Shubhrasmita Sahu Subhashree, Sarkar Parijat, Chattopadhyay Amitabha
CSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad 500 007, India; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201 002, India.
CSIR-Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad 500 007, India; Department of Biochemistry, Stanford University, School of Medicine, Stanford, CA 94305, USA.
Methods. 2024 Oct;230:44-58. doi: 10.1016/j.ymeth.2024.07.009. Epub 2024 Jul 27.
The actin cytoskeleton is involved in a large number of cellular signaling events in addition to providing structural integrity to the cell. Actin polymerization is a key event during cellular signaling. Although the role of actin cytoskeleton in cellular processes such as trafficking and motility has been extensively studied, the reorganization of the actin cytoskeleton upon signaling has been rarely explored due to lack of suitable assays. Keeping in mind this lacuna, we developed a confocal microscopy based approach that relies on high magnification imaging of cellular F-actin, followed by image reconstruction using commercially available software. In this review, we discuss the context and relevance of actin quantitation, followed by a detailed hands-on approach of the methodology involved with specific points on troubleshooting and useful precautions. In the latter part of the review, we elucidate the method by discussing applications of actin quantitation from our work in several important problems in contemporary membrane biology ranging from pathogen entry into host cells, to GPCR signaling and membrane-cytoskeleton interaction. We envision that future discovery of cell-permeable novel fluorescent probes, in combination with genetically encoded actin-binding reporters, would allow real-time visualization of actin cytoskeleton dynamics to gain deeper insights into active cellular processes in health and disease.
肌动蛋白细胞骨架除了为细胞提供结构完整性外,还参与大量细胞信号转导事件。肌动蛋白聚合是细胞信号转导过程中的关键事件。尽管肌动蛋白细胞骨架在诸如运输和运动等细胞过程中的作用已得到广泛研究,但由于缺乏合适的检测方法,信号转导时肌动蛋白细胞骨架的重组很少被探索。考虑到这一空白,我们开发了一种基于共聚焦显微镜的方法,该方法依赖于对细胞F-肌动蛋白的高倍成像,然后使用商业软件进行图像重建。在本综述中,我们讨论了肌动蛋白定量的背景和相关性,随后详细介绍了该方法的实际操作步骤,包括故障排除的具体要点和有用的注意事项。在综述的后半部分,我们通过讨论肌动蛋白定量在当代膜生物学的几个重要问题中的应用来阐明该方法,这些问题包括病原体进入宿主细胞、G蛋白偶联受体信号转导以及膜-细胞骨架相互作用等。我们设想,未来结合可渗透细胞新型荧光探针与基因编码的肌动蛋白结合报告基因,将能够实时可视化肌动蛋白细胞骨架动力学,从而更深入地了解健康和疾病状态下的活跃细胞过程。