High glucose levels increase influenza-associated damage to the pulmonary epithelial-endothelial barrier.
Katina D HulmeLimin YanRebecca J MarshallConor J BloxhamKyle R UptonSumaira Z HasnainHelle Bielefeldt-OhmannZhixuan LohKatharina RonacherKeng Yih ChewLinda A GalloKirsty R ShortPublished in: eLife (2020)
Diabetes mellitus is a known susceptibility factor for severe influenza virus infections. However, the mechanisms that underlie this susceptibility remain incompletely understood. Here, the effects of high glucose levels on influenza severity were investigated using an in vitro model of the pulmonary epithelial-endothelial barrier as well as an in vivo murine model of type II diabetes. In vitro we show that high glucose conditions prior to IAV infection increased virus-induced barrier damage. This was associated with an increased pro-inflammatory response in endothelial cells and the subsequent damage of the epithelial junctional complex. These results were subsequently validated in vivo. This study provides the first evidence that hyperglycaemia may increase influenza severity by damaging the pulmonary epithelial-endothelial barrier and increasing pulmonary oedema. These data suggest that maintaining long-term glucose control in individuals with diabetes is paramount in reducing the morbidity and mortality associated with influenza virus infections.
Keyphrases
- high glucose
- endothelial cells
- pulmonary hypertension
- inflammatory response
- type diabetes
- oxidative stress
- vascular endothelial growth factor
- glycemic control
- cardiovascular disease
- electronic health record
- mass spectrometry
- lipopolysaccharide induced
- immune response
- machine learning
- blood glucose
- high resolution
- insulin resistance
- toll like receptor
- deep learning