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Detection of loci for allergic asthma using SMXA recombinant inbred strains of mice

机译:使用SMXA重组自交系小鼠检测过敏性哮喘的基因座

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摘要

Asthma is regarded as a multifactorial inflammatory disorder arising as a result of inappropriate immune responses in genetically susceptible individuals to common environmental antigens. However, the precise molecular basis is unknown. To identify genes for susceptibility to three asthma-related traits, airway hyperresponsiveness (AHR), eosinophil infiltration, and allergen-specific serum IgE levels, we conducted a genetic analysis using SMXA recombinant inbred (RI) strains of mice. Quantitative trait locus analysis detected a significant locus for AHR on chromosome 17. For eosinophil infiltration, significant loci were detected on chromosomes 9 and 16. Although we could not detect any significant loci for allergen-specific serum IgE, analysis of consomic strains showed that chromosomes 17 and 19 carried genes that affected this trait. We detected genetic susceptibility loci that separately regulated the three asthma-related phenotypes. Our results suggested that different genetic mechanisms regulate these asthma-related phenotypes. Genetic analyses using murine RI and consomic strains enhance understanding of the molecular mechanisms of asthma in human.
机译:哮喘被视为多因素性炎症,是遗传易感人群对常见环境抗原的不适当免疫反应导致的。但是,确切的分子基础尚不清楚。为了确定对三种哮喘相关性状,气道高反应性(AHR),嗜酸性粒细胞浸润和变应原特异性血清IgE水平易感性的基因,我们使用小鼠SMXA重组自交系(RI)进行了遗传分析。数量性状基因座分析在17号染色​​体上检测到AHR的重要基因座。对于嗜酸性粒细胞浸润,在9号和16号染色体上检测到了重要基因座。尽管我们无法检测到任何过敏原特异性血清IgE的重要基因座,但对纯菌株的分析表明,染色体17和19携带了影响该性状的基因。我们检测到遗传易感性基因座,分别调节了三种与哮喘相关的表型。我们的结果表明,不同的遗传机制调控这些与哮喘相关的表型。使用鼠类RI和清毒菌株进行的遗传分析可增强对人类哮喘分子机制的了解。

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