内吞作用
转铁蛋白
细胞内
内吞循环
内化
内体
α-vβ-3
细胞生物学
整合素
共焦显微镜
亚历山福禄
化学
转铁蛋白受体
共焦
药物输送
体外
纳米医学
药理学
医学
生物
生物化学
纳米技术
材料科学
纳米颗粒
荧光
细胞
量子力学
维生素连接蛋白
物理
有机化学
数学
几何学
作者
Yanan Cui,Suxin Li,Binlong Chen,Bing He,Lan Yuan,Wenbing Dai,Hua Zhang,Xueqing Wang,Qiang Zhang
出处
期刊:Current Pharmaceutical Biotechnology
[Bentham Science]
日期:2017-11-10
卷期号:18 (8)
被引量:2
标识
DOI:10.2174/1389201018666171004150050
摘要
Among the many researches on cellular uptake and intracellular trafficking pathways of αvβ3-targeted nanomedicines, a large number of studies utilize serum-free medium to evaluate drug effects and cellular mechanisms in vitro whether the medium is serum free or not has not been paid much attention.The aim of this study was to assess the impact of serum on αvβ3-mediated endocytosis and intracellular trafficking pathways. cRGDfK conjugated with Alexa Fluor® 555 was used to recognize αvβ3 integrins specifically. Transferrin-Alexa Fluor® 488 conjugates were selected as the intracellular trafficking pathway markers by real-time confocal analysis method using confocal laser-scanning microscope.The results showed that after internalization, cRGDfK showed perfect colocalization with transferrin (Tfn) when the cells were cultured in serum-free medium, but manifested obvious separation from Tfn to recycle back to the plasma membrane when the cells were cultured in complete medium. cRGDfK travels two quite different pathways under different culture conditions.We strongly recommended that when the intracellular mechanisms or pharmacodynamics of α vβ 3-targeted nanomedicines was investigated, serum free medium or medium with serum should be taken into consideration. We hope this paper will provide helpful suggestions for studies on α v β 3- targeted drug delivery system.
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