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首页> 外文期刊>The journal of asthma >Dll4 in the DCs isolated from OVA-sensitized mice is involved in Th17 differentiation inhibition by 1,25-dihydroxyvitamin D3 in vitro
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Dll4 in the DCs isolated from OVA-sensitized mice is involved in Th17 differentiation inhibition by 1,25-dihydroxyvitamin D3 in vitro

机译:从OVA致敏小鼠分离的DC中的Dll4参与体外1,25-二羟基维生素D3抑制Th17分化

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摘要

Introduction: T helper 17 cell (Th17) cells play an important role in neutrophilic asthma, and 1,25(OH)2D3 has been reported to modulate the proliferation and differentiation of T cells. In this study, we examined the effects of 1,25(OH)2D3 on the dendritic cell (DC)-mediated regulation of Th17differentiation from OVA-sensitized mice. Methods: DCs were isolated from ovalbumin-sensitized mouse spleens. Lipopolysaccharide (LPS) was administered to stimulate the DCs for 24h, and dexamethasone or 1,25(OH)2D3 was applied simultaneously. The expression of Notch ligand delta-like ligand 4 (Dll4) in the DCs was detected in each group. All the groups of treated DCs were co-cultured with T cells, and Dll4 was inhibited in these groups. After 24h, Th17 and Treg cell differentiation and the IL-17A levels were measured. Results: Dll4 expression was increased in LPS-treated DCs compared with the control group (p=0.05), resulting in increased Th17 cell differentiation (p=0.002). Treatment with 1,25(OH)2D3 inhibited the Dll4 expression(p=0.04) and decreased Th17 cell differentiation (p=0.001) in DCs that was induced by LPS. Directly inhibiting Dll4 reduced Th17 cell differentiation, and Th17 cell differentiation was not further inhibited by 1,25(OH)2D3 once Dll4 was blocked. Conclusions: These result suggest that Dll4 in the DCs isolated from OVA-sensitized mice is involved in Th17 differentiation inhibition by 1,25(OH)2D3.
机译:简介:T辅助细胞17(Th17)细胞在嗜中性哮喘中起重要作用,据报道1,25(OH)2D3可以调节T细胞的增殖和分化。在这项研究中,我们检查了1,25(OH)2D3对OVA致敏小鼠的树突状细胞(DC)介导的Th17分化调控的影响。方法:从卵清蛋白致敏的小鼠脾脏中分离DC。给予脂多糖(LPS)刺激DC 24h,并同时应用地塞米松或1,25(OH)2D3。在每组中检测DC中Notch配体δ样配体4(Dll4)的表达。将所有治疗的DC组与T细胞共培养,并且在这些组中Dll4被抑制。 24小时后,测量Th17和Treg细胞分化以及IL-17A水平。结果:与对照组相比,LPS处理的DC中Dll4表达增加(p = 0.05),导致Th17细胞分化增加(p = 0.002)。 1,25(OH)2D3处理抑制了LPS诱导的DC中Dll4的表达(p = 0.04),并降低了Th17细胞分化(p = 0.001)。直接抑制Dll4会降低Th17细胞的分化,一旦Dll4被阻断,则1,25(OH)2D3不会进一步抑制Th17细胞的分化。结论:这些结果表明,从OVA致敏小鼠分离的DC中的Dll4参与了1,25(OH)2D3抑制Th17分化。

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