The repeated cytogenetic analysis of subjects occupationally exposed to nanoparticles: a pilot study

Author:

Rossnerova Andrea1,Pelclova Daniela2,Zdimal Vladimir3,Rossner Pavel1,Elzeinova Fatima1,Vrbova Kristyna1,Topinka Jan1,Schwarz Jaroslav3,Ondracek Jakub3,Kostejn Martin3,Komarc Martin4,Vlckova Stepanka2,Fenclova Zdenka2,Dvorackova Stepanka567

Affiliation:

1. Department of Genetic Toxicology and Nanotoxicology, Institute of Experimental Medicine of the Czech Academy of Sciences, Prague, Czech Republic

2. Department of Occupational Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic

3. Laboratory of Aerosol Chemistry and Physics, Institute of Chemical Process Fundamentals of the Czech Academy of Sciences, Prague, Czech Republic

4. Institute of Biophysics and Informatics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic

5. Department of Machining and Assembly, Technical University in Liberec, Liberec, Czech Republic

6. Department of Engineering Technology, Technical University in Liberec, Liberec, Czech Republic

7. Department of Material Science, Technical University in Liberec, Liberec, Czech Republic

Abstract

Abstract The application of nanomaterials has been rapidly increasing during recent years. Inhalation exposure to nanoparticles (NP) may result in negative toxic effects but there is a critical lack of human studies, especially those related to possible DNA alterations. We analyzed pre-shift and post-shift a group of nanocomposite researchers with a long-term working background (17.8 ± 10.0 years) and matched controls. The study group consisted of 73.2% males and 26.8% females. Aerosol exposure monitoring during a working shift (involving welding, smelting, machining) to assess the differences in exposure to particulate matter (PM) including nanosized fractions <25–100 nm, and their chemical analysis, was carried out. A micronucleus assay using Human Pan Centromeric probes, was applied to distinguish between the frequency of centromere positive (CEN+) and centromere negative (CEN−) micronuclei (MN) in the binucleated cells. This approach allowed recognition of the types of chromosomal damage: losses and breaks. The monitoring data revealed differences in the exposure to NP related to individual working processes, and in the chemical composition of nanofraction. The cytogenetic results of this pilot study demonstrated a lack of effect of long-term (years) exposure to NP (total frequency of MN, P = 0.743), although this exposure may be responsible for DNA damage pattern changes (12% increase of chromosomal breaks—clastogenic effect). Moreover, short-term (daily shift) exposure could be a reason for the increase of chromosomal breaks in a subgroup of researchers involved in welding and smelting processes (clastogenic effect, P = 0.037). The gender and/or gender ratio of the study participants was also an important factor for the interpretation of the results. As this type of human study is unique, further research is needed to understand the effects of long-term and short-term exposure to NP.

Funder

Grant Agency of the Czech Republic

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Genetics (clinical),Toxicology,Genetics

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