• 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

纳米颗粒的生物学特性:蛋白质冠层的形成及其与免疫系统的相互作用。

Biological Features of Nanoparticles: Protein Corona Formation and Interaction with the Immune System.

作者信息

Panico Sonia, Capolla Sara, Bozzer Sara, Toffoli Giuseppe, Dal Bo Michele, Macor Paolo

机构信息

Department of Life Sciences, University of Trieste, 34127 Trieste, Italy.

Experimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico di Aviano (CRO), Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 33081 Aviano, Italy.

出版信息

Pharmaceutics. 2022 Nov 26;14(12):2605. doi: 10.3390/pharmaceutics14122605.

DOI:10.3390/pharmaceutics14122605
PMID:36559099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9781747/
Abstract

Nanoparticles (NPs) are versatile candidates for nanomedical applications due to their unique physicochemical properties. However, their clinical applicability is hindered by their undesirable recognition by the immune system and the consequent immunotoxicity, as well as their rapid clearance in vivo. After injection, NPs are usually covered with layers of proteins, called protein coronas (PCs), which alter their identity, biodistribution, half-life, and efficacy. Therefore, the characterization of the PC is for in predicting the fate of NPs in vivo. The aim of this review was to summarize the state of the art regarding the intrinsic factors closely related to the NP structure, and extrinsic factors that govern PC formation in vitro. In addition, well-known opsonins, including complement, immunoglobulins, fibrinogen, and dysopsonins, such as histidine-rich glycoprotein, apolipoproteins, and albumin, are described in relation to their role in NP detection by immune cells. Particular emphasis is placed on their role in mediating the interaction of NPs with innate and adaptive immune cells. Finally, strategies to reduce PC formation are discussed in detail.

摘要

纳米颗粒(NPs)因其独特的物理化学性质,是纳米医学应用的多功能候选物。然而,它们的临床适用性受到免疫系统对其不良识别以及随之而来的免疫毒性的阻碍,同时还受到其在体内快速清除的影响。注射后,纳米颗粒通常会被称为蛋白质冠(PCs)的蛋白质层覆盖,这会改变它们的特性、生物分布、半衰期和功效。因此,蛋白质冠的表征对于预测纳米颗粒在体内的命运至关重要。本综述的目的是总结与纳米颗粒结构密切相关的内在因素以及体外控制蛋白质冠形成的外在因素的研究现状。此外,还描述了包括补体、免疫球蛋白、纤维蛋白原等著名的调理素,以及富含组氨酸的糖蛋白、载脂蛋白和白蛋白等失调理素在免疫细胞检测纳米颗粒中的作用。特别强调了它们在介导纳米颗粒与先天性和适应性免疫细胞相互作用中的作用。最后,详细讨论了减少蛋白质冠形成的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/42e4a87758ae/pharmaceutics-14-02605-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/2ab3571becfd/pharmaceutics-14-02605-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/b92af0fc3607/pharmaceutics-14-02605-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/27717f5f21ac/pharmaceutics-14-02605-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/83b1519abf61/pharmaceutics-14-02605-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/814850bc1ecf/pharmaceutics-14-02605-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/f5012f10141e/pharmaceutics-14-02605-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/7f7ddf90f4be/pharmaceutics-14-02605-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/332cb1ffe6d9/pharmaceutics-14-02605-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/42e4a87758ae/pharmaceutics-14-02605-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/2ab3571becfd/pharmaceutics-14-02605-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/b92af0fc3607/pharmaceutics-14-02605-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/27717f5f21ac/pharmaceutics-14-02605-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/83b1519abf61/pharmaceutics-14-02605-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/814850bc1ecf/pharmaceutics-14-02605-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/f5012f10141e/pharmaceutics-14-02605-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/7f7ddf90f4be/pharmaceutics-14-02605-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/332cb1ffe6d9/pharmaceutics-14-02605-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a17/9781747/42e4a87758ae/pharmaceutics-14-02605-g009.jpg

相似文献

1
Biological Features of Nanoparticles: Protein Corona Formation and Interaction with the Immune System.纳米颗粒的生物学特性:蛋白质冠层的形成及其与免疫系统的相互作用。
Pharmaceutics. 2022 Nov 26;14(12):2605. doi: 10.3390/pharmaceutics14122605.
2
The protein corona and its effects on nanoparticle-based drug delivery systems.蛋白质冠及其对基于纳米粒子的药物传递系统的影响。
Acta Biomater. 2021 Jul 15;129:57-72. doi: 10.1016/j.actbio.2021.05.019. Epub 2021 May 25.
3
Insights into colloidal nanoparticle-protein corona interactions for nanomedicine applications.用于纳米医学应用的胶体纳米颗粒-蛋白质冠相互作用的深入了解。
Adv Colloid Interface Sci. 2021 Mar;289:102366. doi: 10.1016/j.cis.2021.102366. Epub 2021 Jan 20.
4
The interaction between nanoparticles-protein corona complex and cells and its toxic effect on cells.纳米颗粒-蛋白冠复合物与细胞的相互作用及其对细胞的毒性作用。
Chemosphere. 2020 Apr;245:125624. doi: 10.1016/j.chemosphere.2019.125624. Epub 2019 Dec 12.
5
The importance of selecting a proper biological milieu for protein corona analysis in vitro: Human plasma versus human serum.为体外蛋白质冠层分析选择合适生物环境的重要性:人血浆与人血清的比较。
Int J Biochem Cell Biol. 2016 Jun;75:188-95. doi: 10.1016/j.biocel.2015.11.019. Epub 2015 Nov 28.
6
Insights into Characterization Methods and Biomedical Applications of Nanoparticle-Protein Corona.纳米颗粒-蛋白质冠层的表征方法及生物医学应用洞察
Materials (Basel). 2020 Jul 10;13(14):3093. doi: 10.3390/ma13143093.
7
Opsonins and Dysopsonins of Nanoparticles: Facts, Concepts, and Methodological Guidelines.纳米颗粒的调理蛋白和去调理蛋白:事实、概念和方法学指南。
Front Immunol. 2020 Oct 12;11:567365. doi: 10.3389/fimmu.2020.567365. eCollection 2020.
8
Potential clinical applications of the personalized, disease-specific protein corona on nanoparticles.个性化、疾病特异性蛋白冠在纳米颗粒上的潜在临床应用。
Clin Chim Acta. 2020 Feb;501:102-111. doi: 10.1016/j.cca.2019.10.027. Epub 2019 Oct 31.
9
Nano-Bio Interactions in Cancer: From Therapeutics Delivery to Early Detection.纳米-生物相互作用在癌症中的应用:从治疗药物传递到早期检测。
Acc Chem Res. 2021 Jan 19;54(2):291-301. doi: 10.1021/acs.accounts.0c00413. Epub 2020 Nov 12.
10
Effect of the protein corona on nanoparticles for modulating cytotoxicity and immunotoxicity.蛋白质冠层对纳米颗粒调节细胞毒性和免疫毒性的影响。
Int J Nanomedicine. 2014 Dec 18;10:97-113. doi: 10.2147/IJN.S72998. eCollection 2015.

引用本文的文献

1
The interactions of non-functionalized polystyrene nanoparticles with human albumin and erythrocyte proteins: implications and potential consequences.非功能化聚苯乙烯纳米颗粒与人类白蛋白和红细胞蛋白的相互作用:影响及潜在后果
Sci Rep. 2025 Aug 17;15(1):30076. doi: 10.1038/s41598-025-15422-w.
2
PEGylating AgS Semiconductor Nanocrystals for Pharmacokinetics Tracking: Insights from NIR Luminescence Imaging.用于药代动力学追踪的聚乙二醇化硫化银半导体纳米晶体:近红外发光成像的见解
ACS Omega. 2025 Jun 26;10(26):28351-28361. doi: 10.1021/acsomega.5c03435. eCollection 2025 Jul 8.
3
Evaluating Biocompatibility: From Classical Techniques to State-of-the-Art Functional Proteomics.

本文引用的文献

1
Plasminogen activator-coated nanobubbles targeting cellbound β2-glycoprotein I as a novel thrombus-specific thrombolytic strategy.针对细胞结合β2-糖蛋白 I 的纤溶酶原涂层纳米气泡作为一种新型血栓特异性溶栓策略。
Haematologica. 2023 Jul 1;108(7):1861-1872. doi: 10.3324/haematol.2022.281505.
2
Nanocarriers as a Delivery Platform for Anticancer Treatment: Biological Limits and Perspectives in B-Cell Malignancies.作为抗癌治疗递送平台的纳米载体:B细胞恶性肿瘤的生物学局限与前景
Pharmaceutics. 2022 Sep 17;14(9):1965. doi: 10.3390/pharmaceutics14091965.
3
Zebrafish: A Useful Animal Model for the Characterization of Drug-Loaded Polymeric NPs.
评估生物相容性:从经典技术到最先进的功能蛋白质组学
Nanomaterials (Basel). 2025 Jul 3;15(13):1032. doi: 10.3390/nano15131032.
4
Riding the wave of innovation: nanotechnology in nucleic acid-based cancer therapy.乘创新之浪:基于核酸的癌症治疗中的纳米技术
3 Biotech. 2025 Jul;15(7):226. doi: 10.1007/s13205-025-04397-0. Epub 2025 Jun 27.
5
The Protein Corona Paradox: Challenges in Achieving True Biomimetics in Nanomedicines.蛋白质冠层悖论:纳米药物中实现真正仿生学面临的挑战。
Biomimetics (Basel). 2025 Apr 29;10(5):276. doi: 10.3390/biomimetics10050276.
6
Nanoparticles in Antibacterial Therapy: A Systematic Review of Enhanced Efficacy against Intracellular Bacteria.纳米颗粒在抗菌治疗中的应用:针对细胞内细菌增强疗效的系统评价
ACS Omega. 2025 Apr 25;10(17):17070-17086. doi: 10.1021/acsomega.5c01813. eCollection 2025 May 6.
7
Engineered nanoparticles for imaging and targeted drug delivery in hepatocellular carcinoma.用于肝细胞癌成像和靶向药物递送的工程纳米颗粒。
Exp Hematol Oncol. 2025 Apr 30;14(1):62. doi: 10.1186/s40164-025-00658-z.
8
Development of Iron Oxide Nanochains as a Sensitive Magnetic Particle Imaging Tracer for Cancer Detection.氧化铁纳米链作为用于癌症检测的灵敏磁性粒子成像示踪剂的研发。
ACS Appl Mater Interfaces. 2025 Apr 9;17(14):20859-20871. doi: 10.1021/acsami.5c00332. Epub 2025 Mar 26.
9
DNA-loaded targeted nanoparticles as a safe platform to produce exogenous proteins in tumor B cells.负载DNA的靶向纳米颗粒作为在肿瘤B细胞中产生外源蛋白的安全平台。
Front Immunol. 2025 Jan 22;15:1509322. doi: 10.3389/fimmu.2024.1509322. eCollection 2024.
10
Inflammatory disease progression shapes nanoparticle biomolecular corona-mediated immune activation profiles.炎症性疾病进展塑造了纳米颗粒生物分子冠介导的免疫激活谱。
Nat Commun. 2025 Jan 22;16(1):924. doi: 10.1038/s41467-025-56210-4.
斑马鱼:用于表征载药聚合物纳米颗粒的有用动物模型。
Biomedicines. 2022 Sep 11;10(9):2252. doi: 10.3390/biomedicines10092252.
4
Nanoparticle elasticity affects systemic circulation lifetime by modulating adsorption of apolipoprotein A-I in corona formation.纳米颗粒的弹性通过调节在形成冠时的载脂蛋白 A-I 的吸附来影响全身循环寿命。
Nat Commun. 2022 Jul 16;13(1):4137. doi: 10.1038/s41467-022-31882-4.
5
Temperature, concentration, and surface modification influence the cellular uptake and the protein corona of polystyrene nanoparticles.温度、浓度和表面修饰会影响聚苯乙烯纳米粒子的细胞摄取和蛋白质冠。
Acta Biomater. 2022 Aug;148:271-278. doi: 10.1016/j.actbio.2022.06.028. Epub 2022 Jun 19.
6
Block Length-Dependent Protein Fouling on Poly(2-oxazoline)-Based Polymersomes: Influence on Macrophage Association and Circulation Behavior.聚(2-恶唑啉)基聚合物囊泡上的长度依赖性蛋白质污垢:对巨噬细胞关联和循环行为的影响。
Small. 2022 Jul;18(27):e2201993. doi: 10.1002/smll.202201993. Epub 2022 Jun 7.
7
Nanoparticles Surface Chemistry Influence on Protein Corona Composition and Inflammatory Responses.纳米颗粒表面化学对蛋白质冠层组成和炎症反应的影响。
Nanomaterials (Basel). 2022 Feb 18;12(4):682. doi: 10.3390/nano12040682.
8
The Interactions between Nanoparticles and the Innate Immune System from a Nanotechnologist Perspective.从纳米技术专家视角看纳米颗粒与天然免疫系统之间的相互作用
Nanomaterials (Basel). 2021 Nov 6;11(11):2991. doi: 10.3390/nano11112991.
9
Temperature-Responsive Nanoparticles Enable Specific Binding of Apolipoproteins from Human Plasma.温度响应型纳米颗粒能够特异性结合人血浆中的载脂蛋白。
Small. 2022 Jan;18(3):e2103138. doi: 10.1002/smll.202103138. Epub 2021 Nov 10.
10
Evolution of the protein corona affects macrophage polarization.蛋白质冠的演变会影响巨噬细胞的极化。
Int J Biol Macromol. 2021 Nov 30;191:192-200. doi: 10.1016/j.ijbiomac.2021.09.081. Epub 2021 Sep 20.