Multi-walled carbon nanotube induced frustrated phagocytosis, cytotoxicity and pro-inflammatory conditions in macrophages are length dependent and greater than that of asbestos

Toxicol In Vitro. 2015 Oct;29(7):1513-28. doi: 10.1016/j.tiv.2015.06.012. Epub 2015 Jun 15.

Abstract

The potential toxicity of carbon nanotubes (CNTs) has been compared to pathogenic fibres such as asbestos. It is important to test this hypothesis to ascertain safe methods for CNT production, handling and disposal. In this study aspects reported to contribute to CNT toxicity were assessed: length, aspect ratio, iron content and crystallinity; with responses compared to industrially produced MWCNTs and toxicologically relevant materials such as asbestos. The impacts of these particles on a range of macrophage models in vitro were assessed due to the key role of macrophages in particle clearance and particle/fibre-induced disease. Industrially produced and long MWCNTs were cytotoxic to cells, and were potent in inducing pro-inflammatory and pro-fibrotic immune responses. Short CNTs did not induce any cytotoxicity. Frustrated phagocytosis was most evident in response to long CNTs, as was respiratory burst and reduction in phagocytic ability. Short CNTs, metal content and crystallinity had less or no influence on these endpoints, suggesting that many responses were fibre-length dependent. This study demonstrates that CNTs are potentially pathogenic, as they were routinely found to induce detrimental responses in macrophages greater than those induced by asbestos at the same mass-based dose.

Keywords: Asbestos; Carbon nanotubes; Frustrated phagocytosis; Nanoparticles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Asbestos, Amosite / toxicity
  • Bronchoalveolar Lavage Fluid / cytology
  • Cell Line
  • Cell Survival / drug effects
  • Cells, Cultured
  • Chemokine CCL2 / metabolism
  • Humans
  • Iron / analysis
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Macrophages / physiology
  • Male
  • Mice
  • Nanotubes, Carbon / chemistry
  • Nanotubes, Carbon / toxicity*
  • Particle Size
  • Phagocytosis / drug effects
  • Rats, Sprague-Dawley
  • Soot / toxicity
  • Transforming Growth Factor beta1 / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Chemokine CCL2
  • Nanotubes, Carbon
  • Soot
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha
  • Asbestos, Amosite
  • Iron