Molecular mechanisms underlying maturation and maintenance of the vertebrate neuromuscular junction

被引:113
|
作者
Shi, Lei [1 ,2 ,3 ]
Fu, Amy K. Y. [1 ,2 ,3 ]
Ip, Nancy Y. [1 ,2 ,3 ]
机构
[1] Hong Kong Univ Sci & Technol, Div Life Sci, Hong Kong, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, State Key Lab Mol Neurosci, Hong Kong, Hong Kong, Peoples R China
[3] Jinan Univ, JNU HKUST Joint Lab Neurosci & Innovat Drug Res, Guangzhou 510632, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
synapse; acetylcholine receptor; neuromuscular disorder; congenital myasthenic syndrome; agrin; MuSK; NICOTINIC ACETYLCHOLINE-RECEPTOR; CONGENITAL MYASTHENIC SYNDROME; DYSTROPHIN-GLYCOPROTEIN COMPLEX; SPINAL MUSCULAR-ATROPHY; UTROPHIN-DEFICIENT MICE; CELL-ADHESION MOLECULE; MOTOR-NERVE TERMINALS; TYROSINE KINASE MUSK; SYNAPSE FORMATION; IN-VIVO;
D O I
10.1016/j.tins.2012.04.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The vertebrate neuromuscular junction (NMJ), a peripheral synapse formed between motoneuron and skeletal muscle, is characterized by a protracted postnatal period of maturation and life-long maintenance. In neuromuscular disorders such as congenital myasthenic syndromes (CMSs), disruptions of NMJ maturation and/or maintenance are frequently observed. In particular, defective neuromuscular transmission associated with structural and molecular abnormalities at the pre- and postsynaptic membranes, as well as at the synaptic cleft, has been reported in these patients. Here, we review recent advances in the understanding of molecular and cellular events that mediate NMJ maturation and maintenance. The underlying regulatory mechanisms, including key molecular regulators at the presynaptic nerve terminal, synaptic cleft, and postsynaptic muscle membrane, are discussed.
引用
收藏
页码:441 / 453
页数:13
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