Modulation of monocyte hyperresponsiveness to TLR ligands by 1,25-dihydroxy-vitamin D3 from LADA and T2DM

被引:34
|
作者
Du, Tao [1 ]
Zhou, Zhi-Guang [1 ]
You, Shuo [1 ]
Huang, Gan [1 ]
Lin, Jian [1 ]
Yang, Lin [1 ]
Li, Xia [1 ]
Zhou, Wei-Dong [1 ]
Chao, Chen [1 ]
机构
[1] Cent S Univ, Xiangya Hosp 2, Ctr Diabet, Inst Metab & Endocrinol, Changsha 410011, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
1,25-Dihydroxy-vitamin D3; CD14; Toll-like receptor 2; Toll-like receptor 4; TOLL-LIKE RECEPTOR-2; INSULIN-RESISTANCE; DIABETES-MELLITUS; INNATE IMMUNITY; VITAMIN-D; EXPRESSION; OBESITY; MACROPHAGES; DISEASE;
D O I
10.1016/j.diabres.2008.09.046
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To investigate the differences of Toll-like receptors (TLRs) expression and response of monocyte and modulation of 1,25-dihydroxy-vitamin D3 on monocyte activity. Peripheral blood monocytes were collected from 23 healthy controls, 18 latent autoimmune diabetes in adults (LADA), and 22 type 2 diabetes mellitus (T2DM), respectively. CD14, TLR2 and TLR4 expression were analyzed. Moreover, the effect of 1,25-dihydroxy-vitamin D3 (1,25(OH)(2)D3) on monocyte response to lipoteichoic acid (LTA) and lipopolysaccharide (LPS) was evaluated in vitro by measuring phosphorylation level of NF-kappa B-p65 and associated cytokine production. Monocytes showed significantly higher surface CD14 expression from LADA compared with that from T2DM and controls, and high expression of TLR4 from LADA and T2DM than controls. After incubation with LPS or LTA, decreased surface expressions of CD14 were observed on monocytes from T2DM and controls, in contrast to the increased on monocytes from LADA. Activation of NF-kappa B and amounts of IL-1 beta and TNF-alpha production by stimulation with ligands significantly increased in LADA and T2DM, which was modulated by 1,25(OH)(2)D3 to similar level, as compared to controls. The modulation of 1,25(OH)(2)D3 on monocytes makes us to consider more potency of vitamin D3 as therapy in LADA and T2DM. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:208 / 214
页数:7
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