Hall Stefan, Faridi Sufyan, Euodia Irene, Tanner Sophie, Chojnacki Andrew Krzysztof, Patel Kamala D, Zhou Juan, Lehmann Christian
Department of Physiology and Biophysics, Dalhousie University.
Department of Microbiology and Immunology, Dalhousie University.
J Vis Exp. 2022 Apr 6(182). doi: 10.3791/63733.
Intravital imaging of leukocyte-endothelial interactions offers valuable insights into immune-mediated disease in live animals. The study of acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) and other respiratory pathologies in vivo is difficult due to the limited accessibility and inherent motion artifacts of the lungs. Nonetheless, various approaches have been developed to overcome these challenges. This protocol describes a method for intravital fluorescence microscopy to study real-time leukocyte-endothelial interactions in the pulmonary microcirculation in an experimental model of ALI. An in vivo lung imaging system and 3-D printed intravital microscopy platform are used to secure the anesthetized mouse and stabilize the lung while minimizing confounding lung injury. Following preparation, widefield fluorescence microscopy is used to study leukocyte adhesion, leukocyte rolling, and capillary function. While the protocol presented here focuses on imaging in an acute model of inflammatory lung disease, it may also be adapted to study other pathological and physiological processes in the lung.
白细胞与内皮细胞相互作用的活体成像为深入了解活体动物免疫介导的疾病提供了有价值的见解。由于肺部的可及性有限以及固有的运动伪影,对急性肺损伤(ALI)/急性呼吸窘迫综合征(ARDS)和其他呼吸道疾病进行体内研究具有一定难度。尽管如此,人们已经开发出各种方法来克服这些挑战。本方案描述了一种在ALI实验模型中利用活体荧光显微镜研究肺微循环中白细胞与内皮细胞实时相互作用的方法。使用体内肺成像系统和3D打印的活体显微镜平台来固定麻醉的小鼠并稳定肺部,同时将混杂的肺损伤降至最低。制备完成后,利用宽视野荧光显微镜研究白细胞黏附、白细胞滚动和毛细血管功能。虽然此处介绍的方案主要聚焦于炎症性肺病急性模型中的成像,但它也可用于研究肺部的其他病理和生理过程。