Size-Dependent Cell Uptake of Protein-Coated Graphene Oxide Nanosheets

被引:316
作者
Mu, Qingxin [1 ]
Su, Gaoxing [1 ,2 ]
Li, Liwen [1 ,2 ]
Gilbertson, Ben O. [3 ]
Yu, Lam H. [3 ]
Zhang, Qiu [2 ]
Sun, Ya-Ping [4 ,5 ]
Yan, Bing [1 ,2 ]
机构
[1] St Jude Childrens Res Hosp, Dept Chem Biol & Therapeut, Memphis, TN 38105 USA
[2] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
[3] Univ Memphis, Dept Phys, Memphis, TN 38152 USA
[4] Clemson Univ, Dept Chem, Clemson, SC 29634 USA
[5] Clemson Univ, Lab Emerging Mat & Technol, Clemson, SC 29634 USA
基金
中国国家自然科学基金;
关键词
graphene oxide nanosheets; protein binding; cell uptake; clathrin-mediated endocytosis; phagocytosis; size dependence; FUNCTIONALIZED CARBON NANOTUBES; PHOTOTHERMAL THERAPY; GOLD NANOPARTICLES; STEM-CELLS; CYTOTOXICITY; PHAGOCYTOSIS;
D O I
10.1021/am300253c
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
As an emerging applied material, graphene has shown tremendous application potential in many fields, including biomedicine. However, the biological behavior of these nanosheets, especially their interactions with cells, is not well understood. Here, we report our findings about the cell surface adhesion, subcellular locations, and size-dependent uptake mechanisms of protein-coated graphene oxide nanosheets (PCGO). Small nanosheets enter cells mainly through clathrin-mediated endocytosis, and the increase of graphene size enhances phagocytotic uptake of the nanosheets. These findings will facilitate biomedical and toxicologic studies of graphenes and provide fundamental understanding of interactions at the interface of two-dimensional nanostructures and biological systems.
引用
收藏
页码:2259 / 2266
页数:8
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