Publications by authors named "Quentin Gex"

Introduction: Metabolic alterations are recognized as key features of kidney injury, but their causal role in kidney repair remains debatable. Here, we investigate the role of phosphoenolpyruvate carboxykinase 1 (PCK1), an enzyme involved in gluconeogenesis and cataplerosis (removal of tricarboxylic acid (TCA) cycle intermediates from the mitochondrial matrix) in kidney disease progression.

Methods: We used mice with kidney tubular cell-specific deletion or overexpression of the PCK1 enzyme, and different models of kidney injury such as ischemia-reperfusion injury or cis-platin-induced nephropathy.

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  • Maternal obesity has been linked to a higher risk of hepatocellular carcinoma (HCC) in offspring, and this study explores the mechanisms behind this connection.
  • Female mice were fed either a high-fat diet or a normal diet, and their offspring were studied for liver health and tumor development after being induced with HCC.
  • Results showed that offspring from obese mothers had more liver diseases and tumors, linked to changes in gut microbiome, suggesting that gut health may play a critical role in developing these conditions.
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Background And Aims: Non-alcoholic fatty liver disease (NAFLD) is one of the leading cause of hepatocellular carcinoma (HCC). This association is supported by the translocation of bacteria products into the portal system, which acts on the liver through the gut-liver axis. We hypothesize that portosystemic shunting can disrupt this relationship, and prevent NAFLD-associated HCC.

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  • PCK1 (phosphoenolpyruvate carboxykinase 1) is a key enzyme in kidney cells that helps convert oxaloacetate to phosphoenolpyruvate and plays a role in maintaining metabolic processes such as gluconeogenesis and ammoniagenesis.
  • Deleting PCK1 in kidney-specific knockout mice led to metabolic issues including hyperchloremic metabolic acidosis and altered metabolism, causing kidney injury and decreased ATP production.
  • Enhancing PCK1 expression during chronic kidney disease improved renal function, highlighting its importance for acid-base balance, energy production, and overall tubular health.
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Nonalcoholic steatohepatitis (NASH) can lead to hepatocellular carcinoma (HCC). Although immunotherapy is used as first-line treatment for advanced HCC, the impact of NASH on anticancer immunity is only partially characterized. We assessed the tumor-specific T cell immune response in the context of NASH.

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  • * Researchers conducted genomic analysis and created a mouse model to explore how maternal obesity affects liver gene expression, identifying several dysregulated pathways and genes connected to liver disease.
  • * The study found a significant increase in liver disease risk and liver enzyme levels in female offspring of obese mothers, while male offspring showed greater liver fibrosis, highlighting the potential long-term health threats posed by maternal obesity.
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Intraportal islet transplantation is plagued by an acute destruction of transplanted islets. Amongst the first responders, NK cells and macrophages harbour an activating receptor, NKG2D, recognizing ligands expressed by stressed cells. We aimed to determine whether islet NKG2D ligand expression increases with culture time, and to analyse the impact of antibody-induced NKG2D blockade in islet transplantation.

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Hypothermic and normothermic ex vivo liver perfusions promote organ recovery after donation after circulatory death (DCD). We tested whether these perfusions can reduce the risk of hepatocellular carcinoma (HCC) recurrence in a 1h-DCD syngeneic transplantation model, using Fischer F344 rats. DCD grafts were machine perfused for 2h with hypothermic perfusion (HOPE) or normothermic perfusion (NORMO), and transplanted.

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Remote ischaemic preconditioning (RIPC), which is the intermittent interruption of blood flow to a site distant from the target organ, is known to improve solid organ resistance to ischaemia-reperfusion injury. This procedure could be of interest in islet transplantation to mitigate hypoxia-related loss of islet mass after isolation and transplantation. Islets isolated from control or RIPC donors were analyzed for yield, metabolic activity, gene expression and high mobility group box-1 (HMGB1) content.

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Background & Aims: A major limitation in the field of liver transplantation is the shortage of transplantable organs. Chimeric animals carrying human tissue have the potential to solve this problem. However, currently available chimeric organs retain a high level of xenogeneic cells, and the transplantation of impure organs needs to be tested.

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Because of the wide availability of genetically modified animals, mouse orthotopic liver transplantation is often preferred over rat liver transplantation. We present a simplified mouse liver transplantation technique and compare transplantation outcomes with versus without hepatic artery anastomosis. Instruments for liver implantation were designed and printed with a 3-dimensional (3D) printer.

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