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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Zirlik, A; Lutgens, E.
An inflammatory link in atherosclerosis and obesity. Co-stimulatory molecules.
HAMOSTASEOLOGIE. 2015; 35(3): 272-278. Doi: 10.5482/HAMO-14-12-0079
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Führende Autor*innen der Med Uni Graz
Zirlik Andreas
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Abstract:
Atherosclerosis and obesity-induced metabolic dysfunction are lipid-driven inflammatory pathologies responsible for a major part of cardiovascular complications. Immune cell activation as well as interactions between the different immune cells is dependent on and controlled by a variety of co-stimulatory signals. These co-stimulatory signals can either aggravate or ameliorate the disease depending on the stage of the disease, the cell-types involved and the signal transduction cascades initiated. This review focuses on the diverse roles of the most established co-stimulatory molecules of the B7 and Tumor Necrosis Factor Receptor (TNFR) families, ie the CD28/CTLA4-CD80/CD86 and CD40L/CD40 dyads in the pathogenesis of atherosclerosis and obesity. In addition, we will explore their potential as therapeutic targets in both atherosclerosis and obesity.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Atherosclerosis - immunology
Cytokines - immunology
Humans -
Immunity, Innate - immunology
Inflammation Mediators - immunology
Lipid Metabolism - immunology
Models, Immunological -
Obesity - immunology
Signal Transduction - immunology

Find related publications in this database (Keywords)
Atherosclerosis
obesity
co-stimulation
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