Muscle type and fiber type specificity in muscle wasting

被引:473
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
相关论文
共 88 条
[21]   Loss of myostatin expression alters fiber-type distribution and expression of myosin heavy chain isoforms in slow- and fast-type skeletal muscle [J].
Girgenrath, S ;
Song, K ;
Whittemore, LA .
MUSCLE & NERVE, 2005, 31 (01) :34-40
[22]   RELATIONSHIP BETWEEN CORTISONE AND MUSCLE WORK IN DETERMINING MUSCLE SIZE [J].
GOLDBERG, AL ;
GOODMAN, HM .
JOURNAL OF PHYSIOLOGY-LONDON, 1969, 200 (03) :667-&
[23]   Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy [J].
Gomes, MD ;
Lecker, SH ;
Jagoe, RT ;
Navon, A ;
Goldberg, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) :14440-14445
[24]  
GRIMBY G, 1976, SCAND J REHABIL MED, V8, P37
[25]  
Hasselgren P O, 1999, Curr Opin Clin Nutr Metab Care, V2, P201, DOI 10.1097/00075197-199905000-00002
[26]   Genetic Deletion of Myostatin From the Heart Prevents Skeletal Muscle Atrophy in Heart Failure [J].
Heineke, Joerg ;
Auger-Messier, Mannix ;
Xu, Jian ;
Sargent, Michelle ;
York, Allen ;
Welle, Stephen ;
Molkentin, Jeffery D. .
CIRCULATION, 2010, 121 (03) :419-425
[27]  
HERBISON GJ, 1979, ARCH PHYS MED REHAB, V60, P401
[28]   SKELETAL-MUSCLE ATROPHY IN OLD RATS - DIFFERENTIAL CHANGES IN THE 3 FIBER TYPES [J].
HOLLOSZY, JO ;
CHEN, M ;
CARTEE, GD ;
YOUNG, JC .
MECHANISMS OF AGEING AND DEVELOPMENT, 1991, 60 (02) :199-213
[29]   Endogenous glucocorticoids and impaired insulin signaling are both required to stimulate muscle wasting under pathophysiological conditions in mice [J].
Hu, Zhaoyong ;
Wang, Huiling ;
Lee, In Hee ;
Du, Jie ;
Mitch, William E. .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (10) :3059-3069
[30]   'Fast' and 'slow' muscle fibres in hindlimb muscles of adult rats regenerate from intrinsically different satellite cells [J].
Kalhovde, JM ;
Jerkovic, R ;
Sefland, I ;
Cordonnier, C ;
Calabria, E ;
Schiaffino, S ;
Lomo, T .
JOURNAL OF PHYSIOLOGY-LONDON, 2005, 562 (03) :847-857