Tsai Tsen-Ni, Lee Tzu-Ying, Liu Maw-Shung, Ho Jia-Jing, Huang Li-Ju, Liu Chia-Jen, Chen Tsan-Ju, Yang Rei-Cheng
Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;
Teaching and Research Center, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan;
Am J Physiol Cell Physiol. 2015 Jun 15;308(12):C959-63. doi: 10.1152/ajpcell.00044.2015. Epub 2015 Apr 15.
Silver nanoparticles (Ag-nps) have been widely used in various biomedical products. Compared with its hazardous effects extensively being studied, rare attention has been paid to the potential protective effect of Ag-nps to human health. The present study was designed to evaluate the protective effects of Ag-nps and heat shock treatment on tumor necrosis factor-α (TNF-α)-induced cell damage in Clone 9 cells. Clone 9 cells were pretreated with nonlethal concentration of Ag-nps (1 μg/ml) or heat shock, and then cell damages were induced by TNF-α (1 ng/ml). Protective effects of Ag-nps administration or heat shock treatment were determined by examining the TNF-α-induced changes in cell viabilities. The results showed that the intensity of cytotoxicity produced by TNF-α was alleviated upon treatment with nonlethal concentration of Ag-nps (1 μg/ml). Similar protective effects were also found upon heat shock treatment. These data demonstrate that Ag-nps and heat shock treatment were equally capable of inducing heat shock protein 70 (HSP70) protein expression in Clone 9 cells. The results suggest that clinically Ag-nps administration is a viable strategy to induce endogenous HSP70 expression instead of applying heat shock. In conclusion, our study for the first time provides evidence that Ag-nps may act as a viable alternative for HSP70 induction clinically.
银纳米颗粒(Ag-nps)已广泛应用于各种生物医学产品中。与其受到广泛研究的有害影响相比,人们对Ag-nps对人类健康的潜在保护作用关注较少。本研究旨在评估Ag-nps和热休克处理对肿瘤坏死因子-α(TNF-α)诱导的Clone 9细胞损伤的保护作用。用非致死浓度的Ag-nps(1μg/ml)或热休克预处理Clone 9细胞,然后用TNF-α(1ng/ml)诱导细胞损伤。通过检测TNF-α诱导的细胞活力变化来确定Ag-nps给药或热休克处理的保护作用。结果表明,用非致死浓度的Ag-nps(1μg/ml)处理后,TNF-α产生的细胞毒性强度有所减轻。热休克处理也发现了类似的保护作用。这些数据表明,Ag-nps和热休克处理同样能够在Clone 9细胞中诱导热休克蛋白70(HSP70)的蛋白表达。结果表明,临床上给予Ag-nps是诱导内源性HSP70表达的可行策略,而不是应用热休克。总之,我们的研究首次提供了证据,表明Ag-nps在临床上可能是诱导HSP70的可行替代方法。