
Int J Mol Sci. 2025 Jun 10;26(12):5543. doi: 10.3390/ijms26125543.
2
First contact: an interdisciplinary guide into decoding H5N1 influenza virus interactions with glycosaminoglycans in 3D respiratory cell models.首次接触:3D呼吸道细胞模型中H5N1流感病毒与糖胺聚糖相互作用解码的跨学科指南。
Front Cell Infect Microbiol. 2025 May 15;15:1596955. doi: 10.3389/fcimb.2025.1596955. eCollection 2025.
3
Sacred codes: Preservation, permutation and expression.

本文引用的文献

1
3D Printed Cartilage-Like Tissue Constructs with Spatially Controlled Mechanical Properties.具有空间可控力学性能的3D打印类软骨组织构建物。
Adv Funct Mater. 2019 Dec 19;29(51). doi: 10.1002/adfm.201906330. Epub 2019 Oct 21.
2
Neuroinvasion of SARS-CoV-2 in human and mouse brain.新冠病毒在人和鼠脑内的神经入侵。
J Exp Med. 2021 Mar 1;218(3). doi: 10.1084/jem.20202135.
3
CD147-spike protein is a novel route for SARS-CoV-2 infection to host cells.CD147-刺突蛋白是 SARS-CoV-2 感染宿主细胞的新途径。
神圣密码:保存、置换与表达。
Biomed J. 2025 Apr 4;48(2):100852. doi: 10.1016/j.bj.2025.100852.
4
Peptides from against spp: toxicity in three-dimensional cell cultures and .来自抗**属**的肽:三维细胞培养中的毒性及**(原文此处不完整)**
Future Microbiol. 2025 Jan;20(1):11-21. doi: 10.1080/17460913.2024.2421632. Epub 2024 Nov 18.
5
Understanding the cellular dynamics, engineering perspectives and translation prospects in bioprinting epithelial tissues.了解生物打印上皮组织中的细胞动力学、工程学观点及转化前景。
Bioact Mater. 2024 Sep 24;43:195-224. doi: 10.1016/j.bioactmat.2024.09.025. eCollection 2025 Jan.
6
High Concentrations of Cannabidiol Induce Neurotoxicity in Neurosphere Culture System.高浓度的大麻二酚在神经球培养系统中诱导神经毒性。
Neurotox Res. 2024 Feb 13;42(1):14. doi: 10.1007/s12640-024-00692-5.
7
Identification of druggable host dependency factors shared by multiple SARS-CoV-2 variants of concern.鉴定多个引起关注的 SARS-CoV-2 变异株共有的可用药宿主依赖性因子。
J Mol Cell Biol. 2024 Aug 26;16(3). doi: 10.1093/jmcb/mjae004.
8
Rising role of 3D-printing in delivery of therapeutics for infectious disease.3D 打印在传染病治疗药物传递中的作用不断提升。
J Control Release. 2024 Feb;366:349-365. doi: 10.1016/j.jconrel.2023.12.051. Epub 2024 Jan 8.
9
Preclinical evaluation of implantable materials: conventional approaches, new models and future directions.可植入材料的临床前评估:传统方法、新模型及未来方向。
Front Bioeng Biotechnol. 2023 Jul 27;11:1193204. doi: 10.3389/fbioe.2023.1193204. eCollection 2023.
10
An integrated - approach for bioprinting core-shell bioarchitectures.一种用于生物打印核壳生物结构的综合方法。
Int J Bioprint. 2023 Jun 12;9(5):771. doi: 10.18063/ijb.771. eCollection 2023.
Signal Transduct Target Ther. 2020 Dec 4;5(1):283. doi: 10.1038/s41392-020-00426-x.
4
Human Pluripotent Stem Cell-Derived Neural Cells and Brain Organoids Reveal SARS-CoV-2 Neurotropism Predominates in Choroid Plexus Epithelium.人多能干细胞衍生的神经细胞和脑类器官揭示 SARS-CoV-2 的嗜神经性主要存在于脉络丛上皮。
Cell Stem Cell. 2020 Dec 3;27(6):937-950.e9. doi: 10.1016/j.stem.2020.09.016. Epub 2020 Sep 21.
5
SARS-CoV-2 targets neurons of 3D human brain organoids.SARS-CoV-2 靶向 3D 人脑组织类器官中的神经元。
EMBO J. 2020 Oct 15;39(20):e106230. doi: 10.15252/embj.2020106230. Epub 2020 Sep 23.
6
Morphogenesis and cytopathic effect of SARS-CoV-2 infection in human airway epithelial cells.SARS-CoV-2 感染人呼吸道上皮细胞的形态发生和细胞病变效应。
Nat Commun. 2020 Aug 6;11(1):3910. doi: 10.1038/s41467-020-17796-z.
7
Infectability of human BrainSphere neurons suggests neurotropism of SARS-CoV-2.人类脑球体神经元的感染性表明了 SARS-CoV-2 的嗜神经性。
ALTEX. 2020;37(4):665-671. doi: 10.14573/altex.2006111. Epub 2020 Jun 26.
8
In Vitro and Animal Models for SARS-CoV-2 research.用于 SARS-CoV-2 研究的体外和动物模型。
Trends Pharmacol Sci. 2020 Aug;41(8):513-517. doi: 10.1016/j.tips.2020.05.005. Epub 2020 May 30.
9
COVID-19: organoids go viral.COVID-19:类器官引发热议。
Nat Rev Mol Cell Biol. 2020 Jul;21(7):355-356. doi: 10.1038/s41580-020-0258-4.
10
Neuropathogenesis and Neurologic Manifestations of the Coronaviruses in the Age of Coronavirus Disease 2019: A Review.新型冠状病毒病 2019 时代冠状病毒的神经发病机制和神经表现:综述。
JAMA Neurol. 2020 Aug 1;77(8):1018-1027. doi: 10.1001/jamaneurol.2020.2065.