Apoptosis-mediated in vivo toxicity of hydroxylated fullerene nanoparticles in soil nematode Caenorhabditis elegans

Authors
Cha, Yun JeongLee, JaesangChoi, Shin Sik
Issue Date
2012-03
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
CHEMOSPHERE, v.87, no.1, pp.49 - 54
Abstract
Although a number of manufactured nanoparticles are applied for the medical and clinical purposes, the understanding of interaction between nanomaterials and biological systems are still insufficient. Using nematode Caenorhabditis elegans model organism, we here investigated the in vivo toxicity or safety of hydroxylated fullerene nanoparticles known to detoxify anti-cancer drug-induced oxidative damages in mammals. The survival ratio of C. elegans rapidly decreased by the uptake of nanoparticles from their 14 larval stage with resulting in shortened lifespan (20 d). Both reproduction rate and body size of C. elegans were also reduced after exposure to 100 mu g mL(-1) of fullerol. We found ectopic cell corpses caused by apoptotic cell death in the adult worms grown with fullerol nanoparticles. By the mutation of core pro-apoptotic regulator genes, ced-3 and ced-4, these nanoparticle-induced cell death were significantly suppressed, and the viability of animals consequently increased despite of nanoparticle uptake. The apoptosis-mediated toxicity of nanoparticles particularly led to the disorder of digestion system in the animals containing a large number of undigested foods in their intestine. These results demonstrated that the water-soluble fullerol nanoparticles widely used in medicinal applications have a potential for inducing apoptotic cell death in multicellular organisms despite of their antioxidative detoxifying property. (C) 2011 Elsevier Ltd. All rights reserved.
Keywords
LIFE-SPAN; C-60(OH)(24); DOXORUBICIN; NC(60); LIFE-SPAN; C-60(OH)(24); DOXORUBICIN; NC(60); Fullerene; Fullerol; Apoptosis; Toxicity; Nanoparticle; Caenorhabditis elegans
ISSN
0045-6535
URI
https://pubs.kist.re.kr/handle/201004/129494
DOI
10.1016/j.chemosphere.2011.11.054
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KIST Article > 2012
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