Publications by authors named "Maria L Klement"

Article Synopsis
  • - The study focuses on the role of CD4 T cells that respond to low-density lipoprotein (LDL), which contributes to atherosclerotic cardiovascular disease, exploring how these T cells can have a protective effect rather than a negative one.
  • - Researchers created a specific mouse model to investigate the immune response to LDL, finding that certain T cells promoted the activation of B cells, resulting in the production of antibodies that help clear LDL from the body.
  • - The findings suggest that the immune reaction to LDL can lead to three beneficial outcomes: enhanced clearance of LDL, increased cholesterol excretion in feces, and reduced inflammation in blood vessels, providing insights for developing potential therapies.
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Background: Increased inflammatory activity destabilizes the atherosclerotic lesion and may lead to atherothrombosis and symptomatic cardiovascular disease. Co-stimulatory molecules, such as CD137, are key regulators of inflammation, and CD137 activity regulates inflammation in experimental atherosclerosis. Here, we hypothesized that CD137 activation promotes carotid artery inflammation and atherothrombosis.

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The human pathogen Mycoplasma pneumoniae has a very small genome but with many yet not identified gene functions, e.g. for membrane lipid biosynthesis.

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In the prokaryote Acholeplasma laidlawii, membrane bilayer properties are sensed and regulated by two interface glycosyltransferases (GTs), synthesizing major nonbilayer- (alMGS GT) and bilayer-prone glucolipids. These enzymes are of similar structure, as many soluble GTs, but are sensitive to lipid charge and curvature stress properties. Multivariate and bioinformatic sequence analyses show that such interface enzymes, in relation to soluble ones of similar fold, are characterized by high cationic charge, certain distances between small and cationic amino acids, and by amphipathic helices.

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