Karlsruhe Institute of Technology (KIT), Institute for Biological Interfaces (IBG 1), Hermann-von-Helmholtz-Platz 1, 76344, Eggenstein-Leopoldshafen, Germany.
Leibniz Research Center for Working Environment and Human Factors (IfADo) at TU Dortmund, Ardeystrasse 67, 44139, Dortmund, Germany.
Chembiochem. 2016 Mar 15;17(6):486-92. doi: 10.1002/cbic.201500629. Epub 2016 Feb 17.
Natural killer (NK) cells are at the junction of the innate and the adaptive immune response and play a very important role in host defense against viral infections and cancer. They have numerous cell surface receptors that activate or inhibit various intracellular signaling cascades that are then integrated to determine the functional activity of these cells. Here we present a surface-based approach that aims to tackle the largely unknown molecular mechanisms of signal integration. We use DNA microarrays containing capture oligonucleotides for the DNA-directed immobilization (DDI) of oligonucleotide-tagged αCD16 antibodies as ligands for NK cells. We demonstrate that the resulting surfaces can be gradually tuned in terms of ligand density to trigger the activation of living NK cells, as evidenced by degranulation, the release of cytokines, and intracellular Ca(2+) flux, measured at the level of single cells.
自然杀伤 (NK) 细胞位于先天免疫和适应性免疫反应的交界处,在宿主防御病毒感染和癌症方面发挥着非常重要的作用。它们具有许多细胞表面受体,这些受体可以激活或抑制各种细胞内信号级联反应,然后将这些反应整合起来以确定这些细胞的功能活性。在这里,我们提出了一种基于表面的方法,旨在解决信号整合的分子机制很大程度上未知的问题。我们使用包含捕获寡核苷酸的 DNA 微阵列,用于寡核苷酸标记的 αCD16 抗体的 DNA 定向固定(DDI)作为 NK 细胞的配体。我们证明,通过逐渐调整配体密度,可以实现表面的调控,从而触发活 NK 细胞的激活,这可以通过脱颗粒、细胞因子的释放和细胞内 Ca(2+) 流来证明,这些都是在单细胞水平上测量的。