Twist induces reversal of myotube formation

被引:32
作者
Hjiantoniou, Eleni [1 ]
Anayasa, Mustafa [1 ]
Nicolaou, Paschalis [1 ]
Bantounas, Ioannis [2 ]
Saito, Masahiro [3 ]
Iseki, Sachiko [4 ]
Uney, James B. [2 ]
Phylactou, Leonidas A. [1 ]
机构
[1] Cyprus Inst Neurol & Genet, CY-1683 Nicosia, Cyprus
[2] Univ Bristol, Henry Wellcome Labs Integrat Neurosci & Endocrino, Bristol BS1 3NY, Avon, England
[3] Osaka Univ, Dept Mol & Cellular Biochem, Grad Sch Dent, Suita, Osaka 5650871, Japan
[4] Tokyo Med & Dent Univ, Grad Sch, Sec Mol Craniofacial Embryol, Tokyo 1138549, Japan
基金
英国惠康基金;
关键词
twist; myotubes; reversal of differentiation;
D O I
10.1111/j.1432-0436.2007.00195.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
Mammals possess reduced ability to regenerate lost tissue, compared with other vertebrates, which can regenerate through differentiation of precursor cells or de-differentiation. Mammalian multinucleated myotube formation is a differentiation process, which arises from the fusion of mononucleated myoblasts and is thought to be an irreversible process toward muscle formation. By overexpressing the Twist gene in terminally differentiated myotubes, we managed to induce reversal of cell differentiation. More specifically, following expression of the Twist gene, myotubes underwent morphological changes that caused them to cleave. This was accompanied by a reduction in the expression of certain myogenic markers. Interestingly, Twist overexpression also caused a reduction in the muscle transcription factor MyoD. Further experiments showed an increase in the cell cycle entry molecule, cyclin D1 and initiation of DNA synthesis, due to Twist overexpression. The exploitation of Twist-mediated reversal of differentiation and the study of its specific mechanism would be important in order to study mammalian cellular de-differentiation and determine its potential in muscle regeneration.
引用
收藏
页码:182 / 192
页数:11
相关论文
共 35 条
[1]
Myogenin expression, cell cycle withdrawal, and phenotypic differentiation are temporally separable events that precede cell fusion upon myogenesis [J].
Andres, V ;
Walsh, K .
JOURNAL OF CELL BIOLOGY, 1996, 132 (04) :657-666
[2]
BATE M, 1991, DEVELOPMENT, V113, P79
[3]
Twist is substrate for caspase cleavage and proteasome-mediated degradation [J].
Demontis, S ;
Rigo, C ;
Piccinin, S ;
Mizzau, M ;
Sonego, M ;
Fabris, M ;
Brancolini, C ;
Maestro, R .
CELL DEATH AND DIFFERENTIATION, 2006, 13 (02) :335-345
[4]
Insulin-like growth factor 1 (IGF-1)-induced Twist expression is involved in the anti-apoptotic effects of the IGF-1 receptor [J].
Dupont, J ;
Fernandez, AM ;
Glackin, CA ;
Helman, L ;
LeRoith, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (28) :26699-26707
[5]
Mechanisms of muscle dedifferentiation during regeneration [J].
Echeverri, K ;
Tanaka, EM .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2002, 13 (05) :353-360
[6]
ElGhouzzi V, 1997, NAT GENET, V15, P42
[7]
B-LINEAGE SPECIFIC INTERACTIONS OF AN IMMUNOGLOBULIN ENHANCER WITH CELLULAR FACTORS INVIVO [J].
EPHRUSSI, A ;
CHURCH, GM ;
TONEGAWA, S ;
GILBERT, W .
SCIENCE, 1985, 227 (4683) :134-140
[8]
FUCHTBAUER EM, 1995, DEV DYNAM, V204, P316
[9]
Twist protein in mouse embryogenesis [J].
Gitelman, I .
DEVELOPMENTAL BIOLOGY, 1997, 189 (02) :205-214
[10]
Adenoviral-mediated, high-level, cell-specific transgene expression:: A SYN1-WPRE cassette mediates increased transgene expression with no loss of neuron specificity [J].
Glover, CPJ ;
Bienemann, AS ;
Heywood, DJ ;
Cosgrave, AS ;
Uney, JB .
MOLECULAR THERAPY, 2002, 5 (05) :509-516