Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Wolf, D; Jehle, F; Ortiz Rodriguez, A; Dufner, B; Hoppe, N; Colberg, C; Lozhkin, A; Bassler, N; Rupprecht, B; Wiedemann, A; Hilgendorf, I; Stachon, P; Willecke, F; Febbraio, M; von zur Muhlen, C; Binder, CJ; Bode, C; Zirlik, A; Peter, K.
CD40L deficiency attenuates diet-induced adipose tissue inflammation by impairing immune cell accumulation and production of pathogenic IgG-antibodies.
PLOS ONE. 2012; 7(3): e33026-e33026. Doi: 10.1371/journal.pone.0033026 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Zirlik Andreas
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Adipose tissue inflammation fuels the metabolic syndrome. We recently reported that CD40L--an established marker and mediator of cardiovascular disease--induces inflammatory cytokine production in adipose cells in vitro. Here, we tested the hypothesis that CD40L deficiency modulates adipose tissue inflammation in vivo. WT or CD40L(-/-) mice consumed a high fat diet (HFD) for 20 weeks. Inflammatory cell recruitment was impaired in mice lacking CD40L as shown by a decrease of adipose tissue macrophages, B-cells, and an increase in protective T-regulatory cells. Mechanistically, CD40L-deficient mice expressed significantly lower levels of the pro-inflammatory chemokine MCP-1 both, locally in adipose tissue and systemically in plasma. Moreover, levels of pro-inflammatory IgG-antibodies against oxidized lipids were reduced in CD40L(-/-) mice. Also, circulating low-density lipoproteins and insulin levels were lower in CD40L(-/-) mice. However, CD40L(-/-) mice consuming HFD were not protected from the onset of diet-induced obesity (DIO), insulin resistance, and hepatic steatosis, suggesting that CD40L selectively limits the inflammatory features of diet-induced obesity rather than its metabolic phenotype. Interestingly, CD40L(-/-) mice consuming a low fat diet (LFD) showed both, a favorable inflammatory and metabolic phenotype characterized by diminished weight gain, improved insulin tolerance, and attenuated plasma adipokine levels. We present the novel finding that CD40L deficiency limits adipose tissue inflammation in vivo. These findings identify CD40L as a potential mediator at the interface of cardiovascular and metabolic disease.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Autoantibodies - blood
Autoantibodies - immunology
B-Lymphocyte Subsets - immunology
B-Lymphocyte Subsets - metabolism
CD40 Ligand - deficiency
CD40 Ligand - immunology
Chemokines - genetics
Diet - adverse effects
Energy Metabolism - genetics
Fatty Liver - genetics
Gene Expression Regulation -
Immunoglobulin G - blood
Immunoglobulin G - immunology
Insulin Resistance - genetics
Lipid Metabolism -
Lipids - immunology
Male -
Mice -
Mice, Inbred C57BL -
Mice, Knockout -
Obesity - etiology
Oxidation-Reduction -
Panniculitis - etiology
Panniculitis - genetics
Panniculitis - immunology

© Med Uni Graz Impressum