Targeting neuromuscular junction to treat neuromuscular disorders

被引:8
|
作者
Qaisar, Rizwan [1 ,2 ,3 ,4 ]
机构
[1] Univ Sharjah, Coll Med, Basic Med Sci, Sharjah, U Arab Emirates
[2] Univ Sharjah, Sharjah Inst Med & Hlth Sci, Space Med Res Grp, Sharjah 27272, U Arab Emirates
[3] Univ Sharjah, Sharjah Inst Med & Hlth Sci, Cardiovasc Res Grp, Sharjah 27272, U Arab Emirates
[4] Univ Sharjah, Coll Med, Dept Basic Med Sci, Sharjah, U Arab Emirates
关键词
Neuromuscular junction; Chronic obstructive pulmonary disease; Muscle wasting; CONGENITAL MYASTHENIC SYNDROME; GENE-THERAPY; REGULATES MATURATION; MUSCLE; AGRIN; MUSK; PHOSPHORYLATION; MUTATIONS; IMPROVES; PROTEIN;
D O I
10.1016/j.lfs.2023.122186
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The integrity and preservation of the neuromuscular junction (NMJ), the interface between the motor neuron and skeletal muscle, is critical for maintaining a healthy skeletal muscle. The structural and/or functional defects in the three cellular components of NMJ, namely the pre-synaptic terminal, synaptic cleft, and post-synaptic region, negatively affect skeletal muscle mass and/or strength. Therefore, NMJ repair appears to be an appropriate therapy for muscle disorders. Mouse models provide a detailed molecular characterization of various cellular components of NMJ with relevance to human diseases. This review discusses different molecular targets on the three cellular components of NMJ for treating muscle diseases. The potential effects of these therapies on NMJ morphology and motor performance, their therapeutic efficacy, and clinical relevance are discussed. Collectively, the available data supports targeting NMJ alone or as an adjunct therapy in treating muscle disorders. However, the potential impact of such interventions on human patients with muscle disorders requires further investigation.
引用
收藏
页数:10
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