Publications by authors named "Rebecca B Wilkerson"

Extracellular vesicles (EVs) participate in cell-to-cell communication and contribute toward homeostasis under physiological conditions. But EVs can also contribute toward a wide array of pathophysiology like cancer, sepsis, sickle cell disease, and thrombotic disorders. COVID-19 infected patients are at an increased risk of aberrant coagulation, consistent with elevated circulating levels of ultra-high molecular weight VWF multimers, D-dimer and procoagulant EVs.

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Article Synopsis
  • Sickle cell anemia and β-thalassemia intermedia are genetically different blood disorders that both increase the risk of pulmonary hypertension, with various underlying mechanisms contributing to this condition.
  • Both conditions exhibit similar issues like hemolysis and iron overload, prompting research on common characteristics in heart and lung function associated with their pulmonary hypertension.
  • The study found that while there are shared traits between the two diseases, there are also key differences in iron metabolism, leading to unique features in their pulmonary hypertension, suggesting potential pathways for targeted treatments.
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Trisomy 21 (T21) causes Down syndrome (DS), affecting immune and neurological function by ill-defined mechanisms. Here we report a large metabolomics study of plasma and cerebrospinal fluid, showing in independent cohorts that people with DS produce elevated levels of kynurenine and quinolinic acid, two tryptophan catabolites with potent immunosuppressive and neurotoxic properties, respectively. Immune cells of people with DS overexpress IDO1, the rate-limiting enzyme in the kynurenine pathway (KP) and a known interferon (IFN)-stimulated gene.

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Arctic ground squirrels provide a unique model to investigate metabolic responses to hibernation in mammals. During winter months these rodents are exposed to severe hypothermia, prolonged fasting, and hypoxemia. In the light of their role in oxygen transport/off-loading and owing to the absence of nuclei and organelles (and thus de novo protein synthesis capacity), mature red blood cells have evolved metabolic programs to counteract physiological or pathological hypoxemia.

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