Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305, USA.
Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Sci Adv. 2018 Oct 31;4(10):eaat8131. doi: 10.1126/sciadv.aat8131. eCollection 2018 Oct.
Intracellular delivery of mRNA, DNA, and other large macromolecules into cells plays an essential role in an array of biological research and clinical therapies. However, current methods yield a wide variation in the amount of material delivered, as well as limitations on the cell types and cargoes possible. Here, we demonstrate quantitatively controlled delivery into a range of primary cells and cell lines with a tight dosage distribution using a nanostraw-electroporation system (NES). In NES, cells are cultured onto track-etched membranes with protruding nanostraws that connect to the fluidic environment beneath the membrane. The tight cell-nanostraw interface focuses applied electric fields to the cell membrane, enabling low-voltage and nondamaging local poration of the cell membrane. Concurrently, the field electrophoretically injects biomolecular cargoes through the nanostraws and into the cell at the same location. We show that the amount of material delivered is precisely controlled by the applied voltage, delivery duration, and reagent concentration. NES is highly effective even for primary cell types or different cell densities, is largely cargo agnostic, and can simultaneously deliver specific ratios of different molecules. Using a simple cell culture well format, the NES delivers into >100,000 cells within 20 s with >95% cell viability, enabling facile, dosage-controlled intracellular delivery for a wide variety of biological applications.
将 mRNA、DNA 和其他大分子物质递送到细胞内,在一系列生物学研究和临床治疗中起着至关重要的作用。然而,目前的方法在递送的物质数量上存在很大差异,并且对可能的细胞类型和货物也有限制。在这里,我们使用纳米线电穿孔系统(NES)展示了对一系列原代细胞和细胞系进行定量控制的递药,具有紧密的剂量分布。在 NES 中,细胞被培养在带有突出纳米线的刻蚀膜上,纳米线与膜下方的流体环境相连。紧密的细胞-纳米线界面将施加的电场聚焦到细胞膜上,从而能够在细胞膜上进行低电压且无损的局部穿孔。同时,电场通过纳米线将生物分子货物电泳注入细胞,并在同一位置注入细胞。我们表明,递送到细胞内的物质数量可以通过施加的电压、递送时间和试剂浓度来精确控制。即使对于原代细胞类型或不同的细胞密度,NES 也非常有效,它在很大程度上不受货物种类的影响,并且可以同时递送到不同分子的特定比例。使用简单的细胞培养小室格式,NES 在 20 秒内可将 >100,000 个细胞的转染效率超过 95%,同时具有高细胞活力,能够实现广泛的生物学应用中的简便、剂量可控的细胞内递送。