MECHANISMS REGULATING NEUROMUSCULAR JUNCTION DEVELOPMENT AND FUNCTION AND CAUSES OF MUSCLE WASTING

被引:313
作者
Tintignac, Lionel A.
Brenner, Hans-Rudolf
Rueegg, Markus A. [1 ]
机构
[1] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
NICOTINIC ACETYLCHOLINE-RECEPTOR; CONGENITAL MYASTHENIC SYNDROME; EXTENDS LIFE-SPAN; DYSTROPHIN-ASSOCIATED GLYCOPROTEINS; UBIQUITIN-PROTEASOME SYSTEM; POSTSYNAPTIC-LIKE APPARATUS; TERMINAL SCHWANN-CELLS; GATED SODIUM-CHANNELS; MOTOR AXON OUTGROWTH; TYROSINE KINASE MUSK;
D O I
10.1152/physrev.00033.2014
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The neuromuscular junction is the chemical synapse between motor neurons and skeletal muscle fibers. It is designed to reliably convert the action potential from the presynaptic motor neuron into the contraction of the postsynaptic muscle fiber. Diseases that affect the neuromuscular junction may cause failure of this conversion and result in loss of ambulation and respiration. The loss of motor input also causes muscle wasting as muscle mass is constantly adapted to contractile needs by the balancing of protein synthesis and protein degradation. Finally, neuromuscular activity and muscle mass have a major impact on metabolic properties of the organisms. This review discusses the mechanisms involved in the development and maintenance of the neuromuscular junction, the consequences of and the mechanisms involved in its dysfunction, and its role in maintaining muscle mass during aging. As life expectancy is increasing, loss of muscle mass during aging, called sarcopenia, has emerged as a field of high medical need. Interestingly, aging is also accompanied by structural changes at the neuromuscular junction, suggesting that the mechanisms involved in neuromuscular junction maintenance might be disturbed during aging. In addition, there is now evidence that behavioral paradigms and signaling pathways that are involved in longevity also affect neuromuscular junction stability and sarcopenia.
引用
收藏
页码:809 / 852
页数:44
相关论文
共 492 条
[1]   Congenital Myasthenic Syndromes: Achievements and Limitations of Phenotype-Guided Gene-After-Gene Sequencing in Diagnostic Practice: A Study of 680 Patients [J].
Abicht, Angela ;
Dusl, Marina ;
Gallenmueller, Constanze ;
Guergueltcheva, Velina ;
Schara, Ulrike ;
Della Marina, Adele ;
Wibbeler, Eva ;
Almaras, Sybille ;
Mihaylova, Violeta ;
von der Hagen, Maja ;
Huebner, Angela ;
Chaouch, Amina ;
Mueller, Juliane S. ;
Lochmueller, Hanns .
HUMAN MUTATION, 2012, 33 (10) :1474-1484
[2]   Rapid and reversible effects of activity on acetylcholine receptor density at the neuromuscular junction in vivo [J].
Akaaboune, M ;
Culican, SM ;
Turney, SG ;
Lichtman, JW .
SCIENCE, 1999, 286 (5439) :503-507
[3]  
Allan DW, 1997, J COMP NEUROL, V382, P469, DOI 10.1002/(SICI)1096-9861(19970616)382:4<469::AID-CNE4>3.0.CO
[4]  
2-0
[5]  
Allan DW, 1997, J COMP NEUROL, V382, P459, DOI 10.1002/(SICI)1096-9861(19970616)382:4<459::AID-CNE3>3.0.CO
[6]  
2-1
[7]   Activation of serum/glucocorticoid-induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy [J].
Andres-Mateos, Eva ;
Brinkmeier, Heinrich ;
Burks, Tyesha N. ;
Mejias, Rebeca ;
Files, Daniel C. ;
Steinberger, Martin ;
Soleimani, Arshia ;
Marx, Ruth ;
Simmers, Jessica L. ;
Lin, Benjamin ;
Hedderick, Erika Finanger ;
Marr, Tom G. ;
Lin, Brian M. ;
Hourde, Christophe ;
Leinwand, Leslie A. ;
Kuhl, Dietmar ;
Foeller, Michael ;
Vogelsang, Silke ;
Hernandez-Diaz, Ivan ;
Vaughan, Dana K. ;
Alvarez de la Rosa, Diego ;
Lang, Florian ;
Cohn, Ronald D. .
EMBO MOLECULAR MEDICINE, 2013, 5 (01) :80-91
[8]  
[Anonymous], J NEUROSCI IN PRESS
[9]  
[Anonymous], AUTOPHAGY
[10]   β Integrin Tyrosine Phosphorylation Is a Conserved Mechanism for Regulating Talin-induced Integrin Activation [J].
Anthis, Nicholas J. ;
Haling, Jacob R. ;
Oxley, Camilla L. ;
Memo, Massimiliano ;
Wegener, Kate L. ;
Lim, Chinten J. ;
Ginsberg, Mark H. ;
Campbell, Iain D. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (52) :36700-36710