Building, Breaking, and Repairing Neuromuscular Synapses

IF 6.9 2区 生物学 Q1 CELL BIOLOGY
Ruth Herbst, Maartje G. Huijbers, Julien Oury, Steven J. Burden
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引用次数: 0

Abstract

A coordinated and complex interplay of signals between motor neurons, skeletal muscle cells, and Schwann cells controls the formation and maintenance of neuromuscular synapses. Deficits in the signaling pathway for building synapses, caused by mutations in critical genes or autoantibodies against key proteins, are responsible for several neuromuscular diseases, which cause muscle weakness and fatigue. Here, we describe the role that four key genes, Agrin, Lrp4, MuSK, and Dok7, play in this signaling pathway, how an understanding of their mechanisms of action has led to an understanding of several neuromuscular diseases, and how this knowledge has contributed to emerging therapies for treating neuromuscular diseases.
神经肌肉突触的建立、破坏和修复
运动神经元、骨骼肌细胞和许旺细胞之间协调而复杂的信号相互作用,控制着神经肌肉突触的形成和维持。关键基因突变或针对关键蛋白的自身抗体导致突触形成信号通路的缺陷,是导致肌无力和疲劳的多种神经肌肉疾病的原因。在此,我们将介绍 Agrin、Lrp4、MuSK 和 Dok7 这四个关键基因在这一信号通路中的作用,了解这些基因的作用机制如何有助于我们了解几种神经肌肉疾病,以及这些知识如何有助于开发治疗神经肌肉疾病的新疗法。
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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来源期刊
CiteScore
15.00
自引率
1.40%
发文量
56
审稿时长
3-8 weeks
期刊介绍: Cold Spring Harbor Perspectives in Biology offers a comprehensive platform in the molecular life sciences, featuring reviews that span molecular, cell, and developmental biology, genetics, neuroscience, immunology, cancer biology, and molecular pathology. This online publication provides in-depth insights into various topics, making it a valuable resource for those engaged in diverse aspects of biological research.
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