Cambi Alessandra, Lidke Diane S, Arndt-Jovin Donna J, Figdor Carl G, Jovin Thomas M
Department of Molecular Biology, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Nano Lett. 2007 Apr;7(4):970-7. doi: 10.1021/nl0700503. Epub 2007 Mar 28.
The dendritic cell (DC) specific pathogen-uptake receptor (DC-SIGN) internalizes antigens for degradation and presentation onto MHC molecules. At the cell membrane, DC-SIGN forms nanoclusters that facilitate virus capture. However, internalized viruses, such as HIV-1, escape degradation. Here, we exploit ligand-conjugated, virus-sized, highly photostable quantum dots (QDs) to monitor in living cells antigen binding, entry, and trafficking. The antigen-coated QDs specific uptake and persistence in live DCs open the possibility for tracking antigen-presenting cells in vivo.
树突状细胞(DC)特异性病原体摄取受体(DC-SIGN)将抗原内化以进行降解并呈递到MHC分子上。在细胞膜上,DC-SIGN形成纳米簇以促进病毒捕获。然而,内化的病毒,如HIV-1,逃避降解。在这里,我们利用配体偶联的、病毒大小的、高光稳定性量子点(QD)来监测活细胞中的抗原结合、进入和运输。抗原包被的量子点在活的树突状细胞中的特异性摄取和持久性为在体内追踪抗原呈递细胞提供了可能性。