Modulation of macrophage polarization by iron-based nanoparticles-Reference-Cited by-同舟云学术

Modulation of macrophage polarization by iron-based nanoparticles

Published:2023-04-01 Issue:2 Volume:3 Page:105-122
ISSN:2749-9642
Container-title:Medical Review
language:en
Short-container-title:

Author:

Ding He¹,Zhang Yuxin¹,Mao Yu²,Li Yan¹,Shen Yan³,Sheng Jingyi¹^ORCID,Gu Ning¹⁴^ORCID

Affiliation:

1. Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering, Southeast University , Nanjing , Jiangsu Province , China

2. Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School , Nanjing , , China

3. School of Biomedical Engineering and Informatics, Nanjing Medical University , Nanjing , , China

4. Medical School , Nanjing University , Nanjing 210093 , China

Abstract

Abstract Macrophage polarization is an essential process involved in immune regulation. In response to different microenvironmental stimulation, macrophages polarize into cells with different phenotypes and functions, most typically M1 (pro-inflammatory) and M2 (anti-inflammatory) macrophages. Iron-based nanoparticles have been widely explored and reported to regulate macrophage polarization for various biomedical applications. However, the influence factors and modulation mechanisms behind are complicated and not clear. In this review, we systemically summarized different iron-based nanoparticles that regulate macrophage polarization and function and discussed the influence factors and mechanisms underlying the modulation process. This review aims to deepen the understanding of the modulation of macrophage polarization by iron-based nanoparticles and expects to provide evidence and guidance for subsequent design and application of iron-based nanoparticles with specific macrophage modulation functions.

Publisher

Walter de Gruyter GmbH

Link

https://www.degruyter.com/document/doi/10.1515/mr-2023-0002/pdf

Reference114 articles.

1. Laskin, DL, Sunil, VR, Gardner, CR, Laskin, JD. Macrophages and tissue injury: agents of defense or destruction? Annu Rev Pharmacol Toxicol 2011;51:267. https://doi.org/10.1146/annurev.pharmtox.010909.105812.

2. Mondal, P, Anweshan, A, Purkait, MK. Green synthesis and environmental application of iron-based nanomaterials and nanocomposite: a review. Chemosphere 2020;259:127509. https://doi.org/10.1016/j.chemosphere.2020.127509.

3. Chen, O, Riedemann, L, Etoc, F, Herrmann, H, Coppey, M, Barch, M, et al.. Magneto-fluorescent core-shell supernanoparticles. Nat Commun 2014;5:1–8. https://doi.org/10.1038/ncomms6093.

4. Key, J, Leary, JF. Nanoparticles for multimodal in vivo imaging in nanomedicine. Int J Nanomed 2014;9:711. https://doi.org/10.2147/ijn.s53717.

5. Figuerola, A, Di Corato, R, Manna, L, Pellegrino, T. From iron oxide nanoparticles towards advanced iron-based inorganic materials designed for biomedical applications. Pharmacol Res 2010;62:126–43. https://doi.org/10.1016/j.phrs.2009.12.012.

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Infection-Sensitive SPION/PLGA Scaffolds Promote Periodontal Regeneration via Antibacterial Activity and Macrophage-Phenotype Modulation;ACS Applied Materials & Interfaces;2024-08-02

2. Iron scavenging and myeloid cell polarization;Trends in Immunology;2024-08

3. Determining M2 macrophages content for the anti-tumor effects of metal-organic framework-encapsulated pazopanib nanoparticles in breast cancer;Journal of Nanobiotechnology;2024-07-20

4. Transition Metal Oxide Nanomaterials: New Weapons to Boost Anti-Tumor Immunity Cycle;Nanomaterials;2024-06-21

5. Macrophages and microglia in inflammation and neuroinflammation underlying different pain states;Medical Review;2023-10-01