A single-cell analysis platform for electrochemiluminescent detection of platelets adhesion to endothelial cells based on Au@DL-ZnCQDs nanoprobes

被引:17
作者
Long, Dongping [1 ]
Shang, Yunfei [2 ]
Qiu, Youyi [1 ]
Zhou, Bin [1 ]
Yang, Peihui [1 ]
机构
[1] Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China
[2] Beijing Inst Technol, Dept Environm Engn, Zhuhai Campus, Zhuhai 519088, Peoples R China
基金
中国国家自然科学基金;
关键词
Single-cell analysis; Au@DL-ZnCQDs nanoprobes; Platelets adhesion to endothelial cells; E-selectin; ON PHOTOELECTROCHEMICAL IMMUNOASSAY; IN-VITRO; DYNAMIC EVALUATION; PLASMA-MEMBRANE; CARBON DOTS; LABEL-FREE; MECHANISMS; NANOPARTICLES; AMPLIFICATION; IMMUNOSENSOR;
D O I
10.1016/j.bios.2017.11.058
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel single-cell analysis platform (SCA) was developed for the investigation of platelets adhesion to single human umbilical vein endothelial cell (HUVEC) via using the adhesion molecule (E-selectin) on the damaged HUVEC as the marker site, and integrating electrochemiluminescence (ECL) with the ultrasensitive Au@DL-ZnCQDs nanoprobes. The Au@DL-ZnCQDs nanocomposite, a kind of double layer zinc-coadsorbed carbon quantum dot (ZnCQDs) core-shell nanoprobe, was firstly constructed by using gold nanoparticles (AuNPs) as the core to load with ZnCQDs and then the citrate-modified silver nanoparticles (AgNPs) as the bridge to link AuNPs-ZnCQDs with ZnCQDs to form the core-shell with double layer ZnCQDs (DL-ZnCQDs) nanoprobe, revealed a 10 fold signal amplification. The H2O2-induced oxidative damage HUVECs were utilized as the cellular model on which anti-E-selectin functionalized nanoprobes specially recognized E-selectin, the SCA showed that the ECL signals decreased with platelets adhesion to single HUVEC. The proposed SCA could effectively and dynamically monitor the adhesion between single HUVEC and platelets in the absence and presence of collagen activation, moreover, be able to quantitatively detect the number of platelets adhesion to single HUVEC, and show a good analytical performance with linear range from 1 to 15 platelets. In contrast, the HUVEC was down-regulated the expression of adhesion molecules by treating with quercetin inhibitor, and the SCA also exhibited the feasibility for analysis of platelets adhesion to single HUVEC. Therefore, the single-cell analysis platform provided a novel and promising protocol for analysis of the single intercellular adhesion, and it will be beneficial to elucidate the pathogenesis of cardiovascular diseases.
引用
收藏
页码:553 / 559
页数:7
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