Aldossari Abdullah A, Shannahan Jonathan H, Podila Ramakrishna, Brown Jared M
Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Toxicol In Vitro. 2015 Feb;29(1):195-203. doi: 10.1016/j.tiv.2014.10.008.
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 μm. 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 responses. Mast cell degranulation was not dependent on AgNP dissolution but was prevented by tyrosine kinase 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.
银纳米颗粒(AgNPs)因其抗菌特性正越来越多地被添加到产品中。这导致人类接触增加以及产生不良健康影响的可能性。肥大细胞通过脱颗粒和释放预先形成的介质来协调过敏免疫反应。关于了解AgNPs与肥大细胞的相互作用以及影响激活和脱颗粒的特性的数据很少。我们使用骨髓来源的肥大细胞和具有不同物理化学性质的AgNPs,测试了AgNP物理化学性质影响肥大细胞脱颗粒和骨桥蛋白产生的假设。评估的AgNPs包括悬浮在聚乙烯吡咯烷酮(PVP)或柠檬酸盐中的20 nm和110 nm球形颗粒、悬浮在PVP中的直径在40 - 60 nm或100 - 130 nm之间的银片,以及悬浮在PVP中的厚度小于100 nm且长度达2μm的银纳米线。发现肥大细胞反应取决于AgNP的物理化学性质。此外,我们确定了清道夫受体B1在AgNP诱导的肥大细胞反应中的作用。肥大细胞脱颗粒不依赖于AgNP溶解,但酪氨酸激酶抑制剂预处理可阻止其发生。这项研究表明,接触AgNPs可能引发不良的肥大细胞反应,这可能导致过敏性疾病的起始或加重。