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对暴露于银纳米颗粒的人类免疫细胞免疫调节反应的质谱流式细胞术研究

Mass Cytometry Exploration of Immunomodulatory Responses of Human Immune Cells Exposed to Silver Nanoparticles.

作者信息

Bae Jiwon, Ha My, Perumalsamy Haribalan, Lee Yangsoon, Song Jaewoo, Yoon Tae-Hyun

机构信息

Department of Chemistry, College of Natural Sciences, Hanyang University, Seoul 04763, Korea.

Research Institute for Convergence of Basic Science, Hanyang University, Seoul 04763, Korea.

出版信息

Pharmaceutics. 2022 Mar 12;14(3):630. doi: 10.3390/pharmaceutics14030630.

DOI:10.3390/pharmaceutics14030630
PMID:35336005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8954471/
Abstract

Increasing production and application of silver nanoparticles (Ag NPs) have raised concerns on their possible adverse effects on human health. However, a comprehensive understanding of their effects on biological systems, especially immunomodulatory responses involving various immune cell types and biomolecules (e.g., cytokines and chemokines), is still incomplete. In this study, a single-cell-based, high-dimensional mass cytometry approach is used to investigate the immunomodulatory responses of Ag NPs using human peripheral blood mononuclear cells (hPBMCs) exposed to poly-vinyl-pyrrolidone (PVP)-coated Ag NPs of different core sizes (i.e., 10-, 20-, and 40-nm). Although there were no severe cytotoxic effects observed, Ag and Ag were excessively found in monocytes and dendritic cells, while Ag displayed more affinity with B cells and natural killer cells, thereby triggering the release of proinflammatory cytokines such as IL-2, IL-17A, IL-17F, MIP1β, TNFα, and IFNγ. Our findings indicate that under the exposure conditions tested in this study, Ag NPs only triggered the inflammatory responses in a size-dependent manner rather than induce cytotoxicity in hPBMCs. Our study provides an appropriate ex vivo model to better understand the human immune responses against Ag NP at a single-cell level, which can contribute to the development of targeted drug delivery, vaccine developments, and cancer radiotherapy treatments.

摘要

银纳米颗粒(Ag NPs)产量和应用的不断增加引发了人们对其可能对人类健康产生的不利影响的担忧。然而,对于它们对生物系统的影响,尤其是涉及各种免疫细胞类型和生物分子(如细胞因子和趋化因子)的免疫调节反应,仍缺乏全面的了解。在本研究中,我们使用基于单细胞的高维质谱流式细胞术方法,以暴露于不同核心尺寸(即10纳米、20纳米和40纳米)的聚乙烯吡咯烷酮(PVP)包覆的Ag NPs的人外周血单个核细胞(hPBMCs)为研究对象,来探究Ag NPs的免疫调节反应。尽管未观察到严重的细胞毒性作用,但在单核细胞和树突状细胞中发现了过量的Ag和Ag,而Ag与B细胞和自然杀伤细胞表现出更高的亲和力,从而触发了促炎细胞因子如IL-2、IL-17A、IL-17F、MIP1β、TNFα和IFNγ的释放。我们的研究结果表明,在本研究测试的暴露条件下,Ag NPs仅以尺寸依赖的方式触发炎症反应,而不会在hPBMCs中诱导细胞毒性。我们的研究提供了一个合适的体外模型,以在单细胞水平上更好地理解人类针对Ag NPs的免疫反应,这有助于靶向药物递送、疫苗开发和癌症放射治疗的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/0ae761d7e705/pharmaceutics-14-00630-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/58ccbf128b3c/pharmaceutics-14-00630-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/10a111a2f984/pharmaceutics-14-00630-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/f6e82a9957d3/pharmaceutics-14-00630-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/999311359172/pharmaceutics-14-00630-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/4398c0956b49/pharmaceutics-14-00630-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/8c8dea6b13b8/pharmaceutics-14-00630-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/0ae761d7e705/pharmaceutics-14-00630-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/58ccbf128b3c/pharmaceutics-14-00630-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/10a111a2f984/pharmaceutics-14-00630-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/f6e82a9957d3/pharmaceutics-14-00630-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/999311359172/pharmaceutics-14-00630-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/4398c0956b49/pharmaceutics-14-00630-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/8c8dea6b13b8/pharmaceutics-14-00630-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b2d/8954471/0ae761d7e705/pharmaceutics-14-00630-g007.jpg

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2
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Plant Cell Environ. 2020 Nov;43(11):2727-2742. doi: 10.1111/pce.13878. Epub 2020 Sep 16.
3
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J Nanobiotechnology. 2024 Mar 17;22(1):118. doi: 10.1186/s12951-024-02364-0.
4
The quest for nanoparticle-powered vaccines in cancer immunotherapy.探索基于纳米颗粒的癌症免疫疗法疫苗。
J Nanobiotechnology. 2024 Feb 14;22(1):61. doi: 10.1186/s12951-024-02311-z.
金纳米颗粒作为一种有效的放射增敏剂:从物理学到患者的跨学科方法。
Cancers (Basel). 2020 Jul 23;12(8):2021. doi: 10.3390/cancers12082021.
4
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5
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