Publication | Open Access
Hypercholesterolemia Enhances T Cell Receptor Signaling and Increases the Regulatory T Cell Population
64
Citations
35
References
2017
Year
Lymphocyte DevelopmentT-regulatory CellImmunologyImmune RegulationRegulatory T CellsHyperlipidemiaCd4 T Cell ResponsesImmune DysregulationInflammationCholesterol-containing DietCell SignalingAtherosclerosisDyslipidemiaRegulatory T Cell BiologyLipid DisorderAutoimmune DiseaseAutoimmunityCell BiologyImmune Cell DevelopmentLipoprotein MetabolismCellular Immune ResponsePeripheral Treg CellsMedicineCell DevelopmentCholesterol Supplementation
Hypercholesterolemia promotes the inflammation against lipoproteins in atherosclerosis. Development of atherosclerosis is affected by the balance between pro-inflammatory effector T cells and anti-inflammatory regulatory T (Treg) cells. However, phenotype and function of T cell subpopulations in hypercholesterolemia remain to be investigated. Here, we found that cholesterol-containing diet increased the expression of the Treg cell lineage-defining transcription factor FoxP3 among thymocytes and splenocytes. Hypercholesterolemia elevated the FoxP3 expression level and population size of peripheral Treg cells, but did not prevent enhanced proliferation of stimulated T cells. Moreover, cholesterol supplementation in diet as well as in cell culture medium promoted T cell antigen receptor (TCR) signaling in CD4+ T cells. Our results demonstrate that hypercholesterolemia enhances TCR stimulation, Treg cell development as well as T cell proliferation. Thus, our findings may help to understand why hypercholesterolemia correlates with altered CD4+ T cell responses.
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