The Toxicity of Nanoparticles Depends on Multiple Molecular and Physicochemical Mechanisms

被引:277
作者
Huang, Yue-Wern [1 ]
Cambre, Melissa [1 ]
Lee, Han-Jung [2 ]
机构
[1] Missouri Univ Sci & Technol, Dept Biol Sci, 143 Schrenk Hall,1870 Miner Circle, Rolla, MO 65409 USA
[2] Natl Dong Hwa Univ, Dept Nat Resources & Environm Studies, Hualien 97401, Taiwan
关键词
nanoparticle; toxicity; physicochemical property; cell proliferation; calcium homeostasis; oxidative stress; LUNG EPITHELIAL-CELLS; ZINC-OXIDE NANOPARTICLES; TITANIUM-DIOXIDE NANOPARTICLES; MESENCHYMAL STEM-CELLS; ZNO NANOPARTICLES; CYCLE PROGRESSION; CELLULAR TOXICITY; GENE-EXPRESSION; CANCER CELLS; CYTOTOXICITY;
D O I
10.3390/ijms18122702
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nanotechnology is an emerging discipline that studies matters at the nanoscale level. Eventually, the goal is to manipulate matters at the atomic level to serve mankind. One growing area in nanotechnology is biomedical applications, which involve disease management and the discovery of basic biological principles. In this review, we discuss characteristics of nanomaterials, with an emphasis on transition metal oxide nanoparticles that influence cytotoxicity. Identification of those properties may lead to the design of more efficient and safer nanosized products for various industrial purposes and provide guidance for assessment of human and environmental health risk. We then investigate biochemical and molecular mechanisms of cytotoxicity that include oxidative stress-induced cellular events and alteration of the pathways pertaining to intracellular calcium homeostasis. All the stresses lead to cell injuries and death. Furthermore, as exposure to nanoparticles results in deregulation of the cell cycle (i.e., interfering with cell proliferation), the change in cell number is a function of cell killing and the suppression of cell proliferation. Collectively, the review article provides insights into the complexity of nanotoxicology.
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页数:13
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