Deletion of Apoptosis Signal–Regulating Kinase–1 Prevents Ventilator-Induced Lung Injury in Mice

• DOI: 10.1165/rcmb.2011-0234oc
• Publication Date: 2011-11-04T03:09:01Z
• Authors: Patrudu S. Makena; Vijay K. Gorantla; Manik C. Ghosh; Lavanya Bezawada; Kathirvel Kandasamy; Louisa Balazs; Charlean L. Luellen; Karin E. Thompson; Kaushik Parthasar...; Hidenori Ichijo; Christopher M. Wa...; Scott E. Sinclair
• Keywords: Male; Mice, Knockout; 0303 health sciences; Ventilator-Induced Lung Injury; Apoptosis; Epithelial Cells; Hyperoxia; MAP Kinase Kinase Kinase 5; Enzyme Activation; Pulmonary Alveoli; Disease Models, Animal; Mice; 03 medical and health sciences; Animals; Cytokines; Female; Inflammation Mediators

Both hyperoxia and mechanical ventilation can independently cause lung injury. In combination, these insults produce accelerated and severe lung injury. We recently reported that pre-exposure to hyperoxia for 12 hours, followed by ventilation with large tidal volumes, induced significant lung injury and epithelial cell apoptosis compared with either stimulus alone. We also reported that such injury and apoptosis are inhibited by antioxidant treatment. In this study, we hypothesized that apoptosis signal-regulating kinase-1 (ASK-1), a redox-sensitive, mitogen-activated protein kinase kinase kinase, plays a role in lung injury and apoptosis in this model. To determine the role of ASK-1 in lung injury, the release of inflammatory mediators and apoptosis, attributable to 12 hours of hyperoxia, were followed by large tidal volume mechanical ventilation with hyperoxia. Wild-type and ASK-1 knockout mice were subjected to hyperoxia (Fi(O(2)) = 0.9) for 12 hours before 4 hours of large tidal mechanical ventilation (tidal volume = 25 μl/g) with hyperoxia, and were compared with nonventilated control mice. Lung injury, apoptosis, and cytokine release were measured. The deletion of ASK-1 significantly inhibited lung injury and apoptosis, but did not affect the release of inflammatory mediators, compared with the wild-type mice. ASK-1 is an important regulator of lung injury and apoptosis in this model. Further study is needed to determine the mechanism of lung injury and apoptosis by ASK-1 and its downstream mediators in the lung.