The genotoxic effects in the leukocytes of workers handling nanocomposite materials

Mutagenesis. 2020 Sep 12;35(4):331-340. doi: 10.1093/mutage/geaa016.

Abstract

The extensive development of nanotechnologies and nanomaterials poses a number of questions to toxicologists about the potential health risks of exposure to nanoparticles (NP). In this study, we analysed DNA damage in the leukocytes of 20 workers who were long-term exposed (18 ± 10 years) to NP in their working environment. Blood samples were collected in September 2016, before and after a shift, to assess (i) the chronic effects of NP on DNA (pre-shift samples) and (ii) the acute effects of exposure during the shift (the difference between pre- and post-shift samples). The samples from matched controls were taken in parallel with workers before the shift. Leukocytes were isolated from heparinised blood on a Ficoll gradient. The enzyme-modified comet assay (DNA formamido-pyrimidine-glycosylase and endonuclease III) demonstrated a considerable increase of both single- and double-strand breaks in DNA (DNA-SB) and oxidised bases when compared with the controls (2.4× and 2×, respectively). Acute exposure induced a further increase of DNA-SB. The welding and smelting of nanocomposites represented a higher genotoxic risk than milling and grinding of nanocomposite surfaces. Obesity appeared to be a factor contributing to an increased risk of oxidative damage to DNA. The data also indicated a higher susceptibility of males vs. females to NP exposure. The study was repeated in September 2017. The results exhibited similar trend, but the levels of DNA damage in the exposed subjects were lower compared to previous year. This was probably associated with lower exposure to NP in consequence of changes in nanomaterial composition and working operations. The further study involving also monitoring of personal exposures to NP is necessary to identify (i) the main aerosol components responsible for genotoxic effects in workers handling nanocomposites and (ii) the primary cause of gender differences in response to NP action.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Comet Assay
  • DNA / drug effects
  • DNA / metabolism
  • DNA Damage*
  • DNA-Formamidopyrimidine Glycosylase
  • Deoxyribonuclease (Pyrimidine Dimer)
  • Escherichia coli Proteins
  • Female
  • Humans
  • Leukocytes / drug effects*
  • Leukocytes / metabolism
  • Male
  • Middle Aged
  • Mutagens
  • Nanocomposites / toxicity*
  • Occupational Exposure / adverse effects*
  • Oxidative Stress
  • Sex Factors
  • Young Adult

Substances

  • Escherichia coli Proteins
  • Mutagens
  • DNA
  • Deoxyribonuclease (Pyrimidine Dimer)
  • NTH protein, E coli
  • DNA-Formamidopyrimidine Glycosylase