The cytotoxicities in prokaryote and eukaryote varied for CdSe and CdSe/ZnS quantum dots and differed from cadmium ions

被引:25
作者
Hu, Liang [1 ]
Zhong, Hui [2 ]
He, Zhiguo [1 ]
机构
[1] Cent S Univ, Sch Minerals Proc & Bioengn, Key Lab Biohydromet, Minist Educ, Changsha 410083, Hunan, Peoples R China
[2] Cent S Univ, Sch Life Sci, Changsha 410012, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Quantum dots; Prokaryote; Eukaryote; Cadmium ions; Cellular uptake; Particle-specific toxicity; STABILIZED NANO-CHLORAPATITE; H+-ATPASE ACTIVITY; PHANEROCHAETE-CHRYSOSPORIUM; PLASMA-MEMBRANE; CELLULAR UPTAKE; OXIDE NANOPARTICLES; PB IMMOBILIZATION; LANDFILL LEACHATE; OXIDATIVE STRESS; TOXICITY;
D O I
10.1016/j.ecoenv.2019.06.027
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The present study focused on the bioaccumulation and cytotoxicities of Cd2+, CdSe quantum dots (QDs) and CdSe/ZnS QDs in Escherichia coli (E. coli, represents prokaryotic system) and Phanerochaete chrysosporium (P. chrysosporium, represents eukaryotic system), respectively. Two types of QDs were characterized by transmission electron microscopy (TEM) and dynamic light scattering. The inductively coupled plasma optical emission spectrometer results showed that the bioaccumulation amounts of CdSe QDs by E. coli and P. chrysosporium were larger than those of CdSe/ZnS QDs due to the smaller particle size and less negative surface charges of CdSe QDs. Confocal microscopy and TEM results showed that there was an interaction between QDs and cells, and QDs have entered into the cells eventually, leading to the change of cell morphology. Plasma membrane fluidities and membrane H+-ATPase activities of E. coli and P. chrysosporium decreased gradually with the increasing concentrations of Cd2+, CdSe and CdSe/ZnS QDs. Results of the cell viabilities and intracellular reactive oxygen species levels indicated that the induced cytotoxicities were decreased as follows: CdSe QDs > CdSe/ZnS QDs > Cd2+. These findings suggested that the cytotoxicity of QDs was not only attributed to their heavy metal components, but also related to their nanosize effects which could induce particle-specific toxicity. The above results offer valuable information for exploring the cytotoxicity mechanism of QDs in prokaryote and eukaryote.
引用
收藏
页码:336 / 344
页数:9
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