Muscle Satellite Cells: Exploring the Basic Biology to Rule Them

被引:41
作者
Almeida, Camila F. [1 ]
Fernandes, Stephanie A. [1 ]
Ribeiro Junior, Antonio F. [1 ]
Okamoto, Oswaldo Keith [1 ]
Vainzof, Mariz [1 ]
机构
[1] IBUSP, Human Genome & Stem Cell Res Ctr, Rua Matao 106,Cidade Univ, BR-5508900 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
HUMAN SKELETAL-MUSCLE; DUCHENNE MUSCULAR-DYSTROPHY; HEMATOPOIETIC STEM-CELLS; TEMPLATE DNA STRANDS; ADULT BONE-MARROW; SELF-RENEWAL; MOLECULAR REGULATION; FIBRO/ADIPOGENIC PROGENITORS; MYOBLAST TRANSPLANTATION; REVERSIBLE QUIESCENCE;
D O I
10.1155/2016/1078686
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Adult skeletal muscle is a postmitotic tissue with an enormous capacity to regenerate upon injury. This is accomplished by resident stem cells, named satellite cells, which were identified more than 50 years ago. Since their discovery, many researchers have been concentrating efforts to answer questions about their origin and role in muscle development, the way they contribute to muscle regeneration, and their potential to cell-based therapies. Satellite cells are maintained in a quiescent state and upon requirement are activated, proliferating, and fusing with other cells to form or repair myofibers. In addition, they are able to self-renew and replenish the stem pool. Every phase of satellite cell activity is highly regulated and orchestrated by many molecules and signaling pathways; the elucidation of players and mechanisms involved in satellite cell biology is of extreme importance, being the first step to expose the crucial points that could be modulated to extract the optimal response from these cells in therapeutic strategies. Here, we review the basic aspects about satellite cells biology and briefly discuss recent findings about therapeutic attempts, trying to raise questions about how basic biology could provide a solid scaffold to more successful use of these cells in clinics.
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页数:14
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共 176 条
[1]
ALLBROOK DB, 1971, PATHOLOGY, V3, P233
[2]
Muscle satellite cells are multipotential stem cells that exhibit myogenic, osteogenic, and adipogenic differentiation [J].
Asakura, A ;
Komaki, M ;
Rudnicki, MA .
DIFFERENTIATION, 2001, 68 (4-5) :245-253
[3]
Signaling Gradients during Paraxial Mesoderm Development [J].
Aulehla, Alexander ;
Pourquie, Olivier .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2010, 2 (02) :a000869
[4]
Dystroglycanopathy muscles lacking functional glycosylation of alpha-dystroglycan retain regeneration capacity [J].
Awano, Hiroyuki ;
Blaeser, Anthony ;
Wu, Bo ;
Lu, Pei ;
Keramaris-Vrantsis, Elizabeth ;
Lu, Qi .
NEUROMUSCULAR DISORDERS, 2015, 25 (06) :474-484
[5]
Expression of myosin heavy chain and of myogenic regulatory factor genes in fast or slow rabbit muscle satellite cell cultures [J].
Barjot, C ;
Cotten, ML ;
Goblet, C ;
Whalen, RG ;
Bacou, F .
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 1995, 16 (06) :619-628
[6]
Expression of CD34 and Myf5 defines the majority of quiescent adult skeletal muscle satellite cells [J].
Beauchamp, JR ;
Heslop, L ;
Yu, DSW ;
Tajbakhsh, S ;
Kelly, RG ;
Wernig, A ;
Buckingham, ME ;
Partridge, TA ;
Zammit, PS .
JOURNAL OF CELL BIOLOGY, 2000, 151 (06) :1221-1233
[7]
The emerging biology of muscle stem cells: Implications for cell-based therapies [J].
Bentzinger, C. Florian ;
Wang, Yu Xin ;
von Maltzahn, Julia ;
Rudnicki, Michael A. .
BIOESSAYS, 2013, 35 (03) :231-241
[8]
Building Muscle: Molecular Regulation of Myogenesis [J].
Bentzinger, C. Florian ;
Wang, Yu Xin ;
Rudnicki, Michael A. .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2012, 4 (02)
[9]
p38 MAPK signaling underlies a cell-autonomous loss of stem cell self-renewal in skeletal muscle of aged mice [J].
Bernet, Jennifer D. ;
Doles, Jason D. ;
Hall, John K. ;
Tanaka, Kathleen Kelly ;
Carter, Thomas A. ;
Olwin, Bradley B. .
NATURE MEDICINE, 2014, 20 (03) :265-271
[10]
Heterogeneity in the muscle satellite cell population [J].
Biressi, Stefano ;
Rando, Thomas A. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2010, 21 (08) :845-854