Sympathetic innervation in skeletal muscle and its role at the neuromuscular junction

IF 1.8 3区 生物学 Q4 CELL BIOLOGY Journal of Muscle Research and Cell Motility Pub Date : 2024-02-17 DOI:10.1007/s10974-024-09665-9
Rüdiger Rudolf, Isis C. Kettelhut, Luiz Carlos C. Navegantes
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Abstract

Neuromuscular junctions are the synapses between motor neurons and skeletal muscle fibers, which mediate voluntary muscle movement. Since neuromuscular junctions are also tightly associated with the capping function of terminal Schwann cells, these synapses have been classically regarded as tripartite chemical synapses. Although evidences from sympathetic innervation of neuromuscular junctions was described approximately a century ago, the essential presence and functional relevance of sympathetic contribution to the maintenance and modulation of neuromuscular junctions was demonstrated only recently. These findings shed light on the pathophysiology of different clinical conditions and can optimize surgical and clinical treatment modalities for skeletal muscle disorders.

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骨骼肌中的交感神经支配及其在神经肌肉接头处的作用
神经肌肉接头是运动神经元与骨骼肌纤维之间的突触,是肌肉自主运动的媒介。由于神经肌肉接头也与末端许旺细胞的封盖功能密切相关,这些突触一直被视为三方化学突触。虽然约一个世纪前就有交感神经支配神经肌肉接头的证据,但交感神经对维持和调节神经肌肉接头的重要作用和功能相关性直到最近才得到证实。这些发现揭示了不同临床病症的病理生理学,可优化骨骼肌疾病的手术和临床治疗方法。
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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
21
审稿时长
>12 weeks
期刊介绍: The Journal of Muscle Research and Cell Motility has as its main aim the publication of original research which bears on either the excitation and contraction of muscle, the analysis of any one of the processes involved therein, the processes underlying contractility and motility of animal and plant cells, the toxicology and pharmacology related to contractility, or the formation, dynamics and turnover of contractile structures in muscle and non-muscle cells. Studies describing the impact of pathogenic mutations in genes encoding components of contractile structures in humans or animals are welcome, provided they offer mechanistic insight into the disease process or the underlying gene function. The policy of the Journal is to encourage any form of novel practical study whatever its specialist interest, as long as it falls within this broad field. Theoretical essays are welcome provided that they are concise and suggest practical ways in which they may be tested. Manuscripts reporting new mutations in known disease genes without validation and mechanistic insight will not be considered. It is the policy of the journal that cells lines, hybridomas and DNA clones should be made available by the developers to any qualified investigator. Submission of a manuscript for publication constitutes an agreement of the authors to abide by this principle.
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