Probing and preventing quantum dot-induced cytotoxicity with multimodal α-lipoic acid in multiple dimensions of the peripheral nervous system

被引:17
作者
Jain, Manasi P. [1 ]
Choi, Angela O. [1 ]
Nebibert, Kevin D. [1 ]
Maysinger, Dusica [1 ]
机构
[1] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ H3G 1Y6, Canada
关键词
3D explanted cultures; alpha-lipoic acid; dorsal root ganglia; glutathione; lipid droplets; nanotoxicity; peripheral nervous system; quantum dots; TELLURIUM-INDUCED NEUROPATHY; SCHWANN-CELLS; UP-REGULATION; NANOPARTICLES; DEMYELINATION; RAT; REGENERATION; ANTIOXIDANT; AUTOPHAGY; SELENIUM;
D O I
10.2217/NNM.09.3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: Toxicity of nanoparticles developed for biomedical applications is extensively debated as no uniform guidelines are available for studying nanomaterial safety, resulting in conflicting data obtained from different cell types. This study demonstrates the varied toxicity of a selected type of nanoparticle, cadmium telluride quantum dots (QDs), in three increasingly complex cell models of the peripheral nervous system. Materials & methods: QD-induced cytotoxicity was assessed via cell viability assays and biomarkers of subcellular damage in PC12 cells and mixed primary dispersed dorsal root ganglia (DRG) cultures. Morphological analysis of neurite outgrowth was used to determine the viability of axotomized DRG explant cultures. Results & discussion: Cadmium telluride QDs and their core metals exert different degrees of toxicity in the three cell models, the primary dispersed DRGs being the most susceptible. alpha-lipoic acid is an effective, multimodal, cytoprotective agent that can act as an antioxidant, metal chelator and QD-surface modifier in these cell systems. Conclusion: Complex multicellular model systems, along with homogenous cell models, should be utilized in standard screening and monitoring procedures for evaluating nanomaterial safety.
引用
收藏
页码:277 / 290
页数:14
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