University of St. Andrews, School of Physics and Astronomy, North Haugh, St. Andrews, Fife, Scotland, United Kingdom.
J Biomed Opt. 2010 Jul-Aug;15(4):041507. doi: 10.1117/1.3430733.
Recently, femtosecond laser pulses have been utilized for the targeted introduction of genetic matter into mammalian cells. This rapidly expanding and developing novel optical technique using a tightly focused laser light beam is called phototransfection. Extending previous studies [Stevenson et al., Opt. Express 14, 7125-7133 (2006)], we show that femtosecond lasers can be used to phototransfect a range of different cell lines, and specifically that this novel technology can also transfect mouse embryonic stem cell colonies with approximately 25% efficiency. Notably, we show the ability of differentiating these cells into the extraembryonic endoderm using phototransfection. Furthermore, we present two new findings aimed at optimizing the phototransfection method and improving applicability: first, the influence of the cell passage number on the transfection efficiency is explored and, second, the ability to enhance the transfection efficiency via whole culture treatments. Our results should encourage wider uptake of this methodology.
最近,飞秒激光脉冲已被用于将遗传物质靶向引入哺乳动物细胞。这种利用聚焦激光束的快速扩展和发展的新型光学技术称为光转染。在前人的研究基础上[Stevenson 等人,Opt. Express 14, 7125-7133(2006)],我们表明飞秒激光可用于转染多种不同的细胞系,特别是该新技术还可以将大约 25%的效率转染入小鼠胚胎干细胞集落。值得注意的是,我们展示了使用光转染将这些细胞分化为胚胎外内胚层的能力。此外,我们提出了两项旨在优化光转染方法和提高适用性的新发现:首先,探索了细胞传代数对转染效率的影响,其次,通过整个培养物处理提高转染效率的能力。我们的结果应鼓励更广泛地采用这种方法。