文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
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
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
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 @ 2025

聚丙烯酸包被的氧化铁纳米颗粒可能是追踪炎性单核细胞的有用工具。

Polyacrylic acid-coated iron oxide nanoparticles could be a useful tool for tracking inflammatory monocytes.

作者信息

Giraldo-Villegas Manuela, Urquijo Jeaneth, Arnache-Olmos Oscar L, Rojas-López Mauricio

机构信息

Grupo de Inmunología Celular e Inmunogenética, Sede de Investigación Universitaria (SIU), Universidad de Antioquia (UDEA), Calle 70 No. 52-21, Medellín, Colombia.

Grupo de Física del Estado Sólido, Sede de Investigación Universitaria (SIU), Universidad de Antioquia (UDEA), Medellín, Colombia.

出版信息

Future Sci OA. 2019 Oct 30;5(10):FSO423. doi: 10.2144/fsoa-2019-0066.


DOI:10.2144/fsoa-2019-0066
PMID:31827892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6900970/
Abstract

AIM: To establish the effect of poly(acrylic acid)-coated iron oxide nanoparticles (PAC-IONs) and later exposure to a magnetic field on the differentiation of mononuclear phagocytes into macrophages. METHODS: By flow cytometry, cell death was evaluated with DIOC6 and PI, Poly (ADP-ribose) Polymerases (PARP) fragmentation, H2AX phosphorylation and TUNEL assay. Cytokines by Cytokine bead array and the intracellular amount of iron by atomic absorption spectrometry. RESULTS: PAC-IONs did not induce apoptosis, modify the cell membrane integrity or alter the mitochondrial membrane potential. They did not affect the cell morphology, the pattern of cytokine accumulation or the activating role of differentiation of mononuclear phagocytes into macrophages on the proliferation of autologous T cells. CONCLUSION: This evidence indicates that the PAC-IONs are safe and biocompatible. Moreover, the selectivity of the PAC-IONs for mononuclear phagocytes, as well as their increased uptake by non-classical monocytes, warrant future research with a view to their use as a contrast agent, a useful tool for in vivo tracking of tissue-infiltrating mononuclear phagocytes.

摘要

目的:确定聚丙烯酸包被的氧化铁纳米颗粒(PAC-IONs)以及随后暴露于磁场对单核吞噬细胞分化为巨噬细胞的影响。 方法:通过流式细胞术,使用DIOC6和PI、聚(ADP-核糖)聚合酶(PARP)片段化、H2AX磷酸化和TUNEL检测来评估细胞死亡。通过细胞因子珠阵列检测细胞因子,并通过原子吸收光谱法检测细胞内铁含量。 结果:PAC-IONs未诱导细胞凋亡、改变细胞膜完整性或改变线粒体膜电位。它们不影响细胞形态、细胞因子积累模式或单核吞噬细胞分化为巨噬细胞对自体T细胞增殖的激活作用。 结论:该证据表明PAC-IONs是安全且具有生物相容性的。此外,PAC-IONs对单核吞噬细胞的选择性以及它们被非经典单核细胞增加摄取的特性,值得未来开展研究以将其用作造影剂,这是一种用于体内追踪组织浸润单核吞噬细胞的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/05602bef4b6b/fsoa-05-423-g9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/3dd7e9c870ec/fsoa-05-423-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/ac0406038abc/fsoa-05-423-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/8159b72ea0fb/fsoa-05-423-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/6f0a122db5d8/fsoa-05-423-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/595f4491b3cb/fsoa-05-423-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/a7d293528245/fsoa-05-423-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/fb24af409828/fsoa-05-423-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/5e9be232bc88/fsoa-05-423-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/05602bef4b6b/fsoa-05-423-g9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/3dd7e9c870ec/fsoa-05-423-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/ac0406038abc/fsoa-05-423-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/8159b72ea0fb/fsoa-05-423-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/6f0a122db5d8/fsoa-05-423-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/595f4491b3cb/fsoa-05-423-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/a7d293528245/fsoa-05-423-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/fb24af409828/fsoa-05-423-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/5e9be232bc88/fsoa-05-423-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5866/6900970/05602bef4b6b/fsoa-05-423-g9.jpg

相似文献

[1]
Polyacrylic acid-coated iron oxide nanoparticles could be a useful tool for tracking inflammatory monocytes.

Future Sci OA. 2019-10-30

[2]
Poly(acrylic acid)-Coated Iron Oxide Nanoparticles interact with mononuclear phagocytes and decrease platelet aggregation.

Cell Immunol. 2019-3-26

[3]
Expression of a monocyte chemotactic cytokine by human mononuclear phagocytes.

J Immunol. 1992-2-1

[4]
Uptake of lactoferrin by mononuclear phagocytes inhibits their ability to form hydroxyl radical and protects them from membrane autoperoxidation.

J Immunol. 1991-12-15

[5]
Impact of Superparamagnetic Iron Oxide Nanoparticles on THP-1 Monocytes and Monocyte-Derived Macrophages.

Front Mol Biosci. 2022-2-4

[6]
Biodistribution of polyacrylic acid-coated iron oxide nanoparticles is associated with proinflammatory activation and liver toxicity.

J Appl Toxicol. 2016-10

[7]
Facilitated monocyte-macrophage uptake and tissue distribution of superparmagnetic iron-oxide nanoparticles.

PLoS One. 2009

[8]
Atomic layer deposition coating of carbon nanotubes with aluminum oxide alters pro-fibrogenic cytokine expression by human mononuclear phagocytes in vitro and reduces lung fibrosis in mice in vivo.

PLoS One. 2014-9-12

[9]
Monocytes and dendritic cells in a hypoxic environment: Spotlights on chemotaxis and migration.

Immunobiology. 2008

[10]
The origin and kinetics of mononuclear phagocytes.

J Exp Med. 1968-9-1

引用本文的文献

[1]
Surface Modification Strategies for Chrysin-Loaded Iron Oxide Nanoparticles to Boost Their Anti-Tumor Efficacy in Human Colon Carcinoma Cells.

J Funct Biomater. 2024-2-13

[2]
Nanoparticles targeting monocytes and macrophages as diagnostic and therapeutic tools for autoimmune diseases.

Heliyon. 2023-9-7

[3]
Polyacrylic Acid Nanoplatforms: Antimicrobial, Tissue Engineering, and Cancer Theranostic Applications.

Polymers (Basel). 2022-3-21

本文引用的文献

[1]
Limited Macrophage Positional Dynamics in Progressing or Regressing Murine Atherosclerotic Plaques-Brief Report.

Arterioscler Thromb Vasc Biol. 2018-8

[2]
Correlation analysis of monocyte subsets and insulin resistance considering fetuin-A involvement in patients with type 2 diabetes.

Clin Transl Med. 2018-3-27

[3]
Cellular Differentiation of Human Monocytes Is Regulated by Time-Dependent Interleukin-4 Signaling and the Transcriptional Regulator NCOR2.

Immunity. 2017-12-19

[4]
Metformin and epothilone A treatment up regulate pro-apoptotic PARP-1, Casp-3 and H2AX genes and decrease of AKT kinase level to control cell death of human hepatocellular carcinoma and ovary adenocarcinoma cells.

Toxicol In Vitro. 2017-11-5

[5]
Perturbations of Monocyte Subsets and Their Association with T Helper Cell Differentiation in Acute and Chronic HIV-1-Infected Patients.

Front Immunol. 2017-3-13

[6]
Cell-Derived Nanoparticles are Endogenous Modulators of Sepsis With Therapeutic Potential.

Shock. 2017-9

[7]
Infiltrating CD16 Are Associated with a Reduction in Peripheral CD14CD16 Monocytes and Severe Forms of Lupus Nephritis.

Autoimmune Dis. 2016

[8]
Chronic Low-Grade Inflammation in Childhood Obesity Is Associated with Decreased IL-10 Expression by Monocyte Subsets.

PLoS One. 2016-12-15

[9]
Modulation of dendritic cell and monocyte subsets in tuberculosis-diabetes co-morbidity upon standard tuberculosis treatment.

Tuberculosis (Edinb). 2016-12

[10]
Bone marrow-derived macrophages distinct from tissue-resident macrophages play a pivotal role in Concanavalin A-induced murine liver injury via CCR9 axis.

Sci Rep. 2016-10-11

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索