Influence of physicochemical properties of silver nanoparticles on mast cell activation and degranulation

被引:44
作者
Aldossari, Abdullah A. [1 ]
Shannahana, Jonathan H. [1 ]
Podila, Ramakrishna [2 ,3 ,4 ]
Brown, Jared M. [1 ]
机构
[1] Univ Colorado, Skaggs Sch Pharm & Pharmaceut Sci, Dept Pharmaceut Sci, Aurora, CO 80045 USA
[2] Clemson Univ, Dept Phys & Astron, Clemson, SC 29634 USA
[3] Clemson Univ, Clemson Nanomaterials Ctr, Clemson, SC 29625 USA
[4] Clemson Univ, COMSET, Clemson, SC 29625 USA
关键词
Silver nanoparticles; Bone marrow-derived mast cell; Scavenger receptor B1; Lamp2; Osteopontin; HIGH-DENSITY-LIPOPROTEIN; SCAVENGER RECEPTOR BI; IN-VIVO TOXICITY; PARTICLE-SHAPE; ENGINEERED NANOMATERIALS; INFLAMMATORY RESPONSES; OXIDATIVE STRESS; NANO-SILVER; EXPOSURE; CYTOTOXICITY;
D O I
10.1016/j.tiv.2014.10.008
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Silver nanoparticles (AgNPs) are increasingly being incorporated into products for their antimicrobial properties. This has resulted in increased human exposures and the possibility of adverse health effects. Mast cells orchestrate allergic immune responses through degranulation and release of pre-formed mediators. Little data exists on understanding interactions of AgNPs with mast cells and the properties that influence activation and degranulation. Using bone marrow-derived mast cells and AgNPs of varying physicochemical properties we tested the hypothesis that AgNP physicochemical properties influence mast cell degranulation and osteopontin production. AgNPs evaluated included spherical 20 nm and 110 nm suspended in either polyvinylpyrrolidone (PVP) or citrate, Ag plates suspended in PVP of diameters between 40-60 nm or 100-130 nm, and Ag nanowires suspended in PVP with thicknesses <100 nm and length up to 2 mu m. Mast cell responses were found to be dependent on the physicochemical properties of the AgNP. Further, we determined a role for scavenger receptor B1 in AgNP-induced mast cell respons8. Mast cell degranulation was not dependent on AgNP dissolution but was prevented by tyrosine lcinase inhibitor pretreatment. This study suggests that exposure to AgNPs may elicit adverse mast cell responses that could contribute to the initiation or exacerbation of allergic disease. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:195 / 203
页数:9
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