Title: Restoration of SIRT3 gene expression by airway delivery resolves age-associated persistent lung fibrosis in mice.
Authors: Rehan, Mohammad; Kurundkar, Deepali; Kurundkar, Ashish R; Logsdon, Naomi J; Smith, Samuel R; Chanda, Diptiman; Bernard, Karen; Sanders, Yan Y; Deshane, Jessy S; Dsouza, Kevin G; Rangarajan, Sunad; Zmijewski, Jaroslaw W; Thannickal, Victor J
Published In Nat Aging, (2021 Feb)
Abstract: Aging is a risk factor for progressive fibrotic disorders involving diverse organ systems, including the lung. Idiopathic pulmonary fibrosis, an age-associated degenerative lung disorder, is characterized by persistence of apoptosis-resistant myofibroblasts. In this report, we demonstrate that sirtuin-3 (SIRT3), a mitochondrial deacetylase, is downregulated in lungs of IPF human subjects and in mice subjected to lung injury. Over-expression of the SIRT3 cDNA via airway delivery restored capacity for fibrosis resolution in aged mice, in association with activation of the forkhead box transcription factor, FoxO3a, in fibroblasts, upregulation of pro-apoptotic members of the Bcl-2 family, and recovery of apoptosis susceptibility. While transforming growth factor-β1 reduced levels of SIRT3 and FoxO3a in lung fibroblasts, cell non-autonomous effects involving macrophage secreted products were necessary for SIRT3-mediated activation of FoxO3a. Together, these findings reveal a novel role of SIRT3 in pro-resolution macrophage functions that restore susceptibility to apoptosis in fibroblasts via a FoxO3a-dependent mechanism.
PubMed ID: 34386777
MeSH Terms: Animals; Fibrosis; Gene Expression; Humans; Idiopathic Pulmonary Fibrosis*/metabolism; Lung/metabolism; Mice; Sirtuin 3*/genetics