Literature DB >> 19630433

Ultrafine NiO particles induce cytotoxicity in vitro by cellular uptake and subsequent Ni(II) release.

Masanori Horie1, Keiko Nishio, Katsuhide Fujita, Haruhisa Kato, Ayako Nakamura, Shinichi Kinugasa, Shigehisa Endoh, Arisa Miyauchi, Kazuhiro Yamamoto, Hideki Murayama, Etsuo Niki, Hitoshi Iwahashi, Yasukazu Yoshida, Junko Nakanishi.   

Abstract

Nickel oxide (NiO) is one of the important industrial materials used in electronic substrates and for ceramic engineering. Advancements in industrial technology have enabled the manufacture of ultrafine NiO particles. On the other hand, it is well-known that nickel compounds exert toxic effects. The toxicity of nickel compounds is mainly caused by nickel ions (Ni(2+)). However, the ion release properties of ultrafine NiO particles are still unclear. In the present study, the influences of ultrafine NiO particles on cell viability were examined in vitro to obtain fundamental data for the biological effects of ultrafine green NiO and ultrafine black NiO. Ultrafine NiO particles showed higher cytotoxicities toward human keratinocyte HaCaT cells and human lung carcinoma A549 cells than fine NiO particles and also showed higher solubilities in culture medium (Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum) than fine NiO particles. In particular, the concentration of Ni(2+) released into the culture medium by ultrafine green NiO was 150-fold higher than that released by fine green NiO. The concentrations of Ni(2+) released by both types of NiO particles in an aqueous solution containing amino acids were remarkably higher than those released by NiO particles in water. Moreover, we prepared a uniform and stable dispersion of ultrafine black NiO in culture medium and examined its influence on cell viability in comparison with that of NiCl(2), a soluble nickel compound. A medium exchange after 6 h of exposure resulted in a loss of cytotoxicity in the cells exposed to NiCl(2), whereas cytotoxicity was retained in the cells exposed to NiO. Transmission electron microscope observations revealed uptake of both ultrafine and fine NiO particles into HaCaT cells. Taken together, the present results suggest that the intracellular Ni(2+) release could be an important factor that determines the cytotoxicity of NiO. Ultrafine NiO is more cytotoxic than fine NiO in vitro.

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Year:  2009        PMID: 19630433     DOI: 10.1021/tx900171n

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  18 in total

1.  Cross regulation between hypoxia-inducible transcription factor-1α (HIF-1α) and transforming growth factor (TGF)-ß1 mediates nickel oxide nanoparticles (NiONPs)-induced pulmonary fibrosis.

Authors:  Fenghua Qian; Mindi He; Weixia Duan; Lin Mao; Qian Li; Zhengping Yu; Zhou Zhou; Yong Zhang
Journal:  Am J Transl Res       Date:  2015-11-15       Impact factor: 4.060

2.  In vitro acaricidal activity of green synthesized nickel oxide nanoparticles against the camel tick, Hyalomma dromedarii (Ixodidae), and its toxicity on Swiss albino mice.

Authors:  Hoda S M Abdel-Ghany; Sobhy Abdel-Shafy; Mai M Abuowarda; Rabab M El-Khateeb; Essam Hoballah; Abdel Mohsen M Hammam; Magdy M Fahmy
Journal:  Exp Appl Acarol       Date:  2021-03-13       Impact factor: 2.132

Review 3.  Elucidating the mechanisms of nickel compound uptake: a review of particulate and nano-nickel endocytosis and toxicity.

Authors:  Alexandra Muñoz; Max Costa
Journal:  Toxicol Appl Pharmacol       Date:  2011-12-21       Impact factor: 4.219

4.  Intracellular accumulation of indium ions released from nanoparticles induces oxidative stress, proinflammatory response and DNA damage.

Authors:  Yosuke Tabei; Akinari Sonoda; Yoshihiro Nakajima; Vasudevanpillai Biju; Yoji Makita; Yasukazu Yoshida; Masanori Horie
Journal:  J Biochem       Date:  2015-09-15       Impact factor: 3.387

5.  Bioavailability, intracellular mobilization of nickel, and HIF-1α activation in human lung epithelial cells exposed to metallic nickel and nickel oxide nanoparticles.

Authors:  Jodie R Pietruska; Xinyuan Liu; Ashley Smith; Kevin McNeil; Paula Weston; Anatoly Zhitkovich; Robert Hurt; Agnes B Kane
Journal:  Toxicol Sci       Date:  2011-08-09       Impact factor: 4.849

6.  Intracellular accumulation dynamics and fate of zinc ions in alveolar epithelial cells exposed to airborne ZnO nanoparticles at the air-liquid interface.

Authors:  Cosmin Mihai; William B Chrisler; Yumei Xie; Dehong Hu; Craig J Szymanski; Ana Tolic; Jessica A Klein; Jordan N Smith; Barbara J Tarasevich; Galya Orr
Journal:  Nanotoxicology       Date:  2013-12-02       Impact factor: 5.913

7.  Cytotoxicity and ion release of alloy nanoparticles.

Authors:  Anne Hahn; Jutta Fuhlrott; Anneke Loos; Stephan Barcikowski
Journal:  J Nanopart Res       Date:  2012-01-12       Impact factor: 2.253

8.  Long-term (30 days) toxicity of NiO nanoparticles for adult zebrafish Danio rerio.

Authors:  Jevgenij A Kovrižnych; Ružena Sotníková; Dagmar Zeljenková; Eva Rollerová; Elena Szabová
Journal:  Interdiscip Toxicol       Date:  2014-07-16

Review 9.  Evaluation of the effect of time on the distribution of zinc oxide nanoparticles in tissues of rats and mice: a systematic review.

Authors:  Aijie Chen; Xiaoli Feng; Ting Sun; Yanli Zhang; Shengli An; Longquan Shao
Journal:  IET Nanobiotechnol       Date:  2016-06       Impact factor: 1.847

Review 10.  Review and Evaluation of the Potential Health Effects of Oxidic Nickel Nanoparticles.

Authors:  Sharlee L More; Michael Kovochich; Tara Lyons-Darden; Michael Taylor; Alexandra M Schulte; Amy K Madl
Journal:  Nanomaterials (Basel)       Date:  2021-03-05       Impact factor: 5.076

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