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首页> 外文期刊>OMICS: A journal of integrative biology >The Nutrigenomics of Asthma: Molecular Mechanisms of Airway Neutrophilia following Dietary Antioxidant Withdrawal
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The Nutrigenomics of Asthma: Molecular Mechanisms of Airway Neutrophilia following Dietary Antioxidant Withdrawal

机译:哮喘的营养基因组学:分子机制饮食后的气道嗜中性抗氧化剂撤军

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Depletion of antioxidants through consumption of a low antioxidant diet has been reported to increase neutrophilic airway inflammation and worsen symptoms of asthma. Using a nutrigenomics approach, this study explores the mechanisms of airway neutrophilic inflammation due to depletion of dietary antioxidants. Induced sputum samples were collected at baseline and after participants consumed a low antioxidant diet for 14 days. Genome-wide gene expression profiles were generated from sputum RNA samples from participants with a >10% change in sputum neutrophils using Illumina Humanref-8 expression microarrays. There were 104 genes differentially expressed following the dietary change. Upregulated genes were involved in the innate immune response and included the innate immune receptors TLR2, IL1R2, CD93, the signaling molecules IRAK2, IRAK3, and neutrophil proteases MMP25 and CPD. Downregulated genes included those involved in endogenous antioxidant defenses (GSTA1, GSTA2) and protease inhibition (SLPI, SERPINB3). Altered expression of five genes (TLR2, IRAK2, IL1R2, C20orf114, and SERPINB3) was confirmed using real-time polymerase chain reaction (PCR). These observations suggest that depletion of dietary antioxidants in asthma may result in upregulation of genes involved in the innate immune response. A diet low in antioxidants may be contributing to the development of neutrophilic asthma through activation of the innate immune response.
机译:通过消费的损耗的抗氧化剂低抗氧化剂饮食已被报道中性气道炎症和增加恶化哮喘的症状。的方法,本研究探讨了机制由于损耗气道中性粒细胞炎症的膳食抗氧化剂。在基线和后参与者收集吗消耗低抗氧化剂饮食为14天。全基因组基因表达谱从痰液生成RNA样本参与者痰> 10%变化中性粒细胞使用Illumina公司Humanref-8表达式微阵列。表达后的饮食变化。调节基因参与了天生的免疫反应,包括先天免疫受体TLR2、IL1R2 CD93信号分子IRAK2、IRAK3和中性白细胞蛋白酶MMP25 CPD。参与内源性抗氧化防御(GSTA1 GSTA2)和蛋白酶抑制(SLPI,SERPINB3)。(IL1R2 TLR2 IRAK2 C20orf114, SERPINB3)使用实时聚合酶链证实反应(PCR)。损耗的膳食抗氧化剂在哮喘可能导致upregulation基因参与先天免疫反应。抗氧化剂可能导致中性粒细胞哮喘的发展激活先天免疫应答的。

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