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- W2794554845 abstract "Inflammatory Arthritis is characterized by synovial proliferation, neovascularization and leukocyte extravasation leading to joint destruction and functional disability. Efficiency of oxygen supply to the synovium is poor due to the highly dysregulated synovial microvasculature. This along with the increased energy demands of activated infiltrating immune cells and inflamed resident cells leads to an hypoxic microenvironment and mitochondrial dysfunction. This favors an increase of reactive oxygen species, leading to oxidative damage which further promotes inflammation. In this adverse microenvironment synovial cells adapt to generate energy and switch their cell metabolism from a resting regulatory state to a highly metabolically active state which allows them to produce essential building blocks to support their proliferation. This metabolic shift results in the accumulation of metabolic intermediates which act as signaling molecules that further dictate the inflammatory response. Understanding the complex interplay between hypoxia-induced signaling pathways, oxidative stress and mitochondrial function will provide better insight into the underlying mechanisms of disease pathogenesis." @default.
- W2794554845 created "2018-04-06" @default.
- W2794554845 creator A5011749195 @default.
- W2794554845 creator A5017692535 @default.
- W2794554845 creator A5026167561 @default.
- W2794554845 creator A5087034199 @default.
- W2794554845 date "2018-09-01" @default.
- W2794554845 modified "2023-10-17" @default.
- W2794554845 title "Hypoxia, oxidative stress and inflammation" @default.
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