Department of Anatomy and Molecular Histology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Shimokato, Chuo City, Yamanashi, Japan.
Histochem Cell Biol. 2012 Feb;137(2):137-51. doi: 10.1007/s00418-011-0892-1. Epub 2011 Nov 29.
Light microscopic imaging of blood vessels and distribution of serum proteins is essential to analyze hemodynamics in living animal lungs under normal respiration or respiratory diseases. In this study, to demonstrate dynamically changing morphology and immunohistochemical images of their living states, "in vivo cryotechnique" (IVCT) combined with freeze-substitution fixation was applied to anesthetized mouse lungs. By hematoxylin-eosin staining, morphological features, such as shapes of alveolar septum and sizes of alveolar lumen, reflected their respiratory conditions in vivo, and alveolar capillaries were filled with variously shaped erythrocytes. Albumin was usually immunolocalized in the capillaries, which was confirmed by double-immunostaining for aquaporin-1 of endothelium. To capture accurate time-courses of blood flow in peripheral pulmonary alveoli, glutathione-coated quantum dots (QDs) were injected into right ventricles, and then IVCT was performed at different time-points after the QD injection. QDs were localized in most arterioles and some alveolar capillaries at 1 s, and later in venules at 2 s, reflecting a typical blood flow direction in vivo. Three-dimensional QD images of microvascular networks were reconstructed by confocal laser scanning microscopy. It was also applied to lungs of acute pulmonary hypertension mouse model. Erythrocytes were crammed in blood vessels, and some serum components leaked into alveolar lumens, as confirmed by mouse albumin immunostaining. Some separated collagen fibers and connecting elastic fibers were still detected in edematous tunica adventitia near terminal bronchioles. Thus, IVCT combined with histochemical approaches enabled us to capture native images of dynamically changing structures and microvascular hemodynamics of living mouse lungs.
观察血管和血清蛋白分布的光镜成像对于分析正常呼吸或呼吸疾病状态下活体动物肺部的血液动力学至关重要。在这项研究中,为了展示其活体状态下形态和免疫组织化学图像的动态变化,我们将“活体冷冻技术”(IVCT)与冷冻置换固定相结合应用于麻醉小鼠的肺部。通过苏木精-伊红染色,肺泡隔的形状和肺泡腔的大小等形态特征反映了它们在体内的呼吸状态,肺泡毛细血管中充满了各种形状的红细胞。白蛋白通常在毛细血管中免疫定位,这通过内皮细胞水通道蛋白-1 的双重免疫染色得到证实。为了准确捕捉周围肺肺泡血流的时间过程,将谷胱甘肽包覆的量子点(QD)注入右心室,然后在 QD 注射后的不同时间点进行 IVCT。在 1 秒时,QD 定位于大多数小动脉和一些肺泡毛细血管中,在 2 秒时则定位于小静脉中,反映了体内典型的血流方向。通过共聚焦激光扫描显微镜对微血管网络的三维 QD 图像进行重建。我们还将其应用于急性肺动脉高压小鼠模型的肺部。血管中挤满了红细胞,一些血清成分渗漏到肺泡腔中,通过小鼠白蛋白免疫染色得到证实。在终末细支气管附近的水肿血管外膜中,仍可检测到一些分离的胶原纤维和连接的弹性纤维。因此,IVCT 结合组织化学方法使我们能够捕获活体小鼠肺部动态变化结构和微血管血液动力学的天然图像。