In Vivo Imaging of Tracheal Epithelial Cells in Mice during Airway Regeneration

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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.
Publisher
AMER THORACIC SOC
Issue Date
2012-12
Language
English
Article Type
Article
Keywords

STEM-CELLS; LUNG; EXPRESSION; PROMOTER

Citation

AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, v.47, no.6, pp.864 - 868

ISSN
1044-1549
DOI
10.1165/rcmb.2012-0164OC
URI
http://hdl.handle.net/10203/174955
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