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核仁素作为MRL/lpr狼疮易感小鼠产生的自身抗体的最早靶分子。

Nucleolin as the earliest target molecule of autoantibodies produced in MRL/lpr lupus-prone mice.

作者信息

Hirata D, Iwamoto M, Yoshio T, Okazaki H, Masuyama J, Mimori A, Minota S

机构信息

Division of Rheumatology and Clinical Immunology, Jichi Medical School, Minamikawachi-Machi, Tochigi, 329-0498, Japan.

出版信息

Clin Immunol. 2000 Oct;97(1):50-8. doi: 10.1006/clim.2000.4916.

Abstract

To elucidate the autoantigen against which autoantibodies are produced in the earliest phase of the disease process of systemic lupus erythematosus (SLE), serum samples were collected individually and serially from 10 NZB/NZW F1 and 10 MRL/lpr mice. Using immunoblots with mouse thymoma cell (EL-4) lysates as substrates, all mice were found to generate autoantibody against an either 150-kDa, 110-kDa, 75-kDa, or 55-kDa molecule in as early as 4 weeks. Anti-DNA antibodies occurred almost at the same time or after those against these four molecules. The number of antigens reactive with autoantibodies in immunoblots increased gradually with age. Antibodies against histone molecules were produced after 8 weeks of age. Among the four antigens, the 110-kDa molecule was identified as nucleolin, which is an abundant nucleolar phosphoprotein. Nucleolin binds DNA, RNA, and nucleic acid-binding proteins such as histone H1. Nucleolin is a target of granzyme A of cytotoxic T cells, and autoantibodies against it are found in sera from patients with SLE as well as from those with various viral infections. These results indicate that nucleolin is one of the immunodominant molecules that break down self-tolerance and initiate autoantibody-spreading in a mouse model of SLE.

摘要

为了阐明在系统性红斑狼疮(SLE)疾病进程的最早阶段产生自身抗体所针对的自身抗原,分别连续收集了10只NZB/NZW F1小鼠和10只MRL/lpr小鼠的血清样本。以小鼠胸腺瘤细胞(EL-4)裂解物为底物进行免疫印迹分析,发现所有小鼠早在4周龄时就产生了针对150 kDa、110 kDa、75 kDa或55 kDa分子的自身抗体。抗DNA抗体几乎在针对这四种分子的自身抗体出现的同时或之后出现。免疫印迹中与自身抗体反应的抗原数量随年龄逐渐增加。8周龄后产生了针对组蛋白分子的抗体。在这四种抗原中,110 kDa分子被鉴定为核仁素,它是一种丰富的核仁磷蛋白。核仁素结合DNA、RNA以及诸如组蛋白H1等核酸结合蛋白。核仁素是细胞毒性T细胞颗粒酶A的靶标,在SLE患者以及各种病毒感染患者的血清中都发现了针对它的自身抗体。这些结果表明,核仁素是在SLE小鼠模型中打破自身耐受性并引发自身抗体扩散的免疫显性分子之一。

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