Muscle satellite cells are multipotential stem cells that exhibit myogenic, osteogenic, and adipogenic differentiation

被引:656
作者
Asakura, A
Komaki, M
Rudnicki, MA
机构
[1] Ottawa Hlth Res Inst, Program Mol Med, Ottawa, ON K1H 8L6, Canada
[2] Univ Toronto, CIHR Periodontal Physiol, Fac Dent, Toronto, ON M5S 3E2, Canada
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
satellite cell; stem cell; MyoD; myogenesis; osteogenesis; adipogenesis; differentiation;
D O I
10.1046/j.1432-0436.2001.680412.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Muscle satellite cells are believed to represent a committed stem cell population that is responsible for the postnatal growth and regeneration of skeletal muscle. However, the observation that cultured myoblasts differentiate into osteocytes or adipocytes following treatment with bone morphogenetic proteins (BMPs) or adipogenic inducers, respectively, suggests some degree of plasticity within the mesenchymal lineage. To further investigate this phenomenon, we explore the osteogenic and adipogenic potential of satellite cells isolated from adult mice. Our experiments clearly demonstrate that satellite cell-derived primary myoblasts, expressing myogenic markers such as MyoD, Myf5, Pax7 and desmin, differentiated only into osteocytes or adipocytes following treatment with BMPs or adipogenic inducers, respectively. However, satellite cells on isolated muscle fibers cultured in Matrigel readily differentiated into myocytes as well as osteogenic and adipogenic lineages, whereas primary myoblasts did not. Satellite cell-derived primary myoblasts isolated from mice lacking the myogenic transcription factor MyoD (MyoD-/-) differentiate into myocytes poorly in vivo and in vitro (Megeney et al., Genes Dev. 1996; Sabourin et. al, J. Cell Biol., 1999). Therefore, we tested whether MyoD-/- primary myoblasts display increased plasticity relative to wild type cells. Unexpectedly, the osteogenic or adipogenic differentiation potential of MyoD-/- primary myoblasts did not increase compared to wild-type cells. Taken together, these results strongly suggest that muscle satellite cells possess multipotential mesenchymal stem cell activity and are capable of forming osteocytes and adipocytes as well as myocytes.
引用
收藏
页码:245 / 253
页数:9
相关论文
共 49 条
[1]
Human osteogenic protein-1 induces chondroblastic, osteoblastic, and/or adipocytic differentiation of clonal murine target cells [J].
Asahina, I ;
Sampath, TK ;
Hauschka, PV .
EXPERIMENTAL CELL RESEARCH, 1996, 222 (01) :38-47
[2]
THE REGULATION OF MYOD GENE-EXPRESSION - CONSERVED ELEMENTS MEDIATE EXPRESSION IN EMBRYONIC AXIAL MUSCLE [J].
ASAKURA, A ;
LYONS, GE ;
TAPSCOTT, SJ .
DEVELOPMENTAL BIOLOGY, 1995, 171 (02) :386-398
[3]
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
[4]
BrandSaberi B, 1996, INT J DEV BIOL, V40, P411
[5]
Cooper RN, 1999, J CELL SCI, V112, P2895
[6]
Single-cell analysis of regulatory gene expression in quiescent and activated mouse skeletal muscle satellite cells [J].
Cornelison, DDW ;
Wold, BJ .
DEVELOPMENTAL BIOLOGY, 1997, 191 (02) :270-283
[7]
MyoD-/- satellite cells in single-fiber culture are differentiation defective and MRF4 deficient [J].
Cornelison, DDW ;
Olwin, BB ;
Rudnicki, MA ;
Wold, BJ .
DEVELOPMENTAL BIOLOGY, 2000, 224 (02) :122-137
[8]
FATAL INFANTILE MITOCHONDRIAL MYOPATHY AND RENAL DYSFUNCTION DUE TO CYTOCHROME-C-OXIDASE DEFICIENCY [J].
DIMAURO, S ;
MENDELL, JR ;
SAHENK, Z ;
BACHMAN, D ;
SCARPA, A ;
SCOFIELD, RM ;
REINER, C .
NEUROLOGY, 1980, 30 (08) :795-804
[9]
Osf2/Cbfa1: A transcriptional activator of osteoblast differentiation [J].
Ducy, P ;
Zhang, R ;
Geoffroy, V ;
Ridall, AL ;
Karsenty, G .
CELL, 1997, 89 (05) :747-754
[10]
Expression of specific white adipose tissue genes in denervation-induced skeletal muscle fatty degeneration [J].
Dulor, JP ;
Cambon, B ;
Vigneron, P ;
Reyne, Y ;
Nouguès, J ;
Casteilla, L ;
Bacou, F .
FEBS LETTERS, 1998, 439 (1-2) :89-92