Department of Electrical and Computer Engineering, Michigan State University, East Lansing, MI 48824, USA.
Nanoscale. 2018 Jul 9;10(26):12704-12712. doi: 10.1039/c8nr02600a.
Delivering molecules onto the plasma membrane of single cells is still a challenging task in profiling cell signaling pathways with single cell resolution. We demonstrated that a large quantity of molecules could be targeted and released onto the membrane of individual cells to trigger signaling responses. This is achieved by a porous pen nanodeposition (PPN) method, in which a multilayer porous structure, serving as a reservoir for a large amount of molecules, is formed on an atomic force microscope (AFM) tip using layer-by-layer assembly and post processing. To demonstrate its capability for single cell membrane drug delivery, PPN was employed to induce a calcium flux triggered by the binding of released antibodies to membrane antigens in an autoimmune skin disease model. This calcium signal propagates from the target cell to its neighbors in a matter of seconds, proving the theory of intercellular communication through cell-cell junctions. Collectively, these results demonstrated the effectiveness of PPN in membrane drug delivery for single cells; to the best of our knowledge, this is the first technique that can perform the targeted transport and delivery in single cell resolution, paving the way for probing complex signaling interactions in multicellular settings.
将分子递送到单细胞的质膜仍然是在单细胞分辨率下分析细胞信号通路的一项具有挑战性的任务。我们证明了可以将大量分子靶向并释放到单个细胞的膜上,以触发信号反应。这是通过多孔笔纳米沉积(PPN)方法实现的,其中使用层层组装和后处理在原子力显微镜(AFM)尖端上形成多层多孔结构,作为大量分子的储库。为了证明其用于单细胞膜药物递送的能力,使用 PPN 诱导由释放的抗体与自身免疫性皮肤病模型中的膜抗原结合引发的钙通量。该钙信号在数秒内从靶细胞传播到其邻近细胞,证明了通过细胞-细胞连接进行细胞间通讯的理论。总之,这些结果证明了 PPN 在单细胞膜药物递送中的有效性;据我们所知,这是第一种能够以单细胞分辨率进行靶向运输和递送的技术,为在多细胞环境中探测复杂的信号相互作用铺平了道路。