Labrador-Rached Claudia J, Browning Rebecca T, Braydich-Stolle Laura K, Comfort Kristen K
Department of Chemical and Materials Engineering, University of Dayton, Dayton, OH 45469, USA.
Molecular Bioeffects Branch, Bioeffects Division, Airmen Systems Directorate, Wright-Patterson Air Force Base, OH 45433, USA.
J Toxicol. 2018 Oct 1;2018:1367801. doi: 10.1155/2018/1367801. eCollection 2018.
Due to their distinctive physicochemical properties, platinum nanoparticles (PtNPs) have emerged as a material of interest for a number of biomedical therapeutics. However, in some instances NP exposure has been correlated to health and safety concerns, including cytotoxicity, activation of cellular stress, and modification to normal cell functionality. As PtNPs have induced differential cellular responses , the goal of this study was to further characterize the behavior and toxicological potential of PtNPs within a HepG2 liver model. This study identified that a high PtNP dosage induced HepG2 cytotoxicity. However, lower, subtoxic PtNP concentrations were able to elicit multiple stress responses, secretion of proinflammatory cytokines, and modulation of insulin-like growth factor-1 dependent signal transduction. Taken together, this work suggests that PtNPs would not be overtly toxic for acute exposures, but sustained cellular interactions might produce long term health consequences.
由于其独特的物理化学性质,铂纳米颗粒(PtNPs)已成为多种生物医学治疗方法中备受关注的材料。然而,在某些情况下,纳米颗粒暴露与健康和安全问题相关,包括细胞毒性、细胞应激激活以及正常细胞功能的改变。由于PtNPs会引发不同的细胞反应,本研究的目的是进一步表征PtNPs在HepG2肝脏模型中的行为和毒理学潜力。该研究发现,高剂量的PtNPs会诱导HepG2细胞毒性。然而,较低的、亚毒性的PtNPs浓度能够引发多种应激反应、促炎细胞因子的分泌以及胰岛素样生长因子-1依赖性信号转导的调节。综上所述,这项工作表明,PtNPs对于急性暴露不会有明显毒性,但持续的细胞相互作用可能会产生长期的健康后果。