Simcox Amanda
Department of Molecular Genetics, Ohio State University, Columbus, OH, USA.
Methods Mol Biol. 2013;945:1-11. doi: 10.1007/978-1-62703-125-7_1.
Drosophila epithelial research is at the forefront of the field; however, there are no well-characterized epithelial cell lines that could provide a complementary in vitro model for studies conducted in vivo. Here, a protocol is described that produces epithelial cell lines. The method uses genetic manipulation of oncogenes or tumor suppressors to induce embryonic primary culture cells to rapidly progress to permanent cell lines. It is, however, a general method and the type of cells that comprise a given line is not controlled experimentally. Indeed, only a small fraction of the lines produced are epithelial in character. For this reason, additional work needs to be done to develop a more robust epithelial cell-specific protocol. It is expected that Drosophila epithelial cell lines will have great utility for in vitro analysis of epithelial biology, particularly high-throughput analyses such as RNAi screens.
果蝇上皮细胞研究处于该领域的前沿;然而,目前尚无特征明确的上皮细胞系能够为体内研究提供互补的体外模型。本文描述了一种产生上皮细胞系的方法。该方法利用癌基因或肿瘤抑制基因的基因操作,诱导胚胎原代培养细胞快速发展为永久细胞系。然而,这是一种通用方法,组成特定细胞系的细胞类型无法通过实验控制。实际上,所产生的细胞系中只有一小部分具有上皮细胞特征。因此,需要开展更多工作来开发一种更可靠的上皮细胞特异性方法。预计果蝇上皮细胞系将在体外上皮生物学分析中具有很大用途,尤其是在诸如RNA干扰筛选等高通量分析中。