ATF4 Mediates Mitochondrial Unfolded Protein Response in Alveolar Epithelial Cells

• Published in: American journal of respiratory cell and molecular biology Vol. 63; no. 4; pp. 478 - 489
• Main Authors: Jiang, Dingyuan, Cui, Huachun, Xie, Na, Banerjee, Sami, Liu, Rui-Ming, Dai, Huaping, Thannickal, Victor J, Liu, Gang
• Format: Journal Article
• Language: English
• Published: United States American Thoracic Society 01.10.2020
• Subjects: Activating Transcription Factor 4 - metabolism; Alveolar Epithelial Cells - metabolism; Alveolar Epithelial Cells - physiology; Alveoli; Animals; Apoptosis - physiology; Cell Line; Cells; Endoplasmic reticulum; Endoplasmic Reticulum Stress - physiology; Epithelial cells; Humans; Idiopathic Pulmonary Fibrosis - metabolism; Idiopathic Pulmonary Fibrosis - physiopathology; Lung - metabolism; Lung diseases; Male; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondria - metabolism; Mitochondria - physiology; Original Research; Protein folding; Proteins; Signal Transduction - physiology; Unfolded Protein Response - physiology; ER stress; mitochondrial UPR; pulmonary fibrosis; alveolar epithelial cell
• ISSN: 1044-1549; 1535-4989
• DOI: 10.1165/rcmb.2020-0107OC

Although endoplasmic reticulum (ER) unfolded protein response (UPR ) is well known, mitochondrial unfolded protein response (UPR ) has not been recognized in alveolar epithelial cells. Furthermore, ER stress and mitochondrial dysfunction are frequently encountered in alveolar epithelial cells from an array of lung disorders. However, these two scenarios have been often regarded as separate mechanisms contributing to the pathogeneses. It is unclear whether there is interplay between these two phenomena or an integrator that couples these two signaling cascades in the stressed alveolar epithelial cells from those pathologies. In this study, we defined UPR in alveolar epithelial cells and identified ATF4 (activating transcription factor 4), but not ATF5, as the key regulator of UPR . We found that UPR led to UPR and mitochondrial dysfunction in an ATF4-dependent manner. In contrast, mitochondrial stresses did not activate UPR . We found that alveolar epithelial ATF4 and UPR were induced in aged mice with experimental pulmonary fibrosis as well as in patients with idiopathic pulmonary fibrosis. Finally, we found that the inducible expression of ATF4 in mouse alveolar epithelial cells aggravated pulmonary UPR , lung inflammation, body weight loss, and death upon bleomycin-induced lung injury. In conclusion, ER stress induces ATF4-dependent UPR and mitochondrial dysfunction, indicating a novel mechanism by which ER stress contributes to the pathogeneses of a variety of pulmonary disorders.