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二氧化硅纳米颗粒与内皮细胞的相互作用:流动条件下的摄取及其对血小板黏附的影响

Silica Nanoparticle-Endothelial Interaction: Uptake and Effect on Platelet Adhesion under Flow Conditions.

作者信息

Saikia Jiban, Mohammadpour Raziye, Yazdimamaghani Mostafa, Northrup Hannah, Hlady Vladimir, Ghandehari Hamidreza

机构信息

Utah Center for Nanomedicine, Nano Institute of Utah, University of Utah, Salt Lake City, Utah 84112, United States.

Department of Chemistry, Dibrugarh University, Dibrugarh, Assam 786004, India.

出版信息

ACS Appl Bio Mater. 2018 Nov 19;1(5):1620-1627. doi: 10.1021/acsabm.8b00466. Epub 2018 Nov 30.

Abstract

Silica nanoparticles are extensively used in biomedical applications and consumer products. Little is known about the interaction of these NPs with the endothelium and effect on platelet adhesion under flow conditions in circulation. In this study, we investigated the effect of silica nanoparticles on the endothelium and its inflammation, and subsequent adhesion of flowing platelets in vitro. Platelet counts adhered onto the surface of endothelial cells in the presence of nanoparticles increased at both low and high concentrations of nanoparticles. Preincubation of endothelial cells with nanoparticles also increased platelet adhesion. Interestingly, platelet adhesion onto TNF--treated endothelial cells decreased in the presence of nanoparticles at different concentrations as compared with the absence of nanoparticles. We monitored the expression of different endothelial proteins, known to initiate platelet adhesion, in the presence and absence of silica nanoparticles. We found that silica nanoparticles caused changes in the endothelium such as overexpression of PECAM that promoted platelet adhesion to the endothelial cell.

摘要

二氧化硅纳米颗粒广泛应用于生物医学领域和消费品中。对于这些纳米颗粒在循环流动条件下与内皮细胞的相互作用以及对血小板黏附的影响,我们了解甚少。在本研究中,我们在体外研究了二氧化硅纳米颗粒对内皮细胞及其炎症的影响,以及随后流动血小板的黏附情况。在纳米颗粒存在的情况下,无论是低浓度还是高浓度的纳米颗粒,黏附在内皮细胞表面的血小板数量均增加。内皮细胞与纳米颗粒预孵育也增加了血小板黏附。有趣的是,与不存在纳米颗粒相比,在不同浓度纳米颗粒存在的情况下,血小板在经肿瘤坏死因子-α处理的内皮细胞上的黏附减少。我们监测了在存在和不存在二氧化硅纳米颗粒的情况下,已知可引发血小板黏附的不同内皮蛋白的表达。我们发现二氧化硅纳米颗粒导致内皮细胞发生变化,例如促进血小板黏附到内皮细胞的血小板内皮细胞黏附分子(PECAM)的过表达。

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