Department of Medicine, Division of Nephrology, Indiana University, Indianapolis, IN, USA.
Department of Cellular and Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Dr., Indianapolis, IN 46202, USA.
Methods. 2017 Sep 1;128:95-104. doi: 10.1016/j.ymeth.2017.04.017. Epub 2017 Apr 21.
Intravital microscopy (IVM) is an imaging tool that is capable of detecting subcellular signaling or metabolic events as they occur in tissues in the living animal. Imaging in highly scattering biological tissues, however, is challenging because of the attenuation of signal in images acquired at increasing depths. Depth-dependent signal attenuation is the major impediment to IVM, limiting the depth from which significant data can be obtained. Therefore, making quantitative measurements by IVM requires methods that use internal calibration, or alternatively, a completely different way of evaluating the signals. Here, we describe how ratiometric imaging of genetically encoded biosensor probes can be used to make quantitative measurements of changes in the activity of cell signaling pathways. Then, we describe how fluorescence lifetime imaging can be used for label-free measurements of the metabolic states of cells within the living animal.
活体显微镜(IVM)是一种成像工具,能够在活体动物的组织中检测到亚细胞信号或代谢事件。然而,在高度散射的生物组织中进行成像具有挑战性,因为在获取的图像中,信号会随着深度的增加而衰减。深度相关的信号衰减是 IVM 的主要障碍,限制了可以获得有意义数据的深度。因此,通过 IVM 进行定量测量需要使用内部校准的方法,或者采用完全不同的信号评估方式。在这里,我们描述了如何利用基因编码生物传感器探针的比率成像来对细胞信号通路活性的变化进行定量测量。然后,我们描述了如何利用荧光寿命成像对活体动物细胞内的代谢状态进行无标记测量。