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将Ncf1定位为调控大鼠关节炎严重程度的基因。

Positional identification of Ncf1 as a gene that regulates arthritis severity in rats.

作者信息

Olofsson Peter, Holmberg Jens, Tordsson Jesper, Lu Shemin, Akerström Bo, Holmdahl Rikard

机构信息

Section for Medical Inflammation Research and Department of Cell and Molecular Biology, Sölvegatan 19, I11 BMC, Lund University, S-22184 Lund, Sweden.

出版信息

Nat Genet. 2003 Jan;33(1):25-32. doi: 10.1038/ng1058. Epub 2002 Dec 2.

Abstract

The identification of genes underlying quantitative-trait loci (QTL) for complex diseases, such as rheumatoid arthritis, is a challenging and difficult task for the human genome project. Through positional cloning of the Pia4 QTL in rats, we found that a naturally occurring polymorphism of Ncf1 (encoding neutrophil cytosolic factor 1, a component of the NADPH oxidase complex) regulates arthritis severity. The disease-related allele of Ncf1 has reduced oxidative burst response and promotes activation of arthritogenic T cells. Pharmacological treatment with substances that activate the NADPH oxidase complex is shown to ameliorate arthritis. Hence, Ncf1 is associated with a new autoimmune mechanism leading to severe destructive arthritis, notably similar to rheumatoid arthritis in humans.

摘要

对于人类基因组计划而言,鉴定类风湿关节炎等复杂疾病的数量性状基因座(QTL)相关基因是一项具有挑战性的艰巨任务。通过对大鼠中Pia4 QTL进行定位克隆,我们发现Ncf1(编码中性粒细胞胞质因子1,一种NADPH氧化酶复合物的组成成分)的自然多态性调节关节炎的严重程度。Ncf1与疾病相关的等位基因具有降低的氧化爆发反应,并促进致关节炎T细胞的激活。已证明用激活NADPH氧化酶复合物的物质进行药物治疗可改善关节炎。因此,Ncf1与一种导致严重破坏性关节炎的新自身免疫机制相关,这种机制与人类类风湿关节炎显著相似。

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