| First Author | Larson-Casey JL | Year | 2016 |
| Journal | Immunity | Volume | 44 |
| Issue | 3 | Pages | 582-596 |
| PubMed ID | 26921108 | Mgi Jnum | J:254662 |
| Mgi Id | MGI:6112347 | Doi | 10.1016/j.immuni.2016.01.001 |
| Citation | Larson-Casey JL, et al. (2016) Macrophage Akt1 Kinase-Mediated Mitophagy Modulates Apoptosis Resistance and Pulmonary Fibrosis. Immunity 44(3):582-596 |
| abstractText | Idiopathic pulmonary fibrosis (IPF) is a devastating lung disorder with increasing incidence. Mitochondrial oxidative stress in alveolar macrophages is directly linked to pulmonary fibrosis. Mitophagy, the selective engulfment of dysfunctional mitochondria by autophagasomes, is important for cellular homeostasis and can be induced by mitochondrial oxidative stress. Here, we show Akt1 induced macrophage mitochondrial reactive oxygen species (ROS) and mitophagy. Mice harboring a conditional deletion of Akt1 in macrophages (Akt1(-/-)Lyz2-cre) and Park2(-/-) mice had impaired mitophagy and reduced active transforming growth factor-beta1 (TGF-beta1). Although Akt1 increased TGF-beta1 expression, mitophagy inhibition in Akt1-overexpressing macrophages abrogated TGF-beta1 expression and fibroblast differentiation. Importantly, conditional Akt1(-/-)Lyz2-cre mice and Park2(-/-) mice had increased macrophage apoptosis and were protected from pulmonary fibrosis. Moreover, IPF alveolar macrophages had evidence of increased mitophagy and displayed apoptosis resistance. These observations suggest that Akt1-mediated mitophagy contributes to alveolar macrophage apoptosis resistance and is required for pulmonary fibrosis development. |
