Department of Life Sciences, University of Trieste, Via L. Giorgeri 7/9, 34127 Trieste, Italy.
Toxicol In Vitro. 2011 Aug;25(5):1053-60. doi: 10.1016/j.tiv.2011.04.005. Epub 2011 Apr 8.
For their antibacterial activity, silver nanoparticles (Ag NPs) are largely used in various commercially available products designed to come in direct contact with the skin. In this study we investigated the effects of Ag NPs on skin using the human-derived keratinocyte HaCaT cell line model. Ag NPs caused a concentration- and time-dependent decrease of cell viability, with IC(50) values of 6.8 ± 1.3 μM (MTT assay) and 12 ± 1.2 μM (SRB assay) after 7 days of contact. A 24h treatment, followed by a 6 day recovery period in Ag NPs-free medium, reduced cell viability with almost the same potency (IC(50)s of 15.3 ± 4.6 and 35 ± 20 μM, MTT and SRB assays, respectively). Under these conditions, no evidence of induction of necrotic events (propidium iodide assay) was found. Apocynin, NADPH-oxidase inhibitor, or N(G)-monomethyl-L-argynine, nitric oxide synthase inhibitor, did not prevent NPs-induced reduction of cell viability. TEM analysis of cells exposed to NPs for 24h revealed alteration of nuclear morphology but only a marginal presence of individual NPs inside the cells. These results demonstrate that on HaCaT keratinocytes a relatively short time of contact with Ag NPs causes a long-lasting inhibition of cell growth, not associated with consistent Ag NPs internalization.
为了发挥其抗菌活性,银纳米粒子(Ag NPs)被广泛应用于各种与皮肤直接接触的商业产品中。本研究以人角质形成细胞 HaCaT 细胞系模型为对象,研究了 Ag NPs 对皮肤的影响。Ag NPs 导致细胞活力呈浓度和时间依赖性下降,与接触 7 天后的 MTT 检测(IC50 值为 6.8 ± 1.3 μM)和 SRB 检测(IC50 值为 12 ± 1.2 μM)相比,细胞活力在接触 24 小时后,在不含 Ag NPs 的培养基中恢复 6 天,IC50 值分别为 15.3 ± 4.6 和 35 ± 20 μM(MTT 和 SRB 检测)。在这些条件下,没有发现诱导坏死事件的证据(碘化丙啶检测)。NADPH 氧化酶抑制剂(apocynin)或一氧化氮合酶抑制剂(N(G)-monomethyl-L-arginine)不能阻止 NPs 诱导的细胞活力降低。TEM 分析显示,暴露于 NPs 24 小时的细胞核形态发生改变,但细胞内只有少量的单个 NPs 存在。这些结果表明,在 HaCaT 角质形成细胞上,与 Ag NPs 接触相对较短的时间会导致细胞生长的长期抑制,而与 Ag NPs 的持续内化无关。