Xiao Xiangwei, Guo Ping, Prasadan Krishna, Shiota Chiyo, Peirish Lauren, Fischbach Shane, Song Zewen, Gaffar Iljana, Wiersch John, El-Gohary Yousef, Husain Sohail Z, Gittes George K
Division of Pediatric Surgery, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Division of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Nat Protoc. 2014 Dec;9(12):2719-24. doi: 10.1038/nprot.2014.183. Epub 2014 Oct 30.
Genetic manipulations, with or without lineage tracing for specific pancreatic cell types, are very powerful tools for studying diabetes, pancreatitis and pancreatic cancer. Nevertheless, the use of Cre/loxP systems to conditionally activate or inactivate the expression of genes in a cell type- and/or temporal-specific manner is not applicable to cell tracing and/or gene manipulations in more than one lineage at a time. Here we report a technique that allows efficient delivery of dyes for cell tagging into the mouse pancreas through the duct system, and that also delivers viruses carrying transgenes or siRNA under a specific promoter. When this technique is applied in genetically modified mice, it enables the investigator to perform either double lineage tracing or cell lineage tracing combined with gene manipulation in a second lineage. The technique requires <40 min.
基因操作,无论有无对特定胰腺细胞类型进行谱系追踪,都是研究糖尿病、胰腺炎和胰腺癌的非常强大的工具。然而,使用Cre/loxP系统以细胞类型和/或时间特异性方式有条件地激活或失活基因表达,并不适用于同时对多个谱系进行细胞追踪和/或基因操作。在此,我们报告一种技术,该技术允许通过导管系统将用于细胞标记的染料高效递送至小鼠胰腺,并且还能在特定启动子下递送携带转基因或小干扰RNA(siRNA)的病毒。当将该技术应用于基因修饰小鼠时,它使研究人员能够在第二个谱系中进行双谱系追踪或细胞谱系追踪并结合基因操作。该技术所需时间不到40分钟。