ACIDIC AND BASIC FIBROBLAST GROWTH-FACTOR MESSENGER-RNAS ARE EXPRESSED BY SKELETAL-MUSCLE SATELLITE CELLS

被引：79
作者：
ALTERIO, J
COURTOIS, Y
ROBELIN, J
BECHET, D
MARTELLY, I
机构：
[1] INSERM,U118,UNITE RECH GERONTOL 118,RUE WHILHEM,F-75016 PARIS,FRANCE
[2] INRA,F-63122 CEYRAT,FRANCE
[3] UNIV PARIS 12,MYOGENESE & REGENERAT MUSCULAIRE LAB,F-94010 CRETEIL,FRANCE
来源：
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 1990年 / 166卷 / 03期
关键词：
D O I：
10.1016/0006-291X(90)90994-X
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
We postulated that Fibroblast Growth Factor (FGF) involved in fetal or regenerative morphogenesis of skeletal muscle originated from this tissue. Using a bovine retina cDNA probe encoding acidic FGF, we showed that growing muscles from bovine fetuses express this mRNA, but that this expression is reduced in neonate muscles. Cultures of proliferating satellite cells isolated from adult rat muscles expressed aFGF mRNA strongly but bFGF mRNA weakly; these mRNAs disappeared in cells differentiated into myotubes. 10-7M 12-O-tetradecanoyl phorbol -13-acetate (TPA) increased aFGF mRNA expression in both proliferating and differentiated satellite cells. Contrastingly, proliferating L6 myogenic cells only expressed aFGF mRNA significantly under TPA treatment. Therefore, the satellite cells did seem to be a possible source for FGF, especially aFGF, which might regulate the myogenic process. © 1990.
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页码：1205 / 1212
页数：8
相关论文
共 35 条
[1]   NUCLEOTIDE-SEQUENCE OF A BOVINE CLONE ENCODING THE ANGIOGENIC PROTEIN, BASIC FIBROBLAST GROWTH-FACTOR [J].
ABRAHAM, JA ;
MERGIA, A ;
WHANG, JL ;
TUMOLO, A ;
FRIEDMAN, J ;
HJERRILD, KA ;
GOSPODAROWICZ, D ;
FIDDES, JC .
SCIENCE, 1986, 233 (4763) :545-548
[2]  
ALLEN RE, 1985, IN VITRO CELL DEV B, V21, P636
[3]   REGULATION OF SKELETAL-MUSCLE SATELLITE CELL-PROLIFERATION BY BOVINE PITUITARY FIBROBLAST GROWTH-FACTOR [J].
ALLEN, RE ;
DODSON, MV ;
LUITEN, LS .
EXPERIMENTAL CELL RESEARCH, 1984, 152 (01) :154-160
[4]   CHARACTERIZATION OF A BOVINE ACIDIC FGF CDNA CLONE AND ITS EXPRESSION IN BRAIN AND RETINA [J].
ALTERIO, J ;
HALLEY, C ;
BROU, C ;
SOUSSI, T ;
COURTOIS, Y ;
LAURENT, M .
FEBS LETTERS, 1988, 242 (01) :41-46
[5]  
BEGUINOT F, 1985, J BIOL CHEM, V260, P5892
[6]   BINDING, INTERNALIZATION, AND DEGRADATION OF BASIC FIBROBLAST GROWTH-FACTOR IN HUMAN MICROVASCULAR ENDOTHELIAL-CELLS [J].
BIKFALVI, A ;
DUPUY, E ;
INYANG, AL ;
FAYEIN, N ;
LESECHE, G ;
COURTOIS, Y ;
TOBELEM, G .
EXPERIMENTAL CELL RESEARCH, 1989, 181 (01) :75-84
[7]   EXPRESSION OF FIBROBLAST GROWTH-FACTOR BY F9 TERATOCARCINOMA CELLS AS A FUNCTION OF DIFFERENTIATION [J].
BRAUNHUT, SJ ;
GUDAS, LJ ;
KUROKAWA, T ;
SASSE, J ;
DAMORE, PA .
JOURNAL OF CELL BIOLOGY, 1989, 108 (06) :2467-2476
[8]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[9]   GROWTH-FACTOR CONTROL OF SKELETAL-MUSCLE DIFFERENTIATION - COMMITMENT TO TERMINAL DIFFERENTIATION OCCURS IN G1 PHASE AND IS REPRESSED BY FIBROBLAST GROWTH-FACTOR [J].
CLEGG, CH ;
LINKHART, TA ;
OLWIN, BB ;
HAUSCHKA, SD .
JOURNAL OF CELL BIOLOGY, 1987, 105 (02) :949-956
[10]   FIBROBLAST GROWTH-FACTOR IN THE EXTRACELLULAR-MATRIX OF DYSTROPHIC (MDX) MOUSE MUSCLE [J].
DIMARIO, J ;
BUFFINGER, N ;
YAMADA, S ;
STROHMAN, RC .
SCIENCE, 1989, 244 (4905) :688-690
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