Previous work showed that lung injury activates a local tissue angiotensin system in pulmonary alveolar epithelial cells (AECs) and demonstrated that de novo synthesis of angiotensin (ANG) II is required for AEC apoptosis and subsequent lung fibrosis in animal models. An important component of this system that has not been studied well is angiotensin converting enzyme-2 (ACE-2), a carboxypeptidase that degrades ANGII to form ANG1-7, a heptapeptide that blocks ANGII action. This proposal is designed to begin elucidating the function(s) of ACE-2 and ANG1-7 in AEC survival in the context of lung fibrogenesis, and to begin defining the mechanisms by which ACE-2 is downregulated in experimental lung fibrosis.
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