Barthel Hélène, Darne Christian, Gaté Laurent, Visvikis Athanase, Seidel Carole
Institut National de Recherche et de Sécurité, CEDEX, F-54519 Vandœuvre-lès-Nancy, France.
Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), Biopôle, Campus Biologie Santé, UMR 7365 CNRS-Université de Lorraine, CEDEX, F-54000 Vandœuvre-lès-Nancy, France.
Nanomaterials (Basel). 2021 Jul 1;11(7):1742. doi: 10.3390/nano11071742.
In the field of nanotechnology, the use of multi-walled carbon nanotubes (MWCNTs) is growing. Pulmonary exposure during their production, use, and handling is raising concerns about their potential adverse health effects. The purpose of this study is to assess how the physical characteristics of MWCNTs, such as diameter and/or length, can play a role in cellular toxicity. Our experimental design is based on the treatment of human bronchial epithelial cells (BEAS-2B) for six weeks with low concentrations (0.125-1 µg/cm) of MWCNTs having opposite characteristics: NM-403 and Mitsui-7. Following treatment with both MWCNTs, we observed an increase in mitotic abnormalities and micronucleus-positive cells. The cytotoxic effect was delayed in cells treated with NM-403 compared to Mitsui-7. After 4-6 weeks of treatment, a clear cellular morphological change from epithelial to fibroblast-like phenotype was noted, together with a change in the cell population composition. BEAS-2B cells underwent a conversion from the epithelial to mesenchymal state as we observed a decrease in the epithelial marker E-cadherin and an increased expression of mesenchymal markers N-cadherin, Vimentin, and Fibronectin. After four weeks of recovery, we showed that the induced epithelial-mesenchymal transition is reversible, and that the degree of reversibility depends on the MWCNT.
在纳米技术领域,多壁碳纳米管(MWCNTs)的应用正在不断增加。在其生产、使用和处理过程中的肺部暴露引发了人们对其潜在健康不良影响的担忧。本研究的目的是评估MWCNTs的物理特性,如直径和/或长度,如何在细胞毒性中发挥作用。我们的实验设计基于用具有相反特性的低浓度(0.125 - 1 µg/cm)MWCNTs(NM - 403和三井 - 7)处理人支气管上皮细胞(BEAS - 2B)六周。在用两种MWCNTs处理后,我们观察到有丝分裂异常和微核阳性细胞增加。与三井 - 7相比,用NM - 403处理的细胞的细胞毒性作用出现延迟。处理4 - 6周后,注意到细胞形态从上皮样明显转变为成纤维细胞样表型,同时细胞群体组成也发生了变化。由于我们观察到上皮标志物E - 钙黏蛋白减少,间充质标志物N - 钙黏蛋白、波形蛋白和纤连蛋白的表达增加,BEAS - 2B细胞经历了从上皮状态到间充质状态的转变。在四周的恢复后,我们表明诱导的上皮 - 间充质转化是可逆的,并且可逆程度取决于MWCNT。