Endocytosis Pathways of Endothelial Cell Derived Exosomes

被引:43
作者
Banizs, Anna B. [1 ]
Huang, Tao [1 ]
Nakamoto, Robert K. [2 ]
Shi, Weibin [1 ]
He, Jiang [1 ]
机构
[1] Univ Virginia, Dept Radiol & Med Imaging, POB 801339,480 Ray C Hunt Dr,282, Charlottesville, VA 22903 USA
[2] Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22903 USA
基金
美国国家卫生研究院;
关键词
exosome; extracellular vesicles; endothelial cells; endocytosis; nanomedicine; MECHANISMS; INTERNALIZATION; MODEL;
D O I
10.1021/acs.molpharmaceut.8b00765
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Nanosized extracellular vesicles (EVs) possess the natural machinery needed to enter selectively and transmit complex molecular messages efficiently into targeted cells. The intracellular fate of the vesicular cargos depends on the route of internalization. Therefore, understanding the mechanism of attachment and subsequent intake of these vesicles (before and after exerting any modification) is imperative. Here the extent of communication, the uptake kinetics, and the pathways of endothelial EVs into endothelial cells in the presence of specific pharmacological inhibitors were assessed by imaging flow cytometry. The results showed that the uptake of endothelial EVs into endothelial cells was largely an energy-dependent process using predominantly a receptor-mediated, clathrin-dependent pathway.
引用
收藏
页码:5585 / 5590
页数:6
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