Centre for Neuroscience, Flinders Medical Science and Technology, School of Medicine, Flinders University, Adelaide, SA, Australia.
Neurochem Res. 2010 Nov;35(11):1771-9. doi: 10.1007/s11064-010-0243-y. Epub 2010 Aug 21.
Nucleofection is a powerful non-viral transfection technique that can deliver plasmid DNA with high efficiency to cells that are traditionally difficult to transfect. In this study, we demonstrate that nucleofection of astrocytes grown in primary cell culture resulted in 76 ± 9% transfected cells and low cytotoxicity. However, the nucleofected astrocytes showed a reduced re-attachment to the growth media when replated and subsequent impairment of proliferation. This led to substantially decreased cell densities during the initial 72 h following transfection. Furthermore, these cells were less efficient at producing wound closure in a scratch model of injury. Nucleofection also resulted in the generation of a small proportion of polynucleated cells. The findings demonstrate that nucleofection provides a valuable technique for delivering DNA to astrocytes in culture. However, considerable care is needed in designing and interpreting such studies because of long-lasting changes induced in key properties of these cells by the nucleofection process.
转染是一种强大的非病毒转染技术,可以将质粒 DNA 高效地递送到传统上难以转染的细胞中。在这项研究中,我们证明了在原代细胞培养中对星形胶质细胞进行转染,可获得 76 ± 9%的转染细胞,且细胞毒性低。然而,当重新接种到生长培养基中时,转染的星形胶质细胞的再附着能力降低,随后增殖受损。这导致转染后最初 72 小时内细胞密度显著降低。此外,这些细胞在划痕损伤模型中闭合伤口的效率较低。转染还导致一小部分多核细胞的产生。这些发现表明,转染为在培养的星形胶质细胞中递送 DNA 提供了一种有价值的技术。然而,由于核转染过程对这些细胞的关键特性产生了持久的变化,因此在设计和解释此类研究时需要非常小心。