肌萎缩性侧索硬化症和其他神经退行性疾病的瓜氨酸化蛋白。

Issa O Yusuf, Webb Camille, Paul R Thompson, Zuoshang Xu
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摘要

蛋白瓜氨酸化是将肽基精氨酸转化为肽基瓜氨酸的翻译后修饰(PTM)。异常PC是神经退行性疾病的标志,包括肌萎缩性侧索硬化症(ALS)、阿尔茨海默病、帕金森病、朊病毒病和多发性硬化症。在这些疾病中常见的是反应性星形胶质细胞中PC的急剧增加。已经鉴定出一些瓜氨酸化蛋白。最突出的是星形细胞骨架蛋白,如GFAP和vimentin,以及髓磷脂蛋白MBP。最近对ALS的研究揭示了新的变化,包括神经元中PC的减少和PC与髓鞘蛋白聚集的关联。这些发现表明,PC有助于蛋白质聚集、神经元功能障碍、神经炎症和轴突变性。然而,PC如何影响神经退行性变仍有待了解。需要进一步的研究来了解一系列问题,从PC如何调节个体蛋白质功能到其对疾病的影响。由于PTM在神经退行性疾病中的强大变化,PTM也有可能被利用为生物标志物,并且调节PTM可能是治疗的途径。在这篇综述中,我们总结了目前对肌萎缩侧索硬化症和其他神经退行性疾病中PC的认识,PC的研究方法,以及PC作为生物标志物和治疗靶点的潜力。
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Protein Citrullination in Amyotrophic Lateral Sclerosis and Other Neurodegenerative Diseases.

Protein citrullination (PC) is a posttranslational modification (PTM) that converts a peptidyl arginine into a peptidyl citrulline. Aberrant PC is a hallmark of neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS), Alzheimer's disease, Parkinson's disease, prion disease, and multiple sclerosis. Common among these diseases is a dramatic increase of PC in reactive astrocytes. Some citrullinated proteins have been identified. The most prominent are astrocytic cytoskeletal proteins such as GFAP and vimentin, and myelin protein MBP. Recent investigation in ALS has revealed new changes, including a decreased PC in neurons and an association of PC with myelin protein aggregates. These findings suggest that PC contributes to protein aggregation, neuronal dysfunction, neuroinflammation, and axonal degeneration. However, how PC impact neurodegeneration remains to be understood. Further studies are needed to understand a range of questions, from how PC modulates individual protein functions to its impact on diseases. Because of the PC's robust changes in neurodegenerative diseases, there are also prospects that this PTM may be harnessed as biomarkers, and modulation of this PTM may be an avenue for therapy. In this review, we summarize the current understanding of PC in ALS and other neurodegenerative diseases, the investigative methods for PC, and PC's potential as a biomarker and a therapeutic target.

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