Cultured myf5 null and myoD null muscle precursor cells display distinct growth defects

被引:48
作者
Montarras, D [1 ]
Lindon, C [1 ]
Pinset, C [1 ]
Domeyne, P [1 ]
机构
[1] Inst Pasteur, Lab Dev Cellulaire, URA 1947, F-75724 Paris 15, France
关键词
myf-5; myoD; muscle; regeneration; proliferation;
D O I
10.1016/S0248-4900(00)01110-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Myf-5 and MyoD are the two muscle regulatory factors expressed from the myoblast stage to maintain the identity and to promote the subsequent differentiation of muscle precursor cells. To get insight into their role we have studied the capacity to proliferate and to differentiate of myf-5 and myoD null myoblasts in primary cultures and in the subsequent passages. Our results indicate that myf-5 null myoblasts differ from wild type (wt) myoblasts in that they undergo precocious differentiation: they become myogenin- and troponin T-positive and fail to incorporate bromodeoxyuridine (BrdU) under culture conditions and at a time when wt cells are not yet differentiated and continue to proliferate. In primary cultures of myoD null cells, up to 60% of the cells were scored as myoblasts on the basis of the expression of myf-5. These myoD-deficient myoblasts, unlike myoD-expressing cells, were poorly differentiating and displayed a severe growth defect that led to their elimination from the cultures: within a few passages myoblasts were absent from myoD-deficient cultures, which mostly consisted of senescent cells. That a null mutation in either gene reduces the proliferative potential of cultured myoblasts raises the possibility that Myf-5 and MyoD serve proliferation of muscle precursor cells. (C) 2000 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:565 / 572
页数:8
相关论文
共 27 条
[1]   Muscle differentiation: more complexity to the network of myogenic regulators [J].
Arnold, HH ;
Winter, B .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1998, 8 (05) :539-544
[2]  
Bischoff R, 1994, MYOLOGY, P97
[3]   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
[4]   MYOD INDUCES GROWTH ARREST INDEPENDENT OF DIFFERENTIATION IN NORMAL AND TRANSFORMED-CELLS [J].
CRESCENZI, M ;
FLEMING, TP ;
LASSAR, AB ;
WEINTRAUB, H ;
AARONSON, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (21) :8442-8446
[5]   A BIOMARKER THAT IDENTIFIES SENESCENT HUMAN-CELLS IN CULTURE AND IN AGING SKIN IN-VIVO [J].
DIMRI, GP ;
LEE, XH ;
BASILE, G ;
ACOSTA, M ;
SCOTT, C ;
ROSKELLEY, C ;
MEDRANO, EE ;
LINSKENS, M ;
RUBELJ, I ;
PEREIRASMITH, O ;
PEACOCKE, M ;
CAMPISI, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9363-9367
[6]   Two domains of MyoD mediate transcriptional activation of genes in repressive chromatin: A mechanism for lineage determination in myogenesis [J].
Gerber, AN ;
Klesert, TR ;
Bergstrom, DA ;
Tapscott, SJ .
GENES & DEVELOPMENT, 1997, 11 (04) :436-450
[7]  
Kablar B, 1997, DEVELOPMENT, V124, P4729
[8]   Myf-5 revisited:: Loss of early myotome formation does not lead to a rib phenotype in homozygous Myf-5 mutant mice [J].
Kaul, A ;
Köster, M ;
Neuhaus, H ;
Braun, T .
CELL, 2000, 102 (01) :17-19
[9]   The muscle regulatory factors MyoD and Myf-5 undergo distinct cell cycle-specific expression in muscle cells [J].
Kitzmann, M ;
Carnac, G ;
Vandromme, M ;
Primig, M ;
Lamb, NJC ;
Fernandez, A .
JOURNAL OF CELL BIOLOGY, 1998, 142 (06) :1447-1459
[10]   Cell cycle-regulated expression of the muscle determination factor Myf5 in proliferating myoblasts [J].
Lindon, C ;
Montarras, D ;
Pinset, C .
JOURNAL OF CELL BIOLOGY, 1998, 140 (01) :111-118