A systems toxicology approach on the mechanism of uptake and toxicity of MWCNT in Caenorhabditis elegans.

The increased volumes of carbon nanotubes (CNTs) being utilized in industrial and biomedical processes carries with it an increased risk of unintentional release into the environment, requiring a thorough hazard and risk assessment. In this study, the toxicity of pristine and hydroxylated (OH-) multiwall CNTs (MWCNTs) was investigated in the nematode Caenorhabditis elegans using an integrated systems toxicology approach. To gain an insight into the toxic mechanism of MWCNTs, microarray and proteomics were conducted for C. elegans followed by pathway analyses. The results of pathway analyses suggested endocytosis, phagocytosis, oxidative stress and endoplasmic reticulum (ER) stress, as potential mechanisms of uptake and toxicity, which were subsequently investigated using loss-of-function mutants of genes of those pathways. The expression of phagocytosis related genes (i.e. ced-10 and rab-7) were significantly increased upon exposure to OH-MWCNT, concomitantly with the rescued toxicity by loss-of-function mutants of those genes, such as ced-10(n3246) and rab-7(ok511). An increased sensitivity of the hsp-4(gk514) mutant by OH-MWCNT, along with a decreased expression of hsp-4 at both gene and protein level suggests that MWCNTs may affect ER stress response in C. elegans. Collectively, the results implied phagocytosis to be a potential mechanism of uptake of MWCNTs, and ER and oxidative stress as potential mechanisms of toxicity. The integrated systems toxicology approach applied in this study provided a comprehensive insight into the toxic mechanism of MWCNTs in C. elegans, which may eventually be used to develop an "Adverse Outcome Pathway (AOP)", a recently introduced concept as a conceptual framework to link molecular level responses to higher level effects.

Ecotoxicity of bare and coated silver nanoparticles in the aquatic midge, Chironomus riparius.

Although sediment is generally considered to be the major sink for nanomaterials in aquatic environments, few studies have addressed the ecotoxicity of nanomaterials in the presence of sediment. In the present study, the ecotoxicity of silver nanoparticles (AgNPs) with a range of organic coatings was examined in a freshwater sediment-dwelling organism, Chironomus riparius, using acute and chronic ecotoxicity endpoints, including molecular indicators. The toxicity of AgNPs coated with different organic materials, such as polyvinylpyrrolidone, gum arabic, and citrate, to C. riparius was compared with that of bare-AgNPs and AgNO3 (ionic silver). Total silver concentration was also measured to monitor the behavior of the AgNPs in water and sediment and to determine how ion dissolution affects the toxicity of all AgNPs. The coated- and bare-AgNPs caused DNA damage and oxidative stress-related gene expression. In addition, the bare-AgNPs and AgNO3 had a significant effect on development and reproduction. The surface coatings generally mitigated the toxicity of AgNPs to C. riparius, which can be explained by the reduced number of ions released from coated-AgNPs. Citrate-AgNPs caused the most significant alteration at the molecular level, but this did not translate to higher-level effects. Finally, comparing previously conducted studies on AgNP-induced gene expression without sediments, the authors show that the presence of sediment appears to mitigate the toxicity of AgNPs.

Potential toxicity of differential functionalized multiwalled carbon nanotubes (MWCNT) in human cell line (BEAS2B) and Caenorhabditis elegans.

The aim of this study was to evaluate in vitro (human bronchial epithelial cells, BEAS2B cells) and in vivo (the nematode Caenorhabditis elegans, C. elegans) toxicity outcomes following exposure to pristine as well as surface-functionalized multiwalled carbon nanotubes (MWCNT) following hydroxylation-oxygenation (O(+)), amination (NH2), or carboxylation (COOH) of the carbon nanotubes (CNT). Cell viability and proliferation were measured by Ez-Cytox, trypan blue exclusion, and colony formation assays. The genotoxic potential of the MWCNT was determined by using the alkaline comet assay. In addition, survival and reproduction were used as endpoints for detection of toxicity of MWCNT in C. elegans. The carboxylated (COOH)-MWCNT was found most toxic as evidenced by cytotoxic and genotoxic among all tested compounds. The order of sensitivity was COOH > O(+) > NH2 > pristine. There were almost no marked changes in survival following exposure of C. elegans to MWCNT. It is of interest that only pristine MWCNT exerted significant reduction in reproductive capacity of C. elegans. Surface functionalization significantly influenced the bioactivity of MWCNT, which displayed species as well as target-organ specificity. The mechanisms underlying these specific modes of nano-biological interactions need to be elucidated.

Exposure to zinc oxide nanoparticles affects reproductive development and biodistribution in offspring rats.

Understanding reproductive development effects and transferable properties to next generation of zinc oxide nanoparticles is necessary for prevention of its potential risks. To accomplish this, rats were exposed to zinc oxide nanomaterials (500 mg/kg bw) of less than 100 nm beginning 2 weeks before mating to postnatal day 4. In addition, body distribution of zinc concentration was evaluated in dams and offspring. Rat treated with nano-zinc oxide showed reduced number of born/live pups, decreased body weights of pups and increased fetal resorption. Zinc oxide nanomaterials were also distributed to organs such as mammary tissue of dams and liver and kidney of pups. These results indicate that zinc oxide nanoparticles-exposure before and during pregnancy and lactation could pose health risks to pregnant women and their fetus.