Vitamin D reduces the inflammatory response and restores glucose uptake in adipocytes

被引:154
作者
Marcotorchino, Julie [2 ]
Gouranton, Erwan [2 ]
Romier, Beatrice [2 ]
Tourniaire, Franck [2 ]
Astier, Julien [2 ]
Malezet, Christiane [2 ]
Amiot, Marie-Josephe [2 ]
Landrier, Jean-Francois [1 ,2 ]
机构
[1] Aix Marseille Univ, INRA, INSERM 1062, Fac Med,UMR 1260, F-13385 Marseille 5, France
[2] INSERM, Nutr Obes & Risk Thrombosis UMR1062, Marseille, France
关键词
Adipocytes; Glucose uptake; Inflammation; Interleukins; Vitamin D;
D O I
10.1002/mnfr.201200383
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
Scope Obesity is strongly associated with low-grade inflammation, notably due to an overproduction of proinflammatory markers by adipose tissue and adipocytes as well as a vitamin D deficiency. Whether these problems are interrelated has not been clearly established. Methods and results In the present report, decreases in the levels of inflammatory markers such as IL-6, MCP-1, and IL-1 beta (mRNA and protein level) in human adipocytes and in 3T3-L1 adipocytes were observed after 1,25-dihydroxyvitamin D3 (1,25-(OH)2D3) treatment. Such treatment also decreased the expression of the TNF-alpha-mediated proinflammatory marker in 3T3-L1 and human adipocytes. A similar effect was observed in adipocyte-macrophage co-culture systems in which 1,25-(OH)2D3 decreased proinflammatory marker expression under basal and TNF-alpha-stimulated conditions. The involvement of VDR and NF-kappa B was confirmed in these regulations. Incubation with 1,25-(OH)2D3 also resulted in the dephosphorylation of p38, which is linked to the transcriptional induction of several Dusp family members. Functional consequences of the 1,25-(OH)2D3 treatment on glucose uptake and AKT phosphorylation were observed. Conclusion The improvement of both proinflammatory status and glucose uptake in adipocytes under 1,25-(OH)2D3 effect suggests that low-grade inflammation could be linked to vitamin D deficiency. This observation offers new perspectives in the context of obesity and associated physiopathological disorders.
引用
收藏
页码:1771 / 1782
页数:12
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