Nanoparticle interactions with live cells: Quantitative fluorescence microscopy of nanoparticle size effects

Beilstein Journal of Nanotechnology

G. Ulrich Nienhaus¹  Li Shang¹  Linxiao Yang¹  Karin Nienhaus¹  Thomas Simmet²  Volker Mailänder³  Katharina Landfester³  Xiue Jiang⁴ 

[1] Institute of Applied Physics, Karlsruhe Institute of Technology (KIT), 76131 Karlsruhe, Germany;Institute of Pharmacology of Natural Products & Clinical Pharmacology, Ulm University, D-89081 Ulm, Germany;Max Planck Institute for Polymer Research, 55128 Mainz, Germany;State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Science, Changchun, 130022, China;

关键词: cell membrane;    endocytosis;    fluorescence microscopy;    nanoparticle;    size effect;   

DOI  :  10.3762/bjnano.5.248

来源: DOAJ

【 摘 要 】

Engineered nanomaterials are known to enter human cells, often via active endocytosis. Mechanistic details of the interactions between nanoparticles (NPs) with cells are still not well enough understood. NP size is a key parameter that controls the endocytic mechanism and affects the cellular uptake yield. Therefore, we have systematically analyzed the cellular uptake of fluorescent NPs in the size range of 3.3–100 nm (diameter) by live cells. By using spinning disk confocal microscopy in combination with quantitative image analysis, we studied the time courses of NP association with the cell membrane and subsequent internalization. NPs with diameters of less than 10 nm were observed to accumulate at the plasma membrane before being internalized by the cells. In contrast, larger NPs (100 nm) were directly internalized without prior accumulation at the plasma membrane, regardless of their surface charges. We attribute this distinct size dependence to the requirement of a sufficiently strong local interaction of the NPs with the endocytic machinery in order to trigger the subsequent internalization.

【 授权许可】

Unknown