Abstract
The lung is a branched tubular network with two distinct compartments--the proximal conducting airways and the peripheral gas exchange region--separated by a discrete boundary termed the bronchoalveolar duct junction (BADJ). Here we image the developing mouse lung in three-dimensions (3D) and show that two nested developmental waves demarcate the BADJ under the control of a global hormonal signal. A first wave of branching morphogenesis progresses throughout embryonic development, generating branches for both compartments. A second wave of conducting airway differentiation follows the first wave but terminates earlier, specifying the proximal compartment and setting the BADJ. The second wave is terminated by a glucocorticoid signalling: premature activation or loss of glucocorticoid signalling causes a proximal or distal shift, respectively, in BADJ location. The results demonstrate a new mechanism of boundary formation in complex, 3D organs and provide new insights into glucocorticoid therapies for lung defects in premature birth.
Publication types
-
Research Support, N.I.H., Extramural
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Actins / metabolism
-
Animals
-
Bronchi / anatomy & histology
-
Bronchi / embryology*
-
Bronchi / metabolism
-
Cadherins / metabolism
-
Cell Differentiation
-
Glucocorticoids / metabolism
-
Imaging, Three-Dimensional
-
Immunohistochemistry
-
Intercellular Signaling Peptides and Proteins
-
Lung / embryology
-
Lung / metabolism
-
Mice
-
Morphogenesis
-
Peptides / metabolism
-
Pulmonary Alveoli / anatomy & histology
-
Pulmonary Alveoli / embryology*
-
Pulmonary Alveoli / metabolism
-
Pulmonary Surfactant-Associated Protein C
-
Receptor for Advanced Glycation End Products
-
Receptors, Immunologic / metabolism
-
SOXB1 Transcription Factors / metabolism
-
Signal Transduction
-
Uteroglobin / metabolism
Substances
-
Actins
-
Cadherins
-
Glucocorticoids
-
Intercellular Signaling Peptides and Proteins
-
Peptides
-
Pulmonary Surfactant-Associated Protein C
-
Receptor for Advanced Glycation End Products
-
Receptors, Immunologic
-
SOXB1 Transcription Factors
-
Scgb1a1 protein, mouse
-
Sftpc protein, mouse
-
Sox2 protein, mouse
-
Uteroglobin