Heffernan Corey, Maurel Patrice
Department of Biological Sciences, Rutgers University, Newark, NJ, USA.
Methods Mol Biol. 2018;1739:177-193. doi: 10.1007/978-1-4939-7649-2_12.
Lentiviral transduction is a gene delivery method that provides numerous advantages over direct transfection and traditional retroviral or adenoviral delivery methods. It facilitates for the transduction of primary cells inherently difficult to transfect, delivers constructs of interest to nondividing as well as dividing cells, and permits the long-term expression of sizable DNA inserts (e.g., <7 kb). The study of peripheral nerve myelination at the molecular level has long benefited from the Schwann cells/dorsal root ganglia (DRG) neurons myelinating co-culture system. As this culture system takes about a month to develop and perform experiments with, lentiviral-delivered constructs can be used to manipulate gene expression in Schwann cells and DRG neurons, primary cells that are otherwise resilient to direct transfection. Here we present our protocol for lentiviral production and purification and subsequent infection of large numbers of Schwann cells and/or DRG neurons for the molecular study of peripheral nerve myelination in vitro.
慢病毒转导是一种基因递送方法,与直接转染以及传统的逆转录病毒或腺病毒递送方法相比具有诸多优势。它有助于转导原本难以转染的原代细胞,将感兴趣的构建体递送至非分裂细胞以及分裂细胞,并允许大片段DNA插入物(例如,<7 kb)长期表达。在分子水平上对外周神经髓鞘形成的研究长期以来受益于雪旺细胞/背根神经节(DRG)神经元髓鞘形成共培养系统。由于这种培养系统大约需要一个月的时间来建立并进行实验,慢病毒递送的构建体可用于操纵雪旺细胞和DRG神经元中的基因表达,而这些原代细胞对直接转染具有抗性。在此,我们展示了我们的慢病毒生产、纯化方案,以及随后对大量雪旺细胞和/或DRG神经元进行感染以用于体外外周神经髓鞘形成分子研究的方案。