National Institute for Occupational Safety and Health, Morgantown, WV 26505, United States.
Mutat Res. 2012 Jun 14;745(1-2):28-37. doi: 10.1016/j.mrgentox.2011.11.017. Epub 2011 Dec 8.
Carbon nanotubes were among the earliest products of nanotechnology and have many potential applications in medicine, electronics, and manufacturing. The low density, small size, and biological persistence of carbon nanotubes create challenges for exposure control and monitoring and make respiratory exposures to workers likely. We have previously shown mitotic spindle aberrations in cultured primary and immortalized human airway epithelial cells exposed to 24, 48 and 96 μg/cm(2) single-walled carbon nanotubes (SWCNT). To investigate mitotic spindle aberrations at concentrations anticipated in exposed workers, primary and immortalized human airway epithelial cells were exposed to SWCNT for 24-72 h at doses equivalent to 20 weeks of exposure at the Permissible Exposure Limit for particulates not otherwise regulated. We have now demonstrated fragmented centrosomes, disrupted mitotic spindles and aneuploid chromosome number at those doses. The data further demonstrated multipolar mitotic spindles comprised 95% of the disrupted mitoses. The increased multipolar mitotic spindles were associated with an increased number of cells in the G2 phase of mitosis, indicating a mitotic checkpoint response. Nanotubes were observed in association with mitotic spindle microtubules, the centrosomes and condensed chromatin in cells exposed to 0.024, 0.24, 2.4 and 24 μg/cm(2) SWCNT. Three-dimensional reconstructions showed carbon nanotubes within the centrosome structure. The lower doses did not cause cytotoxicity or reduction in colony formation after 24h; however, after three days, significant cytotoxicity was observed in the SWCNT-exposed cells. Colony formation assays showed an increased proliferation seven days after exposure. Our results show significant disruption of the mitotic spindle by SWCNT at occupationally relevant doses. The increased proliferation that was observed in carbon nanotube-exposed cells indicates a greater potential to pass the genetic damage to daughter cells. Disruption of the centrosome is common in many solid tumors including lung cancer. The resulting aneuploidy is an early event in the progression of many cancers, suggesting that it may play a role in both tumorigenesis and tumor progression. These results suggest caution should be used in the handling and processing of carbon nanotubes.
碳纳米管是纳米技术最早的产物之一,在医学、电子和制造领域有许多潜在的应用。碳纳米管的低密度、小尺寸和生物持久性给暴露控制和监测带来了挑战,使工人很可能接触到呼吸暴露。我们之前已经证明,在暴露于 24、48 和 96μg/cm(2)单壁碳纳米管(SWCNT)的培养原代和永生化人呼吸道上皮细胞中出现有丝分裂纺锤体异常。为了研究暴露工人预期浓度下的有丝分裂纺锤体异常,原代和永生化人呼吸道上皮细胞在相当于可允许暴露限值下暴露于 SWCNT 24-72 小时,该限值适用于未被管制的颗粒。我们现在已经证明在这些剂量下,中心体碎片化、有丝分裂纺锤体破坏和非整倍体染色体数目增加。数据进一步表明,多极有丝分裂纺锤体占破坏有丝分裂的 95%。增加的多极有丝分裂纺锤体与有丝分裂 G2 期的细胞数量增加有关,表明存在有丝分裂检查点反应。在暴露于 0.024、0.24、2.4 和 24μg/cm(2)SWCNT 的细胞中,观察到纳米管与有丝分裂纺锤体微管、中心体和浓缩染色质有关。三维重建显示,碳纳米管位于中心体结构内。较低剂量在暴露 24 小时后不会引起细胞毒性或集落形成减少;然而,在三天后,暴露于 SWCNT 的细胞中观察到明显的细胞毒性。集落形成测定显示暴露后七天增殖增加。我们的结果表明,SWCNT 在职业相关剂量下显著破坏有丝分裂纺锤体。在暴露于碳纳米管的细胞中观察到的增殖增加表明,将遗传损伤传递给子细胞的可能性更大。中心体的破坏在包括肺癌在内的许多实体瘤中很常见。由此产生的非整倍体是许多癌症进展的早期事件,表明它可能在肿瘤发生和肿瘤进展中都发挥作用。这些结果表明,在处理和加工碳纳米管时应谨慎。