Regulation of phagocyte NADPH oxydase activity by enzymes regulating glucose metabolism and S100A8/S100A9 heterocomplex : application to rheumatoid arthritis
type: Dataset
description: Rheumatoid Arthritis (RA) is caused by an inflammation of the synovial membrane leading to progressive joint destruction and deformation, related to the production NADPH oxidase related-reactive oxygen species (ROS) production. The phagocyte NADPH oxidase is a multi-protein complex formed by a catalytic core, i.e. the transmembrane cytochrome b558 and cytosolic regulators (p67phox, p47phox, p40phox and Rac1/2). We aimed at better analyzing the NADPH oxidase activation through the evaluation of the specificity of the interaction with 6PGDH or PFK2 and through the further analysis of the association with the S100A8/A9 heterocomplex. The RA-specific protein profiling was conducted in order to determine whether a PMN activation fingerprint could be revealed among RA specific proteins.Upon PMA stimulation, both 6PGDH and PFK2 co-imunoprecipitated with cytosolic factors p67phox, p47phox and p40phox. At the plasma membrane level, confocal microscopy experiments suggested a co-localization of either 6PGDH or PFK2 with the phagocyte NADPH oxidase in lipid rafts. 6PGDH enhanced the phagocyte NADPH oxidase activity by both improving the availability of cytosolic NADPH content and by increasing the affinity of the NADPH oxidase for its substrate. PFK2 also augmented the NADPH oxidase activity. PFK2 modulated the ATP concentration available for the phosphorylation of the phagocyte NADPH oxidase components and for the NDP Kinase related-Rac activation. The generation of truncated S100A8/S100A9 heterodimer chimera could reveal that the C-terminal region of S100A8 is involved in both the interaction and the activation of the phagocyte NADPH oxidase.In vivo, synovial fluid of RA patients was remarkably labelled with the PMN activation fingerprint. S100A8 and S100A9 proteins clearly distinguished RA synovial fluid from osteoarthritis and non RA-synovial fluids. An ectopic production of S100A8/S100A9 was shown in RA fibroblast like synoviocyte.In conclusion, 6PGDH, PFK2 and S100A8/A9 …
identifier: NNT: 2011GRENV074
issued: 2026-05-24T08:19:28.531935
language: fr
modified: 2026-05-24T08:19:28.531943
contact point: Organization
  fn: CCSD
keyword: 6-phosphofructokinase-26-phosphogluconate-dehydrogenase
keyword: infoeu-reposemanticsdoctoralthesis
keyword: nadph-oxidase
keyword: nadph-oxydase
keyword: polyarthrite-rhumatoide
keyword: polymorphonuclear-neutrophils
keyword: polynucleaires-neutrophiles
keyword: proteines-s100a8a96-phosphofructokinase-26-phosphogluconate-deshydrogenase
keyword: rheumatoid-arthritis
keyword: s100a8a9-proteins
keyword: sdvotlife-sciences-q-bioother-q-bioot
keyword: theses
landing page: https://theses.hal.science/tel-00680093

Regulation of phagocyte NADPH oxydase activity by enzymes regulating glucose metabolism and S100A8/S100A9 heterocomplex : application to rheumatoid arthritis
type: Distribution
format: HTML
issued: 2026-05-24T08:19:28.578065
modified: 2026-05-24T08:19:28.495788
access URL: https://theses.hal.science/tel-00680093

test_moissonnage_selune
type: Agent