Publications by authors named "S G Bourgoin"

Article Synopsis
  • - Neutrophils are key immune cells that respond first to infections and they utilize various metabolic pathways, including glycolysis, fatty acid oxidation, and oxidative phosphorylation, to carry out their functions beyond just glycolysis.
  • - Their metabolism changes from using fatty acids in immature neutrophils to glycolysis in mature ones, and this shift is influenced by the surrounding tissue environment, including nutrient availability and inflammation.
  • - Disruptions in neutrophil metabolism can impair essential immune functions, linking these changes to diseases like antiphospholipid syndrome and COVID-19, with potential interventions targeting metabolic regulators like AMPK and mTOR for treatment.
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In phagocytes, cytoskeletal and membrane remodeling is finely regulated at the phagocytic cup. Various smaFll G proteins, including those of the Arf family, control these dynamic processes. Human neutrophils express AGAP2, an Arf GTPase activating protein (ArfGAP) that regulates endosomal trafficking and focal adhesion remodeling.

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Synovial fluids from rheumatoid and psoriatic arthritis patients have high levels of PLA1A. The current study was to understand PLA1A functions in the pathophysiology of rheumatic diseases. We generated Pla1a−/− mice to assess their phenotype and the impact of PLA1A deficiency on the development of mannan-induced psoriatic arthritis (MIP).

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Background: Extracellular vesicles (EVs) released by blood cells have proinflammation and procoagulant action. Patients with systemic lupus erythematosus (SLE) present high vascular inflammation and are prone to develop cardiovascular diseases. Therefore, we postulated that the EV populations found in blood, including platelet EVs (PEVs) and red blood cell EVs (REVs), are associated with SLE disease activity and SLE-associated cardiovascular accidents.

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Lysophosphatidylserine (lysoPS) is known to regulate immune cell functions. Phospholipase A1 member A (PLA1A) can generate this bioactive lipid through hydrolysis of sn-1 fatty acids on phosphatidylserine (PS). PLA1A has been associated with cancer metastasis, asthma, as well as acute coronary syndrome.

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