Cellular uptake of fluorophore-labeled glyco-DNA-gold nanoparticles

被引:1
作者
Witten, Katrin G. [1 ]
Ruff, Julie [1 ]
Mohr, Anne [2 ]
Goertz, Dieter [2 ]
Recker, Tobias [2 ]
Rinis, Natalie [2 ]
Rech, Claudia [3 ,4 ]
Elling, Lothar [3 ,4 ]
Mueller-Newen, Gerhard [2 ]
Simon, Ulrich [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Inorgan Chem & JARA Fundamentals Future Info, D-52074 Aachen, Germany
[2] Rhein Westfal TH Aachen, Univ Hosp Aachen, Inst Biochem & Mol Biol, D-52074 Aachen, Germany
[3] Rhein Westfal TH Aachen, Lab Biomat, Inst Biotechnol, D-52074 Aachen, Germany
[4] Rhein Westfal TH Aachen, Helmholtz Inst Biomed Engn, D-52074 Aachen, Germany
关键词
Gold nanoparticles; DNA; Carbohydrates; Cellular uptake; Hepatocytes; ASIALOGLYCOPROTEIN RECEPTOR; SCAVENGER RECEPTORS; LIVER-CELLS; IN-VITRO; DELIVERY; LIGANDS; LECTIN; DETERMINES; PLATFORM; BIOLOGY;
D O I
10.1007/s11051-013-1992-8
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
DNA-functionalized gold nanoparticles (AuNP-DNA) were hybridized with complementary di-N-acetyllactosamine-(di-LacNAc, [3Gal(beta 1-4)GlcNAc(beta 1-]2)-modified oligonucleotides to form glycol-functionalized particles, AuNP-DNA-di-LacNAc. While AuNP-DNA are known to be taken up by cells via scavenger receptors, glycol-functionalized particles have shown to be taken up via asialoglycoprotein receptors (ASGP-R). In this work, the interaction of these new particles with HepG2 cells was analyzed, which express scavenger receptors class B type I (SR-BI) and ASGP-R. To study the contribution of these receptors as potential mediators for cellular uptake, receptor-blocking experiments were performed with d-lactose, a ligand for ASGP-R, Fucoidan, a putative ligand for SR-BI, and a SR-BI blocking antibody. Labeling with Cy5-modified DNA ligands enabled us to monitor the particle uptake by confocal fluorescence microscopy and flow cytometry, in order to discriminate the two putative pathways by competitive binding studies. While SR-BI-antibody and d-lactose had no inhibiting effects on particle uptake Fucoidan led to a complete inhibition. Thus, a receptor-mediated uptake by the two receptors studied could not be proven and therefore other uptake mechanisms have to be considered.
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页数:12
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