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Original Article

Size dependent toxicity of zinc oxide nano-particles in soil nematode Caenorhabditis elegans

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Pages 423-432 | Received 23 Jan 2014, Accepted 19 Jun 2014, Published online: 22 Jul 2014
 

Abstract

Zinc oxide nano-particles (ZnO NPs), with their unique physico-chemical properties conferred by various size formulations, are extensively used in consumer products. The enormous usage coupled with their release to the environment demands risk assessment of ZnO NPs on health and the environment. Toxicity of ZnO NPs is well understood in comparison to the bulk ZnO. However, toxicity in relation to the NP size is poorly understood. In this context, we examined the adverse effects of different sizes (35 nm, 50 nm and 100 nm) of ZnO NPs in soil nematode C. elegans along with bulk ZnO and ZnCl2. Here, we show that growth, reproduction and behavior of worms were adversely affected by ZnO NPs in a size dependent manner. Further, exposure to ZnO NPs caused modulation of expression/function of genes associated with Insulin/IGF-like signaling pathway and/or stress response pathway in a size dependent manner in exposed worms. The expression of pro-apoptotic gene and suppression of anti-apoptotic genes, together with increased numbers of cell corpses in the germ line, indicated that apoptosis was also dependent on the size of the ZnO NP. Taken together, our study provides evidence that exposure to ZnO NPs disrupts various physiological processes and causes apoptosis in the germ-line even at very low concentration in a size dependent manner. Our finding suggests the inclusion of size as an additional measure for the cautious monitoring of ZnO NP disposal into the environment.

Acknowledgements

We thank Drs. Chauhan LKS, Saxena PN CSIR-IITR for carrying out the TEM and SEM-EDAX of nanoparticles. We are grateful to Dr. Subramanium K, IIT-Kanpur, India for providing the C. elegans N2 strain and OP50 stocks, to Prof. Zhou Z, Baylor College of Medicine, Houston, Texas for providing us ZH814 strain, to Dr. Pomerai D, University of Nottingham, UK for the GFP transgenic strains of C. elegans employed in the present study. We thank Mr. Lalit PC, CSIR-IITR and Mr. Anshuman S, CSIR-IITR for their help during real-time and enzyme assays. The funding of Council of Scientific and Industrial Research, New Delhi through network project (BSC0112) to AS and research fellowships to PK, MS and fellowship from University Grants Commission, New Delhi to YN is gratefully acknowledged.

Declaration of interest

The authors declare no competing financial interests.

Supplementary material available online

Supplementary Figures S1–S7 and Tables S1 and S2.

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