首页> 美国卫生研究院文献>Annals of the American Thoracic Society >Vitamin D Reduces Inflammation-induced Contractility and Remodeling of Asthmatic Human Airway Smooth Muscle
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Vitamin D Reduces Inflammation-induced Contractility and Remodeling of Asthmatic Human Airway Smooth Muscle

机译:维生素D减少炎症引起的收缩和哮喘人气道平滑肌重塑

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摘要

>Background: Although multiple clinical studies have found an association between vitamin D (Vit D) deficiency and asthma, a recent clinical study suggested lack of therapeutic effect of Vit D supplementation. Nonetheless, the mechanisms by which Vit D influences airway structure and function in the context of inflammation and asthma remains undefined. In this regard, Vit D effects on airway smooth muscle (ASM) are important, given the role of this cell type in the hypercontractility and remodeling. We assessed the mechanisms by which Vit D modulates the enhancing effects of proinflammatory cytokines tumor necrosis factor-α (TNF-α) and IL-13 on intracellular Ca2+ ([Ca2+]i) levels and remodeling in nonasthmatic versus asthmatic human ASM.>Methods: Human ASM was enzymatically isolated from surgical lung specimens of patients with clinically defined mild to moderate asthma versus no asthma. Cells were treated with 10 ng/ml TNF-α and 50 ng/ml IL-13 in the presence or absence of 100 nM calcitriol.>Measurements and Main Results: Interestingly, Vit D receptor (VDR) and retinoic X receptor-α levels were maintained, even increased, in subjects with asthma when treated with TNF-α and IL-13. Compared with untreated cells, calcitriol blunted the heightened effect of TNF-α on [Ca2+]i response to histamine in ASM. Calcitriol particularly blunted TNF-α and IL-13 effects on collagen and fibronectin deposition, especially in asthmatic ASM. Calcitriol stimulated VDR/retinoic X receptor dimerization and VDR activity even in subjects with asthma and with IL-13, highlighting retained functionality. Expression of Class I histone deacetylases 1–3 (HDAC) and overall HDAC activity were lower in IL-13–exposed ASM, but calcitriol enhanced HDAC expression/activity.>Conclusions: In asthmatic ASM, Vit D functionality is maintained, allowing calcitriol to reduce the procontractile and proremodeling effects of inflammatory cytokines, particularly IL-13, which is relevant to asthma. These findings highlight a potential role for Vit D in asthma pathogenesis, particularly in the context of airway structure and functional changes early in disease.
机译:>背景:尽管多项临床研究发现维生素D(Vit D)缺乏与哮喘之间存在关联,但最近的一项临床研究表明,补充Vit D缺乏治疗效果。然而,在炎症和哮喘的情况下,Vit D影响气道结构和功能的机制仍未确定。在这方面,鉴于这种细胞类型在过度收缩和重塑中的作用,Vit D对气道平滑肌(ASM)的作用很重要。我们评估了Vit D调节促炎细胞因子肿瘤坏死因子-α(TNF-α)和IL-13对细胞内Ca 2 + ([Ca 2+ < / sup>] i)在非哮喘和哮喘人ASM中的水平和重塑。>方法:从临床上定义为轻度至中度哮喘与非哮喘患者的手术肺标本中酶分离人ASM。在存在或不存在100 nM骨化三醇的情况下,用10 ng / mlTNF-α和50 ng / ml IL-13处理细胞。>测量和主要结果:有趣的是,Vit D受体(VDR)和接受TNF-α和IL-13治疗的哮喘患者,其维甲酸X受体-α水平得以维持,甚至升高。与未处理的细胞相比,骨化三醇减弱了TNF-α对ASM中对组胺的[Ca 2 + ] i反应的增强作用。骨化三醇尤其使TNF-α和IL-13对胶原和纤连蛋白沉积的影响减弱,尤其是在哮喘性ASM中。骨化三醇甚至在患有哮喘和患有IL-13的受试者中也能刺激VDR /视黄酸X受体二聚化和VDR活性,突出了保留的功能。在暴露于IL-13的ASM中,I类组蛋白脱乙酰基酶1-3(HDAC)的表达和总体HDAC活性较低,但骨化三醇增强了HDAC的表达/活性。>结论:在哮喘ASM中,Vit D功能维持钙离子维持,可使骨化三醇减少与哮喘有关的炎性细胞因子,特别是IL-13的收缩和重塑作用。这些发现突出了Vit D在哮喘发病机理中的潜在作用,特别是在疾病早期的气道结构和功能改变的背景下。

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