Muscle type and fiber type specificity in muscle wasting

被引:466
作者
Ciciliot, Stefano [1 ]
Rossi, Alberto C. [1 ]
Dyar, Kenneth A. [1 ]
Blaauw, Bert [1 ,2 ]
Schiaffino, Stefano [1 ,3 ]
机构
[1] VIMM, I-35129 Padua, Italy
[2] Univ Padua, Dept Biomed Sci, Padua, Italy
[3] CNR, Inst Neurosci, Padua, Italy
关键词
Muscle atrophy; Muscle fiber types; Cachexia; Muscular dystrophies; Muscle disuse; Sarcopenia; MYOSIN HEAVY-CHAIN; HUMAN SKELETAL-MUSCLE; FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY; OBSTRUCTIVE PULMONARY-DISEASE; FOXO TRANSCRIPTION FACTORS; RAT SOLEUS MUSCLE; FAST-TWITCH; UBIQUITIN LIGASES; HEART-FAILURE; IN-VIVO;
D O I
10.1016/j.biocel.2013.05.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Muscle wasting occurs in a variety of conditions, including both genetic diseases, such as muscular dystrophies, and acquired disorders, ranging from muscle disuse to cancer cachexia, from heart failure to aging sarcopenia. In most of these conditions, the loss of muscle tissue is not homogeneous, but involves specific muscle groups, for example Duchenne muscular dystrophy affects most body muscles but spares extraocular muscles, and other dystrophies affect selectively proximal or distal limb muscles. In addition, muscle atrophy can affect specific fiber types, involving predominantly slow type 1 or fast type 2 muscle fibers, and is frequently accompanied by a slow-to-fast or fast-to-slow fiber type shift. For example, muscle disuse, such as spinal cud injury, causes type 1 fiber atrophy with a slow-to-fast fiber type shift, whereas cancer cachexia leads to preferential atrophy of type 2 fibers with a fast-to-slow fiber type shift. The identification of the signaling pathways responsible for the differential response of muscles types and filer types can lead to a better understanding of the pathogenesis of muscle wasting and to the design of therapeutic interventions appropriate for the specific disorders. This article is part of a Directed Issue entitled: Molecular basis of muscle wasting. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2191 / 2199
页数:9
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