
Pulmonary microvascular endothelial cells, vital for lung gas exchange, heavily rely on glycolysis, preferring glucose over fructose. The study have unveiled that 6-Phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 (PFKFB3), a key glycolytic enzyme, plays a crucial role. PFKFB3 inhibits fructose metabolism, as demonstrated by improved survival of PFKFB3 knockout cells in fructose-rich, hypoxic conditions. This discovery sheds light on the control of glycolysis substrate selection and may advance our understanding of lung endothelial cell metabolism during respiratory failure. Pneumonia patients in ICU also exhibited increased fructose levels in BAL fluid.
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