Harvard Medical School, Massachusetts General Hospital, Boston, MA, USA.
Am J Respir Cell Mol Biol. 2012 Dec;47(6):864-8. doi: 10.1165/rcmb.2012-0164OC. Epub 2012 Sep 13.
Many human lung diseases, such as asthma, chronic obstructive pulmonary disease, bronchiolitis obliterans, and cystic fibrosis, are characterized by changes in the cellular composition and architecture of the airway epithelium. Intravital fluorescence microscopy has emerged as a powerful approach in mechanistic studies of diseases, but it has been difficult to apply this tool for in vivo respiratory cell biology in animals in a minimally invasive manner. Here, we describe a novel miniature side-view confocal probe capable of visualizing the epithelium in the mouse trachea in vivo at a single-cell resolution. We performed serial real-time endotracheal fluorescence microscopy in live transgenic reporter mice to view the three major cell types of the large airways, namely, basal cells, Clara cells, and ciliated cells. As a proof-of-concept demonstration, we monitored the regeneration of Clara cells over 18 days after a sulfur dioxide injury. Our results show that in vivo tracheal microscopy offers a new approach in the study of altered, regenerating, or metaplastic airways in animal models of lung diseases.
许多人类肺部疾病,如哮喘、慢性阻塞性肺疾病、闭塞性细支气管炎和囊性纤维化,其特征是气道上皮细胞的组成和结构发生变化。活体荧光显微镜已成为疾病机制研究的有力手段,但很难以微创的方式将该工具应用于动物体内的呼吸细胞生物学。在这里,我们描述了一种新型的微型侧视共聚焦探头,能够以单细胞分辨率对活体小鼠气管中的上皮进行成像。我们在活的转基因报告小鼠中进行了一系列实时气管内荧光显微镜检查,以观察大呼吸道的三种主要细胞类型,即基底细胞、克拉拉细胞和纤毛细胞。作为概念验证的演示,我们监测了二氧化硫损伤后 18 天克拉拉细胞的再生。我们的结果表明,活体气管显微镜为肺部疾病动物模型中气道改变、再生或化生的研究提供了一种新方法。