CIMUS (Department of Physiology), School of Medicine, University of Santiago de Compostela, Avd. Barcelona, 15782, Santiago de Compostela, Spain,
Cytotechnology. 2013 Aug;65(4):523-32. doi: 10.1007/s10616-012-9509-3. Epub 2012 Nov 7.
The mouse retina constitutes an important research model for studies aiming to unravel the cellular and molecular mechanisms underlying ocular diseases. The accessibility of this tissue and its feasibility to directly obtain neurons from it has increased the number of studies culturing mouse retina, mainly retinal cell suspensions. However, to address many questions concerning retinal diseases and protein function, the organotypic structure must be maintained, so it becomes important to devise methods to transfect and culture whole retinas without disturbing their cellular structure. Moreover, the postmitotic stage of retinal neurons makes them reluctant to commonly used transfection techniques. For this purpose some published methods employ in vivo virus-based transfection techniques or biolistics, methods that present some constraints. Here we report for the first time a method to transfect P15-P20 whole murine retinas via nucleofection, where nucleic acids are directly delivered to the cell nuclei, allowing in vitro transfection of postmitotic cells. A detailed protocol for successful retina extraction, organotypic culture, nucleofection, histological procedures and imaging is described. In our hands the A-33 nucleofector program shows the highest transfection efficiency. Whole flat-mount retinas and cryosections from transfected retinas were imaged by epifluorescence and confocal microscopy, showing that not only cells located in the outermost retinal layers, but also those in inner retinal layers are transfected. In conclusion, we present a novel method to successfully transfect postnatal whole murine retina via nucleofection, showing that retina can be successfully nucleofected after some optimization steps.
小鼠视网膜是研究眼部疾病细胞和分子机制的重要模型。由于该组织易于获取,并且可以直接从其获得神经元,因此培养小鼠视网膜的研究,主要是视网膜细胞悬浮液的研究越来越多。但是,为了解决许多与视网膜疾病和蛋白质功能有关的问题,必须保持器官样结构,因此设计方法以不干扰其细胞结构的方式转染和培养整个视网膜变得很重要。此外,视网膜神经元的有丝分裂后阶段使其难以使用常用的转染技术。为此,一些已发表的方法采用了体内基于病毒的转染技术或生物弹道学,这些方法存在一些局限性。在这里,我们首次报道了一种通过电穿孔转染 P15-P20 整个鼠视网膜的方法,其中核酸直接递送至细胞核,从而可以对有丝分裂后细胞进行体外转染。详细描述了成功提取视网膜,器官样培养,电穿孔,组织学程序和成像的方案。在我们的实验中,A-33 电穿孔程序显示出最高的转染效率。通过荧光显微镜和共聚焦显微镜对转染的整个平展视网膜和冷冻切片进行成像,结果表明,不仅是最外层视网膜层中的细胞,而且是内层视网膜层中的细胞都被转染了。总之,我们提出了一种通过电穿孔成功转染新生后整个小鼠视网膜的新方法,表明经过一些优化步骤后,视网膜可以成功进行电穿孔。