Eldawud Reem, Wagner Alixandra, Dong Chenbo, Stueckle Todd A, Rojanasakul Yon, Dinu Cerasela Zoica
Department of Chemical and Biomedical Engineering, West Virginia University, Morgantown, WV 26506, USA.
Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV 26505, USA.
NanoImpact. 2018 Jan;9:72-84. doi: 10.1016/j.impact.2017.10.006. Epub 2017 Oct 28.
The unique properties of single walled carbon nanotubes (SWCNTs) make them viable candidates for versatile implementation in the next generation of biomedical devices for targeted delivery of chemotherapeutic agents or cellular-sensing probes. Such implementation requires user-tailored changes in SWCNT's physicochemical characteristics to allow for efficient cellular integration while maintaining nanotubes' functionality. However, isolated reports showed that user-tailoring could induce deleterious effects in exposed cells, from decrease in cellular proliferation, to changes in cellular adhesion, generation of reactive oxygen species or phenotypical variations, just to name a few. Before full implementation of SWCNTs is achieved, their toxicological profiles need to be mechanistically correlated with their physicochemical properties to determine how the induced cellular fate is related to the exposure conditions or samples' characteristics. Our study provides a comprehensive analysis of the synergistic cyto- and genotoxic effects resulted from short-term exposure of human lung epithelial cells to pristine (as manufactured) and user-tailored SWCNTs, as a function of their physicochemical properties. Specifically, through a systematic approach we are correlating the nanotube uptake and nanotube-induced cellular changes to the sample's physicochemical characteristics (e.g., metal impurities, length, agglomerate size, surface area, dispersion, and surface functionalization). By identifying changes in active hallmarks involved in cell-cell connections and maintaining epithelial layer integrity, we also determine the role that short-term exposure to SWCNTs plays in the overall cellular fate and cellular transformation. Lastly, we assess cellular structure-function relationships to identify non-apoptotic pathways induced by SWCNTs exposure that could however lead to changes in cellular behavior and cellular transformation. Our results show that the degree of cell transformation is a function of the physicochemical properties of the SWCNT, with the nanotube with higher length, higher metal content and larger agglomerate size reducing cell viability to a larger extent. Such changes in cell viability are also complemented by changes in cell structure, cycle and cell-cell interactions, all responsible for maintaining cell fate.
单壁碳纳米管(SWCNTs)的独特性质使其成为下一代生物医学设备中通用应用的可行候选材料,可用于化疗药物的靶向递送或细胞传感探针。这种应用需要对SWCNT的物理化学特性进行用户定制的改变,以实现高效的细胞整合,同时保持纳米管的功能。然而,个别报告显示,用户定制可能会在暴露的细胞中诱导有害影响,从细胞增殖减少到细胞粘附变化、活性氧的产生或表型变异等等。在全面实现SWCNTs的应用之前,需要将它们的毒理学特征与物理化学性质进行机制关联,以确定诱导的细胞命运与暴露条件或样品特性之间的关系。我们的研究全面分析了人类肺上皮细胞短期暴露于原始(制造时)和用户定制的SWCNTs所产生的协同细胞毒性和遗传毒性效应,这是其物理化学性质的函数。具体而言,通过系统方法,我们将纳米管摄取和纳米管诱导的细胞变化与样品的物理化学特性(例如金属杂质、长度、团聚体大小、表面积、分散性和表面功能化)相关联。通过识别参与细胞间连接并维持上皮层完整性的活性标志物的变化,我们还确定了短期暴露于SWCNTs在整体细胞命运和细胞转化中所起的作用。最后,我们评估细胞结构 - 功能关系,以识别SWCNTs暴露诱导的非凋亡途径,这些途径可能导致细胞行为和细胞转化的变化。我们的结果表明,细胞转化程度是SWCNT物理化学性质的函数,长度更长、金属含量更高和团聚体尺寸更大的纳米管在更大程度上降低细胞活力。细胞活力的这种变化还伴随着细胞结构、周期和细胞间相互作用的变化,所有这些都负责维持细胞命运。