Cytotoxicity and Gene Expression in Sarcoma 180 Cells in Response to Spiky Magnetoplasmonic Supraparticles

被引:19
|
作者
Zhou, Hongjian [1 ]
Choi, Sun Il [2 ]
Zou, Fengming [3 ,4 ]
Oh, Sangjin [1 ]
Kim, Ji Eun [2 ]
Hwang, Dae Youn [2 ]
Lee, Jaebeom [1 ]
机构
[1] Pusan Natl Univ, Dept Nano Fus, Dept Nano Fus & Cognomechatron Engn, Pusan 609735, South Korea
[2] Pusan Natl Univ, Dept Biomat Sci, Coll Nat Resources & Life Sci, Miryang 627706, South Korea
[3] Pusan Natl Univ, Dept Nano Fus Technol, Pusan 609735, South Korea
[4] Pusan Natl Univ, Plus Nano Convergence Technol Div BK21, Pusan 609735, South Korea
关键词
concave core-shell nanoparticle; tumor cell; cytotoxicity; microarray; gene expression; GOLD-NANOPARTICLES; NANOCRYSTALS; FABRICATION; FACETS; SHAPE; SIZE;
D O I
10.1021/am504632g
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Multifunctional nanoparticles (NPs) have been designed for a variety of cell imaging and therapeutic applications, and the study of their cellular interactions is crucial to the development of more efficient biomedical applications. Among current nanomaterials, concave core-shell NPs with complex angled geometries are attractive owing to their unique shape-dependent optical and physical properties as well as different tendency for cell interaction. In this study, we investigated the morphology effect of spiky gold-coated iron oxide supraparticles (Fe3O4@Au SPs) on cytotoxicity and global gene expression in sarcoma 180 cells. Cells treated for 7 days with spiky supraparticles (SPs) at concentrations up to 50 mu g/mL showed >90% viability, indicating that these NPs were nontoxic. To shed light on the differences in cytotoxicity, we monitored the expression of 33 315 genes using microarray analysis of SP-treated cells. The 171 up-regulated genes and 181 down-regulated genes in spiky SP-treated cells included Il1b, Spp1, Il18, Rbp4, and Il11ra1, where these genes are mainly involved in cell proliferation, differentiation, and apoptosis. These results suggested that the spiky Fe3O4@Au SPs can induce noncytotoxicity and gene expression in tumor cells, which may be a promising cornerstone on which to base related research such as cyto-/genotoxicology of nanomaterials or the design of nanoscale drug carriers.
引用
收藏
页码:19680 / 19689
页数:10
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