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CFTR in alveolar type 1 cells contributes to lung liquid secretion and host defense
Sayahi Suthakaran, Sonya Homami, Deebly Chavez, Stephanie Tang, Sarah K.L. Moore, Chaya Sussman, Jimmy Zhang, Clemente J. Britto, Alice Prince, Alison J. May, Jaymin J. Kathiriya, Jaime L. Hook
Sayahi Suthakaran, Sonya Homami, Deebly Chavez, Stephanie Tang, Sarah K.L. Moore, Chaya Sussman, Jimmy Zhang, Clemente J. Britto, Alice Prince, Alison J. May, Jaymin J. Kathiriya, Jaime L. Hook
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Research Article Cell biology Infectious disease Pulmonology

CFTR in alveolar type 1 cells contributes to lung liquid secretion and host defense

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Abstract

CFTR in the lung epithelium contributes to the secretion of a surface liquid layer that is essential to lung homeostasis and defense. The understanding of how liquid is secreted in the lung is derived largely from studies of the airway epithelium. Comparatively little is known about liquid secretion mechanisms in the alveolar epithelium, including its cellular source. To define which cell type drives alveolar liquid secretion, we generated transgenic mice that expressed a Cftr-null allele in alveolar type 1 (AT1) cells, type 2 (AT2) cells, or both, then viewed liquid secretion in live alveoli using confocal microscopy of isolated, perfused lungs. Our findings show that liquid secretion was blocked in alveoli of all 3 transgenic mice, indicating that both AT1 and AT2 cells contribute to alveolar liquid secretion. Cftr-null expression in AT1 cells also blocked the secretion-mediated clearance of small particle and bacterial clusters from alveolar walls, indicating that AT1 cell CFTR contributes to alveolar defense. Together, these findings show alveolar liquid secretion depends on both AT1 and AT2 cell CFTR, and that CFTR in AT1 cells — a cell type not traditionally considered in liquid secretion mechanisms or CFTR-related lung diseases — contributes to lung liquid dynamics and host defense.

Authors

Sayahi Suthakaran, Sonya Homami, Deebly Chavez, Stephanie Tang, Sarah K.L. Moore, Chaya Sussman, Jimmy Zhang, Clemente J. Britto, Alice Prince, Alison J. May, Jaymin J. Kathiriya, Jaime L. Hook

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Figure 1

Alveolar epithelial cell type-specificity of GFP expression.

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Alveolar epithelial cell type-specificity of GFP expression.
(A) The ill...
(A) The illustration shows the experimental design of confocal imaging studies of live, intact, perfused lungs of transgenic mice. (B) Confocal images show plasma membrane GFP (cyan) and TdTomato (magenta) fluorescence in live lungs of mice of the indicated genotype. Dashed squares show locations of the high power views shown in the third and fourth columns. Closed arrowheads point out AT1 cell fluorescence, which is GFP+ (cyan) and distinct from neighboring TdTomato+ (magenta) endothelial cells only in AT1-CFTRnull-GFP and AT2-AT1-CFTRnull-GFP mice. Open arrowheads show plasma membrane fluorescence of AT2 cells, which is GFP+ (cyan) only in AT2-CFTRnull-GFP and AT2-AT1-CFTRnull-GFP mice. In the fourth column, cytosolic fluorescence of lysotracker green (LTG) delineates lamellar bodies (LB) and confirms AT2 cell identity. In the third row, arrows show example AT2 cells in an AT2-AT1-CFTRnull-GFP mouse. Air, airspace; ves, microvessel lumen. Scale bars: 100 (first and second columns), 3 (third columns), and 5 (fourth columns) μm. Images were replicated in lungs of 3 mice per genotype. Note, in the fourth column, both LTG and GFP are pseudocolored cyan.

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