Effects of Vitamin D Supplementation on CD4+ T Cell Subsets and mTOR Signaling Pathway in High-Fat-Diet-Induced Obese Mice |
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Authors: | Jeong Hee An Da Hye Cho Ga Young Lee Min Su Kang So Jeong Kim Sung Nim Han |
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Affiliation: | 1.Department of Food and Nutrition, College of Human Ecology, Seoul National University, Seoul 08826, Korea; (J.H.A.); (D.H.C.); (G.Y.L.); (M.S.K.); (S.J.K.);2.Research Institute of Human Ecology, Seoul National University, Seoul 08826, Korea |
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Abstract: | Obesity is associated with an impaired balance of CD4+ T cell subsets. Both vitamin D and obesity have been reported to affect the mTOR pathway. In this study, we investigated the effects of vitamin D on CD4+ T cell subsets and the mTOR pathway. Ten-week-old male C57BL/6 mice were divided into four groups and fed diets with different fat (control or high-fat diets: CON or HFD) and vitamin D contents (vitamin D control or supplemented diets: vDC or vDS) for 12 weeks. T cells purified by negative selection were stimulated with anti-CD3/anti-CD28 mAbs and cultured for 48 h. The percentage of CD4+IL-17+ T cells was higher in the vDS than vDC groups. The CD4+CD25+Foxp3+ T cells percentage was higher in HFD than CON groups. The phospho-p70S6K/total-p70S6K ratio was lower in vDS than vDC, but the phospho-AKT/total-AKT ratio was higher in vDS than vDC groups. Hif1α mRNA levels were lower in vDS than vDC groups. These findings suggest HIF1α plays an important role in vitamin-D-mediated regulation of glucose metabolism in T cells, and dietary vitamin D supplementation may contribute to the maintenance of immune homeostasis by regulating the mTOR pathway in T cells. |
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Keywords: | CD4+ T cell, vitamin D supplementation, mTOR pathway, obesity, HIF1α |
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