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肌萎缩侧索硬化症及其他神经退行性疾病中的蛋白质瓜氨酸化

Protein Citrullination in Amyotrophic Lateral Sclerosis and Other Neurodegenerative Diseases.

作者信息

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

机构信息

Department of Biochemistry and Molecular Biotechnology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.

Program in Chemical Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605 USA.

出版信息

J Exp Neurol. 2024;5(4):183-191. doi: 10.33696/neurol.5.101.

Abstract

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.

摘要

蛋白质瓜氨酸化(PC)是一种翻译后修饰(PTM),它将肽基精氨酸转化为肽基瓜氨酸。异常的PC是神经退行性疾病的一个标志,包括肌萎缩侧索硬化症(ALS)、阿尔茨海默病、帕金森病、朊病毒病和多发性硬化症。这些疾病的共同特征是反应性星形胶质细胞中PC显著增加。一些瓜氨酸化蛋白已被鉴定出来。最突出的是星形胶质细胞骨架蛋白,如胶质纤维酸性蛋白(GFAP)和波形蛋白,以及髓鞘蛋白髓鞘碱性蛋白(MBP)。最近对ALS的研究揭示了新的变化,包括神经元中PC减少以及PC与髓鞘蛋白聚集体的关联。这些发现表明,PC促成了蛋白质聚集、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。需要进一步研究来理解一系列问题,从PC如何调节单个蛋白质功能到其对疾病的影响。由于PC在神经退行性疾病中发生显著变化,这种PTM也有可能被用作生物标志物,并且调节这种PTM可能是一种治疗途径。在这篇综述中,我们总结了目前对ALS和其他神经退行性疾病中PC的理解、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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