Endo- and Exocytosis of Zwitterionic Quantum Dot Nanoparticles by Live HeLa Cells

被引:261
作者
Jiang, Xiue [1 ,2 ,3 ]
Rocker, Carlheinz [3 ]
Hafner, Margit [3 ]
Brandholt, Stefan [1 ,2 ]
Dorlich, Rene M. [1 ,2 ]
Nienhaus, G. Ulrich [1 ,2 ,4 ]
机构
[1] KIT, Inst Appl Phys, D-76131 Karlsruhe, Germany
[2] KIT, CFN, D-76131 Karlsruhe, Germany
[3] Univ Ulm, Inst Biophys, D-89081 Ulm, Germany
[4] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
关键词
quantum dots; endoytosls; exocytosis; live cell imaging; uptake mechanism; uptake inhibition; confocal microscopy; CLATHRIN-MEDIATED ENDOCYTOSIS; LIVING CELLS; CELLULAR UPTAKE; PROTEIN CORONA; SIZE; INTERNALIZATION; FLUORESCENCE; INHIBITION; PARTICLES; MECHANISM;
D O I
10.1021/nn101277w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Uptake and intracellular transport of D-penicillamine coated quantum dots (DPA QDs) of 4 nm radius by live HeLa cells have been investigated systematically by spinning disk and 4Pi confocal microscopies Unlike larger nanoparticles, these small DPA Qds were observed to accumulate at the plasma membrane prior to internalization, and the uptake efficiency scaled nonlinearly with the nanoparticle concentration Both observations indicate that a critical threshold density has to be exceeded for triggering the internalization process By using specific inhibitors we showed that DPA QDs were predominantly internalized by clathnn mediated endocytosis and to smaller extent by macropinocytosis Clusters of DPA QDs were found in endosomes, which were actively transported along microtubules toward the pennuclear region Later on, a significant fraction of endocytosed DPA-QDs were found in lysosomes, while others were actively transported to the cell penphery and exocytosed with a half life of 21 min
引用
收藏
页码:6787 / 6797
页数:11
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