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自身免疫与免疫介导性神经疾病中神经退行性变之间的潜在联系。

A potential link between autoimmunity and neurodegeneration in immune-mediated neurological disease.

机构信息

Veterans Administration Medical Center, 1030 Jefferson Avenue, Memphis, TN 38104, USA.

出版信息

J Neuroimmunol. 2011 Jun;235(1-2):56-69. doi: 10.1016/j.jneuroim.2011.02.007. Epub 2011 May 13.

Abstract

Multiple sclerosis (MS) patients make antibodies to heterogeneous nuclear ribonuclear protein A1 (hnRNP-A1), a nucleocytoplasmic protein. We hypothesized this autoimmune reaction might contribute to neurodegeneration. Antibodies from MS patients reacted with hnRNP-A1-'M9', its nuclear translocation sequence. Transfection of anti-M9 antibodies into neurons resulted in neuronal injury and changes in transcripts related to hnRNP-A1 function. Importantly, RNA levels for the spinal paraplegia genes (SPGs) decreased. Changes in SPG RNA levels were confirmed in neurons purified from MS brains. Also, we show molecular interactions between spastin (the encoded protein of SPG4) and hnRNP-A1. These data suggest a link between autoimmunity, clinical phenotype and neurodegeneration in MS.

摘要

多发性硬化症 (MS) 患者会产生针对核浆蛋白异质核核糖核蛋白 A1 (hnRNP-A1) 的抗体。我们假设这种自身免疫反应可能导致神经退行性变。来自 MS 患者的抗体与 hnRNP-A1 的核转位序列“M9”反应。将抗-M9 抗体转染到神经元中会导致神经元损伤和与 hnRNP-A1 功能相关的转录本发生变化。重要的是,与脊髓性肌萎缩症基因(SPG)相关的 RNA 水平降低。从 MS 大脑中纯化的神经元中证实了 SPG RNA 水平的变化。此外,我们还展示了痉挛蛋白(SPG4 编码蛋白)和 hnRNP-A1 之间的分子相互作用。这些数据表明自身免疫、临床表型和 MS 中的神经退行性变之间存在联系。

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