Yes-associated Protein Induces Age-dependent Inflammatory Signaling in the Pulmonary Endothelium

Abstract Acute Lung Injury (ALI) causes the highly lethal Acute Respiratory Distress Syndrome (ARDS) in children and adults, for which therapy is lacking. Children with Pediatric ARDS (PARDS) have a mortality rate that is about half of adults with ARDS. Improved ALI measures can be reproduced in rodent models with juvenile animals, suggesting that physiologic differences may underlie these outcomes. Here, we show that pneumonia-induced ALI caused inflammatory signaling in the endothelium of adult mice which depended on Yes-associated protein (YAP). This signaling was not present in 21-day-old weanling mice. Transcriptomic analysis of lung endothelial responses revealed nuclear factor kappa-B (NF-κB) as significantly increased with ALI in adult versus weanling mice. Blockade of YAP signaling protected against inflammatory response, hypoxemia, and NF-κB nuclear translocation in response to Pseudomonas aeruginosa pneumonia in adult mice. Our results demonstrate an important signaling cascade in the lung endothelium of adult mice that is not present in weanlings. We suggest other pathways may also exhibit age-dependent signaling, which would have important implications for ARDS therapeutics in the adult and pediatric age groups. Competing Interest Statement The authors have declared no competing interest. Footnotes Conflict of interest statement: The authors have declared that no conflict of interest exists. Figures 3 and 4 revised. Experiments were repeated with solely the use of YAP-targeted siRNA. Taz-targeted siRNA data were not included. https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE291989