Kawanishi Toru, Heilig Ann Kathrin, Shimada Atsuko, Takeda Hiroyuki
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Tokyo, Japan.
Bio Protoc. 2023 Jul 5;13(13):e4710. doi: 10.21769/BioProtoc.4710.
ellular protrusions are fundamental structures for a wide variety of cellular behaviors, such as cell migration, cell-cell interaction, and signal reception. Visualization of cellular protrusions in living cells can be achieved by labeling of cytoskeletal actin with genetically encoded fluorescent probes. Here, we describe a detailed experimental procedure to visualize cellular protrusions in medaka embryos, which consists of the following steps: preparation of Actin-Chromobody-GFP and α-bungarotoxin mRNAs for actin labeling and immobilization of the embryo, respectively; microinjection of the mRNAs into embryos in a mosaic fashion to sparsely label individual cells; removal of the hard chorion, which hampers observation; and visualization of cellular protrusions in the embryo with a confocal microscope. Overall, our protocol provides a simple method to reveal cellular protrusions in vivo by confocal microscopy.
细胞突起是多种细胞行为的基本结构,如细胞迁移、细胞间相互作用和信号接收。通过用基因编码的荧光探针标记细胞骨架肌动蛋白,可以实现活细胞中细胞突起的可视化。在这里,我们描述了一个详细的实验程序,用于在青鳉胚胎中可视化细胞突起,该程序包括以下步骤:分别制备用于肌动蛋白标记的肌动蛋白-染色体体-GFP和用于胚胎固定的α-银环蛇毒素mRNA;以镶嵌方式将mRNA显微注射到胚胎中,以稀疏标记单个细胞;去除妨碍观察的硬绒毛膜;并用共聚焦显微镜观察胚胎中的细胞突起。总的来说,我们的方案提供了一种通过共聚焦显微镜在体内揭示细胞突起的简单方法。