Cell models for studying myasthenia gravis.

International review of neurobiology Pub Date : 2025-01-01 Epub Date: 2025-06-23 DOI:10.1016/bs.irn.2025.04.026
Yu-Fang Huang, Robyn L K Verpalen, Anna Rostedt Punga, Maartje G Huijbers
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Abstract

Understanding the pathophysiology of Myasthenia Gravis (MG) and developing effective treatments requires using cell models that replicate key features of the disease, particularly those involved in the autoimmune response and neuromuscular dysfunction. This chapter reviews the various cell-based models used in MG research and those with potential for preclinical MG studies, including muscle cells and co-culture models to form neuromuscular junctions (NMJ). We discuss the strengths and limitations of these models, further outline methods for characterizing these, and provide an outlook on the future refinement and abilities of cell models for advancing MG research.

研究重症肌无力的细胞模型。
了解重症肌无力(MG)的病理生理学和开发有效的治疗方法需要使用复制该疾病关键特征的细胞模型,特别是那些涉及自身免疫反应和神经肌肉功能障碍的细胞模型。本章回顾了肌萎缩症研究中使用的各种基于细胞的模型,以及那些具有临床前肌萎缩症研究潜力的模型,包括肌肉细胞和形成神经肌肉连接(NMJ)的共培养模型。我们讨论了这些模型的优势和局限性,进一步概述了表征这些模型的方法,并展望了未来细胞模型的改进和能力,以推进MG研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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