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J Appl Physiol (June 21, 2007). doi:10.1152/japplphysiol.00160.2007
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Submitted on February 7, 2007
Accepted on June 20, 2007

Alveolar expansion imaged by optical sectioning microscopy

Carrie E Perlman1 and Jahar Bhattacharya1*

1 Departments of Medicine and Physiology and Cellular Biophysics, College of Physicians and Surgeons and St. Luke's-Roosevelt Hospital Center, Columbia University, New York, New York, United States

* To whom correspondence should be addressed. E-mail: jb39{at}columbia.edu.

During lung expansion, the pattern of alveolar perimeter distension is likely to be an important determinant of lung functions as for example, surfactant secretion. However, the segmental characteristics of alveolar perimeter distension remain unknown. Here, we applied real-time confocal microscopy in the isolated, perfused rat lung to determine the micromechanics of alveolar perimeter distension. To image the alveolar perimeter, we loaded alveolar epithelial cells with a fluorescent dye that we microinjected into the alveolus. Then, we viewed single alveoli in a 2 µm-thick optical section at a focal plane 20 µm deep to the pleural surface at baseline. In each alveolus, we identified 5-8 segments of the perimeter. For each segment, we determined length (Lseg) by means of image analysis. At baseline alveolar pressure (Palv) of 5 cmH2O, Lseg averaged 46 µm. We hyperinflated the lung to Palv of 20 cmH2O and identified the same optical section as referenced against morphologic landmarks. Hyperinflation increased mean Lseg by 14%. However, segment distension was heterogeneous even within the single alveolus. Further, distension was greater in alveolar type 1 than type 2 epithelial cells. These findings indicate that alveoli expand non-uniformly, suggesting that segments that distend the most might be preferred alveolar locations for injury in conditions associated with lung over-distension.




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