Department of Regulatory Toxicology, National Institute of Pharmaceutical Education & Research (NIPER), Balanagar, Hyderabad, Telangana-500037, India.
Department of Chemical Engineering, Sri Venkateswara College of Engineering, Sriperumbudur, Tamilnadu-602117, India.
Nanomedicine (Lond). 2019 Aug;14(15):1991-2010. doi: 10.2217/nnm-2018-0397. Epub 2019 Jul 29.
Selenium nanoparticles (SeNPs) may have a potential role in treating dermal disorders due to its wide therapeutic properties, but there is a need to evaluate its toxicity in keratinocytes. The present study evaluated the molecular mechanism and mode of cell death induced by SeNPs on dermal keratinocytes. SeNPs were synthesized, characterized and studied in human keratinocytes cells. Oxidative stress and mitochondrial membrane depolarization were evaluated by various techniques. Additionally, autophagy mediated apoptotic cell death was evaluated. SeNPs induced oxidative stress and apoptotic cell death in keratinocytes by increasing autophagy through the formation of acidic lysosomes and autophagosomes. Overall, SeNPs induce the oxidative stress and autophagy mediated apoptotic cell death in human keratinocytes cells.
硒纳米颗粒(SeNPs)由于其广泛的治疗特性,可能在治疗皮肤疾病方面具有潜在作用,但需要评估其对角质细胞的毒性。本研究评估了 SeNPs 对皮肤角质细胞诱导的分子机制和细胞死亡方式。SeNPs 进行了合成、表征,并在人角质细胞中进行了研究。通过各种技术评估了氧化应激和线粒体膜去极化。此外,还评估了自噬介导的细胞凋亡。SeNPs 通过形成酸性溶酶体和自噬体来增加自噬,从而在角质细胞中诱导氧化应激和凋亡性细胞死亡。总的来说,SeNPs 诱导人角质细胞中的氧化应激和自噬介导的凋亡性细胞死亡。