van Grinsven Erinke, Prunier Chloé, Vrisekoop Nienke, Ritsma Laila
Department of Respiratory Medicine, Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
Department of Molecular Cell Biology, Leiden University Medical Center, Einthovenweg 20, 2333 ZC, Leiden, The Netherlands.
Methods Mol Biol. 2017;1563:51-71. doi: 10.1007/978-1-4939-6810-7_4.
Two-photon intravital microscopy (2P-IVM) is an advanced imaging platform that allows the visualization of dynamic processes at subcellular resolution in vivo. Dynamic processes like cell migration, cell proliferation, cell-cell interactions, and cell signaling have an interactive character and occur in complex environments. Hence, it is of pivotal importance to study these processes in living animals, using for example 2P-IVM. 2P-IVM can be performed on a variety of tissues, from the skin of the animal to internal organs, and a variety of methods can be utilized to perform 2P-IVM on these tissues. Here, we discuss the protocols and considerations for four of those 2P-IVM methods, namely tissue explant imaging, skin imaging, surgical exposure imaging, and multi-day window imaging. We carefully compare and explain in depth how to set up each method. Lastly, in the notes section we mention some alternative solutions for the 2P-IVM methods described. In conclusion, this protocol can be used as a guide towards deciding which 2P-IVM method to use and to enable the setup of this method.
双光子活体显微镜成像(2P-IVM)是一种先进的成像平台,可在体内以亚细胞分辨率可视化动态过程。细胞迁移、细胞增殖、细胞间相互作用和细胞信号传导等动态过程具有交互特性,且发生在复杂环境中。因此,使用例如2P-IVM在活体动物中研究这些过程至关重要。2P-IVM可在从动物皮肤到内部器官的各种组织上进行,并且可以利用多种方法在这些组织上进行2P-IVM。在此,我们讨论其中四种2P-IVM方法的方案和注意事项,即组织外植体成像、皮肤成像、手术暴露成像和多日窗口成像。我们仔细比较并深入解释如何设置每种方法。最后,在注释部分我们提及了所描述的2P-IVM方法的一些替代解决方案。总之,本方案可作为决定使用哪种2P-IVM方法以及进行该方法设置的指南。