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静脉注射聚乙烯亚胺修饰的氧化铁纳米颗粒对免疫应激小鼠中NF-κB蛋白表达的影响

Intravenous Injection of PEI-Decorated Iron Oxide Nanoparticles Impacts NF-kappaB Protein Expression in Immunologically Stressed Mice.

作者信息

Schwarz Claudia, Göring Julia, Grüttner Cordula, Hilger Ingrid

机构信息

Experimental Radiology, Institute of Diagnostic and Interventional Radiology, Jena University Hospital, Friedrich Schiller University Jena, Am Klinikum 1, D-07740 Jena, Germany.

Micromod Partikeltechnologie GmbH, Schillingallee 68, D-18057 Rostock, Germany.

出版信息

Nanomaterials (Basel). 2023 Dec 18;13(24):3166. doi: 10.3390/nano13243166.


DOI:10.3390/nano13243166
PMID:38133063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10745731/
Abstract

Nanoparticle-based formulations are considered valuable tools for diagnostic and treatment purposes. The surface decoration of nanoparticles with polyethyleneimine (PEI) is often used to enhance their targeting and functional properties. Here, we aimed at addressing the long-term fate and the potential "off-target" effects of PEI decorated iron oxide nanoparticles (PEI-MNPs) in individuals with low-grade and persistent systemic inflammation. For this purpose, we synthesized PEI-MNPs (core-shell method, PEI coating under high pressure homogenization). Further on, we induced a low-grade and persistent inflammation in mice through regular subcutaneous injection of pathogen-associated molecular patterns (PAMPs, from zymosan). PEI-MNPs were injected intravenously. Up to 7 weeks thereafter, the blood parameters were determined via automated fluorescence flow cytometry, animals were euthanized, and the organs analyzed for iron contents (atomic absorption spectrometry) and for expression of NF-κB associated proteins (p65, IκBα, p105/50, p100/52, COX-2, Bcl-2, SDS-PAGE and Western blotting). We observed that the PEI-MNPs had a diameter of 136 nm and a zeta-potential 56.9 mV. After injection in mice, the blood parameters were modified and the iron levels were increased in different organs. Moreover, the liver of animals showed an increased protein expression of canonical NF-κB signaling pathway members early after PEI-MNP application, whereas at the later post-observation time, members of the non-canonical signaling pathway were prominent. We conclude that the synergistic effect between PEI-MNPs and the low-grade and persistent inflammatory state is mainly due to the hepatocytes sensing infection (PAMPs), to immune responses resulting from the intracellular metabolism of the uptaken PEI-MNPs, or to hepatocyte and immune cell communications. Therefore, we suggest a careful assessment of the safety and toxicity of PEI-MNP-based carriers for gene therapy, chemotherapy, and other medical applications not only in healthy individuals but also in those suffering from chronic inflammation.

摘要

基于纳米颗粒的制剂被认为是用于诊断和治疗目的的有价值工具。用聚乙烯亚胺(PEI)对纳米颗粒进行表面修饰常用于增强其靶向性和功能特性。在此,我们旨在探讨PEI修饰的氧化铁纳米颗粒(PEI-MNPs)在低度和持续性全身炎症个体中的长期归宿及潜在的“脱靶”效应。为此,我们合成了PEI-MNPs(核壳法,高压匀浆下进行PEI包被)。进一步地,我们通过定期皮下注射病原体相关分子模式(PAMPs,来自酵母聚糖)在小鼠中诱导低度和持续性炎症。静脉注射PEI-MNPs。此后长达7周,通过自动荧光流式细胞术测定血液参数,对动物实施安乐死,并分析器官中的铁含量(原子吸收光谱法)以及NF-κB相关蛋白(p65、IκBα、p105/50、p100/52、COX-2、Bcl-2)的表达(SDS-PAGE和蛋白质免疫印迹法)。我们观察到PEI-MNPs的直径为136 nm,zeta电位为56.9 mV。在小鼠体内注射后,血液参数发生改变,不同器官中的铁水平升高。此外,在应用PEI-MNPs后早期,动物肝脏中经典NF-κB信号通路成员的蛋白表达增加,而在观察后期,非经典信号通路成员占主导。我们得出结论,PEI-MNPs与低度和持续性炎症状态之间的协同效应主要归因于肝细胞感知感染(PAMPs)、摄取的PEI-MNPs细胞内代谢引发的免疫反应,或肝细胞与免疫细胞之间的通讯。因此,我们建议不仅要在健康个体中,而且要在患有慢性炎症的个体中仔细评估基于PEI-MNP的载体用于基因治疗、化疗及其他医学应用时的安全性和毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/8f672077d204/nanomaterials-13-03166-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/48e4ae4dc5d5/nanomaterials-13-03166-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/c68bc49997c0/nanomaterials-13-03166-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/d8da20ac953d/nanomaterials-13-03166-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/98c98867f57b/nanomaterials-13-03166-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/7a6f0c652196/nanomaterials-13-03166-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/6a7ce85d99a9/nanomaterials-13-03166-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/8f672077d204/nanomaterials-13-03166-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/48e4ae4dc5d5/nanomaterials-13-03166-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/c68bc49997c0/nanomaterials-13-03166-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/d8da20ac953d/nanomaterials-13-03166-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/98c98867f57b/nanomaterials-13-03166-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/7a6f0c652196/nanomaterials-13-03166-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/6a7ce85d99a9/nanomaterials-13-03166-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef74/10745731/8f672077d204/nanomaterials-13-03166-g007.jpg

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