1. Enhanced ROS Production and Mitochondrial Metabolic Shifts in CD4 + T Cells of an Autoimmune Uveitis Model.
- Author
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Söth R, Hoffmann ALC, and Deeg CA
- Subjects
- Animals, Horses, Glucose metabolism, Horse Diseases metabolism, Horse Diseases immunology, Glycolysis, Oxygen Consumption, Fatty Acids metabolism, Oxidation-Reduction, Reactive Oxygen Species metabolism, Uveitis metabolism, Uveitis veterinary, Uveitis immunology, Uveitis pathology, CD4-Positive T-Lymphocytes metabolism, CD4-Positive T-Lymphocytes immunology, Mitochondria metabolism, Autoimmune Diseases metabolism, Autoimmune Diseases immunology, Disease Models, Animal
- Abstract
Equine recurrent uveitis (ERU) is a spontaneously occurring autoimmune disease and one of the leading causes of blindness in horses worldwide. Its similarities to autoimmune-mediated uveitis in humans make it a unique spontaneous animal model for this disease. Although many aspects of ERU pathogenesis have been elucidated, it remains not fully understood and requires further research. CD4
+ T cells have been a particular focus of research. In a previous study, we showed metabolic alterations in CD4+ T cells from ERU cases, including an increased basal oxygen consumption rate (OCR) and elevated compensatory glycolysis. To further investigate the underlying reasons for and consequences of these metabolic changes, we quantified reactive oxygen species (ROS) production in CD4+ T cells from ERU cases and compared it to healthy controls, revealing significantly higher ROS production in ERU-affected horses. Additionally, we aimed to define mitochondrial fuel oxidation of glucose, glutamine, and long-chain fatty acids (LCFAs) and identified significant differences between CD4+ T cells from ERU cases and controls. CD4+ T cells from ERU cases showed a lower dependency on mitochondrial glucose oxidation and greater metabolic flexibility for the mitochondrial oxidation of glucose and LCFAs, indicating an enhanced ability to switch to alternative fuels when necessary.- Published
- 2024
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