Expression and neural control of follistatin versus myostatin genes during regeneration of mouse soleus

被引:35
作者
Armand, AS
Della Gaspera, B
Launay, T
Charbonnier, F
Gallien, CL
Chanoine, C
机构
[1] Univ Paris 05, Ctr Univ St Peres, Lab Biol Dev & Differenciat Neuromusculaire, CNRS,LNRS ESA 7060, F-75720 Paris 06, France
[2] Univ Paris 05, UFR STAPS, Paris, France
[3] Univ Evry, Dept STAPS, Evry, France
关键词
follistatin; myostatin; muscle regeneration; denervation;
D O I
10.1002/dvdy.10306
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Follistatin and myostatin are two secreted proteins involved in the control of muscle mass during development. These two proteins have opposite effects on muscle growth, as documented by genetic models. The aims of this work were to analyze in mouse, by using in situ hybridization, the spatial and temporal expression patterns of follistatin and myostatin mRNAs during soleus regeneration after cardiotoxin injury, and to investigate the influence of innervation on the accumulation of these two transcripts. Follistatin transcripts could be detected in activated satellite cells as early as the first stages of regeneration and were transiently expressed in forming myotubes. In contrast, myostatin mRNAs accumulated persistently throughout the regeneration process as well as in adult control soleus. Denervation significantly affected both follistatin and myostatin transcript accumulation, but in opposite ways. Muscle denervation persistently reduced the levels of myostatin transcripts as early as the young myotube stage, whereas the levels of follistatin mRNA were strongly increased in the small myotubes in the late stages of regeneration. These results are discussed with regard to the potential functions of both follistatin, as a positive regulator of muscle differentiation, and myostatin, as a negative regulator of skeletal muscle growth. We suggest that the belated up-regulation of the follistatin mRNA level in the small myotubes of the regenerating soleus as well as the down-regulation of the myostatin transcript level after denervation contribute to the differentiation process in denervated regenerating muscle. Developmental Dynamics 227.256-265, 2003. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:256 / 265
页数:10
相关论文
共 37 条
[1]   ADAPTATION OF NICOTINIC ACETYLCHOLINE-RECEPTOR, MYOGENIN, AND MRF4 GENE-EXPRESSION TO LONG-TERM MUSCLE DENERVATION [J].
ADAMS, L ;
CARLSON, BM ;
HENDERSON, L ;
GOLDMAN, D .
JOURNAL OF CELL BIOLOGY, 1995, 131 (05) :1341-1349
[2]   Follistatin regulates bone morphogenetic protein-7 (BMP-7) activity to stimulate embryonic muscle growth [J].
Amthor, H ;
Christ, B ;
Rashid-Doubell, F ;
Kemp, CF ;
Lang, E ;
Patel, K .
DEVELOPMENTAL BIOLOGY, 2002, 243 (01) :115-127
[3]   The expression and regulation of follistatin and a follistatin-like gene during avian somite compartmentalization and myogenesis [J].
Amthor, H ;
Connolly, D ;
Patel, K ;
BrandSaberi, B ;
Wilkinson, DG ;
Cooke, J ;
Christ, B .
DEVELOPMENTAL BIOLOGY, 1996, 178 (02) :343-362
[4]   REGENERATION OF MUSCLES AFTER CARDIOTOXIN INJURY .1. CYTOLOGICAL ASPECTS [J].
COUTEAUX, R ;
MIRA, JC ;
DALBIS, A .
BIOLOGY OF THE CELL, 1988, 62 (02) :171-182
[5]   DETECTION OF MESSENGER-RNAS IN SEA-URCHIN EMBRYOS BY INSITU HYBRIDIZATION USING ASYMMETRIC RNA PROBES [J].
COX, KH ;
DELEON, DV ;
ANGERER, LM ;
ANGERER, RC .
DEVELOPMENTAL BIOLOGY, 1984, 101 (02) :485-502
[6]   The generation and interpretation of positional information within the vertebrate myotome [J].
Currie, PD ;
Ingham, PW .
MECHANISMS OF DEVELOPMENT, 1998, 73 (01) :3-21
[7]   REGENERATION AFTER CARDIOTOXIN INJURY OF INNERVATED AND DENERVATED SLOW AND FAST MUSCLES OF MAMMALS - MYOSIN ISOFORM ANALYSIS [J].
DALBIS, A ;
COUTEAUX, R ;
JANMOT, C ;
ROULET, A ;
MIRA, JC .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 174 (01) :103-110
[8]   EXPRESSION OF A SINGLE TRANSFECTED CDNA CONVERTS FIBROBLASTS TO MYOBLASTS [J].
DAVIS, RL ;
WEINTRAUB, H ;
LASSAR, AB .
CELL, 1987, 51 (06) :987-1000
[9]   IDENTIFICATION OF SKELETAL-MUSCLE PRECURSOR CELLS INVIVO BY USE OF MYOD1 AND MYOGENIN PROBES [J].
GROUNDS, MD ;
GARRETT, KL ;
LAI, MC ;
WRIGHT, WE ;
BEILHARZ, MW .
CELL AND TISSUE RESEARCH, 1992, 267 (01) :99-104
[10]  
HUGHES SM, 1993, DEVELOPMENT, V118, P1137