Cytotoxicity profiles of multi-walled carbon nanotubes with different physico-chemical properties

Toxicol Mech Methods. 2020 Sep;30(7):477-489. doi: 10.1080/15376516.2020.1761920. Epub 2020 May 22.

Abstract

Multi-walled carbon nanotubes (MWCNTs) have industrial applications in the nanotechnology field. The physico-chemical properties of MWCNTs vary greatly depending on MWCNT manufacture and application. It has been pointed out that their needle shape and high durability are important factors that determine the biopersistence of fibers and can lead to inhalation toxicity or cytotoxicity. In this study, we prepared six suspensions of MWCNTs differing in diameter and length, and performed in vitro cell-based assays for 24 h using NR8383 rat alveolar macrophages. Rigid, needle-shaped MWCNTs with a large diameter (>50 µm) penetrated the cytoplasm and decreased cell survival without generating intracellular reactive oxygen species (ROS), significantly up-regulated many genes involved in inflammatory responses, response to oxidative stress and apoptosis, and extracellular matrix degradation. Bent MWCNTs with a small diameter (<20 µm) were phagocytosed in vacuole-like cellular compartments and decreased cell survival along with intracellular ROS generation. Straight, thin MWCNTs with a small diameter (<20 µm) caused a slight intracellular ROS generation but no decrease in cell viability. Some straight, long, and thin MWCNTs were found in the mitochondria and near the nuclei; however, no mutagenesis was observed. The in vitro cell-based assays showed high cytotoxicity of MWCNTs with a large diameter (>50 µm), moderate and low cytotoxicity of MWCNTs with a small diameter (<20 µm). These results suggested that the diameter of MWCNTs considerably contributes to their cytotoxicity.

Keywords: Multi-walled carbon nanotubes; cytotoxicity; gene expression profiles; macrophages; nanomaterials.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Cell Line
  • Cell Survival / drug effects
  • Cytokines / genetics
  • Cytokines / metabolism
  • Inflammation Mediators / metabolism
  • Macrophages, Alveolar / drug effects*
  • Macrophages, Alveolar / metabolism
  • Macrophages, Alveolar / ultrastructure
  • Nanotubes, Carbon / toxicity*
  • Oxidative Stress / drug effects
  • Particle Size
  • Phagocytosis*
  • Rats
  • Reactive Oxygen Species / metabolism
  • Transcriptome

Substances

  • Cytokines
  • Inflammation Mediators
  • Nanotubes, Carbon
  • Reactive Oxygen Species